| geneid | 255967 |
|---|---|
| ensemblid | ENSG00000152520.14 |
| hgncid | 29991 |
| symbol | PAN3 |
| name | poly(A) specific ribonuclease subunit PAN3 |
| refseq_nuc | NM_175854.8 |
| refseq_prot | NP_787050.6 |
| ensembl_nuc | ENST00000380958.8 |
| ensembl_prot | ENSP00000370345.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 28138545 |
| end | 28295335 |
| strand | + |
| ver | v1.2 |
| region | chr13:28138545-28295335 |
| region5000 | chr13:28133545-28300335 |
| regionname0 | PAN3_chr13_28138545_28295335 |
| regionname5000 | PAN3_chr13_28133545_28300335 |
| 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 | 887 | 250 | 79 | 34 | 108 | 2 | 25 | 80 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0002 | 0/0 | 887 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0003 | 0/0 | 887 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| 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 | 1/1 | 2664 | 238 | 71 | 31 | 107 | 2 | 25 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| c0002 | 0/0 | 2664 | 5 | 4 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| c0003 | 0/0 | 2664 | 3 | 3 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| c0004 | 0/0 | 2664 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| c0005 | 0/0 | 2664 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| c0006 | 0/0 | 2664 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| c0007 | 0/0 | 2664 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| c0008 | 0/0 | 2664 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| c0009 | 0/0 | 2664 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| 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 | 0/0 | 2923 | 73 | 14 | 7 | 40 | 0 | 12 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0002 | 0/0 | 2943 | 33 | 3 | 1 | 28 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0003 | 0/0 | 2944 | 21 | 7 | 4 | 10 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0004 | 0/1 | 2924 | 20 | 2 | 5 | 9 | 0 | 3 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0005 | 0/0 | 2937 | 12 | 4 | 2 | 3 | 1 | 2 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0006 | 0/0 | 2927 | 9 | 2 | 5 | 0 | 0 | 2 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0007 | 0/0 | 2938 | 7 | 1 | 2 | 2 | 0 | 2 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0008 | 0/0 | 2942 | 6 | 5 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0009 | 0/0 | 2942 | 6 | 2 | 0 | 4 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0010 | 0/0 | 2934 | 5 | 5 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0011 | 0/0 | 2936 | 3 | 3 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0012 | 0/0 | 2937 | 3 | 3 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0013 | 0/0 | 2923 | 3 | 2 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0014 | 0/0 | 2927 | 3 | 3 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0015 | 0/0 | 2938 | 2 | 2 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0016 | 0/0 | 2934 | 2 | 0 | 0 | 1 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0017 | 0/0 | 2936 | 2 | 2 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0018 | 0/0 | 2936 | 2 | 1 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0019 | 0/0 | 2937 | 2 | 2 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0020 | 0/0 | 2933 | 2 | 0 | 0 | 2 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0021 | 0/0 | 2948 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0022 | 0/0 | 2945 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0023 | 0/0 | 2937 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0024 | 0/0 | 2938 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0025 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0026 | 0/0 | 2932 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0027 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0028 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0029 | 0/0 | 2936 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0030 | 0/0 | 2936 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0031 | 0/0 | 2945 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0032 | 0/0 | 2937 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0033 | 0/0 | 2948 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0034 | 0/0 | 2942 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0035 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0036 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0037 | 0/0 | 2945 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0038 | 0/0 | 2957 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0039 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0040 | 0/0 | 2936 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0041 | 0/0 | 2937 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0042 | 0/0 | 2937 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0043 | 0/0 | 2927 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0044 | 0/0 | 2924 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0045 | 0/0 | 2927 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0046 | 0/0 | 2923 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0047 | 0/0 | 2949 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0048 | 0/0 | 2923 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0049 | 0/0 | 2932 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0050 | 0/0 | 2923 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0051 | 0/0 | 2924 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0052 | 0/0 | 2936 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0053 | 0/0 | 2924 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0054 | 1/0 | 2927 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0055 | 0/0 | 2923 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| t0056 | 0/0 | 2924 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| 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 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| 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 | 1/1 | 2664 | 238 | 71 | 31 | 107 | 2 | 25 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0002 | 0/0 | 2664 | 5 | 4 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0003 | 0/0 | 2664 | 3 | 3 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0004 | 0/0 | 2664 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0007 | 0/0 | 2664 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0008 | 0/0 | 2664 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0009 | 0/0 | 2664 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0002c0005 | 0/0 | 2664 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0003c0006 | 0/0 | 2664 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5586 | 69 | 13 | 6 | 39 | 0 | 11 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0002 | 0/0 | 5606 | 33 | 3 | 1 | 28 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0003 | 0/0 | 5607 | 21 | 7 | 4 | 10 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0004 | 0/1 | 5587 | 18 | 1 | 4 | 9 | 0 | 3 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0005 | 0/0 | 5600 | 12 | 4 | 2 | 3 | 1 | 2 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0006 | 0/0 | 5590 | 9 | 2 | 5 | 0 | 0 | 2 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0007 | 0/0 | 5601 | 7 | 1 | 2 | 2 | 0 | 2 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0008 | 0/0 | 5605 | 6 | 5 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0009 | 0/0 | 5605 | 6 | 2 | 0 | 4 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0010 | 0/0 | 5597 | 5 | 5 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0011 | 0/0 | 5599 | 3 | 3 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0013 | 0/0 | 5586 | 3 | 2 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0014 | 0/0 | 5590 | 2 | 2 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0015 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0016 | 0/0 | 5597 | 2 | 0 | 0 | 1 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0017 | 0/0 | 5599 | 2 | 2 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0019 | 0/0 | 5600 | 2 | 2 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0020 | 0/0 | 5596 | 2 | 0 | 0 | 2 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0022 | 0/0 | 5608 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0023 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0024 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0025 | 0/0 | 5601 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0026 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0027 | 0/0 | 5598 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0028 | 0/0 | 5598 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0029 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0030 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0031 | 0/0 | 5608 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0032 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0033 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0034 | 0/0 | 5605 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0035 | 0/0 | 5606 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0036 | 0/0 | 5598 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0037 | 0/0 | 5608 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0038 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0039 | 0/0 | 5598 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0040 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0041 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0042 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0043 | 0/0 | 5590 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0044 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0045 | 0/0 | 5590 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0046 | 0/0 | 5586 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0047 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0048 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0049 | 0/0 | 5595 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0050 | 0/0 | 5586 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0051 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0052 | 0/0 | 5599 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0053 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0054 | 1/0 | 5590 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0055 | 0/0 | 5586 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0001t0056 | 0/0 | 5587 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0002t0012 | 0/0 | 5600 | 3 | 3 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0002t0018 | 0/0 | 5599 | 2 | 1 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0003t0001 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0003t0004 | 0/0 | 5587 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0003t0014 | 0/0 | 5590 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0004t0004 | 0/0 | 5587 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0007t0021 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0008t0001 | 0/0 | 5586 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0001c0009t0001 | 0/0 | 5586 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0002c0005t0001 | 0/0 | 5586 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| a0003c0006t0015 | 0/0 | 5601 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | copy fasta | chr13 | 28133545 | 28300335 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0009g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0011g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0013g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0013g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0014g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0014g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0015g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0016g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0016g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0017g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0017g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0019g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0019g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0020g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0020g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0022g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0023g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0024g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0025g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0026g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0027g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0028g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0029g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0030g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0031g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0032g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0033g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0034g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0035g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0036g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0037g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0038g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0039g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0040g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0041g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0042g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0043g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0044g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0045g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0046g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0047g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0048g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0049g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0050g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0051g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0052g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0053g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0054g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0055g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0001t0056g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0002t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0002t0012g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0002t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0002t0018g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0002t0018g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0003t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0003t0014g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0004t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0007t0021g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0008t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0001c0009t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0002c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| a0003c0006t0015g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0176 | EUR | GBR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00099 | hp2 | a0001 | c0001 | t0013 | g0015 | EUR | GBR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0207 | EAS | CHS | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0206 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0188 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0031 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG00735 | hp2 | a0001 | c0001 | t0026 | g0239 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0133 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0137 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01099 | hp1 | a0001 | c0001 | t0027 | g0150 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01109 | hp1 | a0001 | c0002 | t0018 | g0212 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0177 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01175 | hp2 | a0001 | c0001 | t0056 | g0087 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0030 | AMR | PUR | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0065 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01346 | hp2 | a0001 | c0001 | t0045 | g0102 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01358 | hp2 | a0001 | c0001 | t0025 | g0203 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01361 | hp1 | a0001 | c0001 | t0022 | g0228 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01361 | hp2 | a0001 | c0004 | t0004 | g0064 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0178 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0104 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0247 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0124 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02004 | hp2 | a0001 | c0008 | t0001 | g0068 | AMR | PEL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02040 | hp2 | a0001 | c0001 | t0053 | g0046 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0220 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02132 | hp1 | a0001 | c0001 | t0050 | g0050 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02135 | hp2 | a0001 | c0001 | t0051 | g0095 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02145 | hp1 | a0001 | c0001 | t0024 | g0226 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | CDX | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02165 | hp2 | a0001 | c0001 | t0034 | g0193 | EAS | CDX | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0111 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02257 | hp2 | a0001 | c0001 | t0041 | g0006 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0204 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02258 | hp2 | a0001 | c0001 | t0038 | g0243 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02572 | hp1 | a0001 | c0001 | t0017 | g0205 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02572 | hp2 | a0001 | c0001 | t0042 | g0186 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02602 | hp1 | a0001 | c0001 | t0043 | g0252 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02602 | hp2 | a0002 | c0005 | t0001 | g0132 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02615 | hp2 | a0001 | c0001 | t0047 | g0019 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02717 | hp1 | a0001 | c0001 | t0032 | g0225 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02723 | hp2 | a0001 | c0001 | t0039 | g0005 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0152 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02809 | hp2 | a0001 | c0001 | t0030 | g0161 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02886 | hp1 | a0001 | c0001 | t0019 | g0238 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0246 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0122 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0121 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0245 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02922 | hp1 | a0001 | c0003 | t0014 | g0078 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0174 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02965 | hp2 | a0001 | c0007 | t0021 | g0151 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02970 | hp2 | a0001 | c0002 | t0012 | g0211 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0160 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03017 | hp1 | a0001 | c0001 | t0016 | g0196 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0248 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03098 | hp1 | a0001 | c0001 | t0029 | g0249 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03098 | hp2 | a0001 | c0001 | t0031 | g0223 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0187 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03195 | hp2 | a0001 | c0001 | t0033 | g0123 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0127 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0189 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0033 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03453 | hp1 | a0001 | c0002 | t0012 | g0162 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03453 | hp2 | a0001 | c0001 | t0023 | g0171 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03486 | hp1 | a0001 | c0001 | t0048 | g0018 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03486 | hp2 | a0001 | c0001 | t0040 | g0004 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03516 | hp1 | a0003 | c0006 | t0015 | g0251 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03516 | hp2 | a0001 | c0002 | t0012 | g0209 | AFR | ESN | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0126 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03579 | hp2 | a0001 | c0003 | t0004 | g0135 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0052 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0182 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0116 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0053 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0183 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0090 | SAS | BEB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG04228 | hp1 | a0001 | c0001 | t0055 | g0088 | SAS | STU | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG04228 | hp2 | a0001 | c0001 | t0046 | g0035 | SAS | STU | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18522 | hp1 | a0001 | c0001 | t0052 | g0110 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0184 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18943 | hp2 | a0001 | c0001 | t0009 | g0194 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0208 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18956 | hp2 | a0001 | c0001 | t0016 | g0040 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0237 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18974 | hp2 | a0001 | c0001 | t0035 | g0199 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18981 | hp2 | a0001 | c0001 | t0009 | g0215 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18986 | hp2 | a0001 | c0001 | t0049 | g0154 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18993 | hp2 | a0001 | c0001 | t0044 | g0048 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18998 | hp1 | a0001 | c0001 | t0036 | g0041 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19003 | hp1 | a0001 | c0001 | t0020 | g0190 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0112 | AFR | LWK | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | LWK | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | LWK | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19043 | hp2 | a0001 | c0001 | t0015 | g0250 | AFR | LWK | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19068 | hp2 | a0001 | c0001 | t0020 | g0192 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19078 | hp2 | a0001 | c0009 | t0001 | g0063 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19085 | hp2 | a0001 | c0001 | t0009 | g0198 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19090 | hp2 | a0001 | c0001 | t0037 | g0222 | EAS | JPT | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19240 | hp1 | a0001 | c0002 | t0018 | g0210 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0109 | SAS | GIH | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0181 | SAS | GIH | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02109 | hp1 | a0001 | c0001 | t0019 | g0185 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02109 | hp2 | a0001 | c0001 | t0028 | g0125 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0244 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0242 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0136 | AFR | MSL | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | USA | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0128 | AFR | USA | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | USA | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0057 | REF | REF | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0054 | g0097 | REF | REF | PAN3_chr13_28133545_28300335 | PAN3 | chr13 | 28133545 | 28300335 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:28256402
|
G | A | 1 | a0002 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1111G>A | p.Val371Met | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/19 | 1224/5590 | 1111/2664 | 371/887 | chr13 | 28256402 | ||
| chr13:28270824
|
G | A | 1 | a0003 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.1916G>A | p.Arg639Gln | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/19 | 2029/5590 | 1916/2664 | 639/887 | chr13 | 28270824 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:28138834
|
C | T | 1 | a0001c0009 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.177C>T | p.Phe59Phe | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 290/5590 | 177/2664 | 59/887 | chr13 | 28138834 | ||
| chr13:28138858
|
G | T | 1 | a0001c0008 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.201G>T | p.Leu67Leu | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 314/5590 | 201/2664 | 67/887 | chr13 | 28138858 | ||
| chr13:28220374
|
G | A | 1 | a0001c0004 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.996G>A | p.Ala332Ala | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/19 | 1109/5590 | 996/2664 | 332/887 | chr13 | 28220374 | ||
| chr13:28256299
|
G | A | 1 | a0001c0003 | 3 | HG02922.hp1 HG03471.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.1008G>A | p.Ser336Ser | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/19 | 1121/5590 | 1008/2664 | 336/887 | chr13 | 28256299 | ||
| chr13:28260488
|
C | T | 1 | a0001c0003 | 3 | HG02922.hp1 HG03471.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.1290C>T | p.His430His | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/19 | 1403/5590 | 1290/2664 | 430/887 | chr13 | 28260488 | ||
| chr13:28280520
|
C | A | 1 | a0001c0002 | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
synonymous_variant | LOW | c.2298C>A | p.Val766Val | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/19 | 2411/5590 | 2298/2664 | 766/887 | chr13 | 28280520 | ||
| chr13:28281338
|
T | C | 1 | a0001c0007 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.2343T>C | p.Phe781Phe | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/19 | 2456/5590 | 2343/2664 | 781/887 | chr13 | 28281338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:28138552
|
C | G | 1 | a0001c0001t0056 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 106 | chr13 | 28138552 | |||||
| chr13:28138594
|
C | T | 1 | a0001c0001t0055 | 1 | HG04228.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-64C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | chr13 | 28138594 | ||||||
| chr13:28138603
|
T | TGGCGGCG others(2): Show |
36 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(33): Show | 127 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(124): Show |
5_prime_UTR_variant | MODIFIER | c.-53_-52insCGGCGGCG others(1): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 52 | INFO_REALIGN_3_PRIME | chr13 | 28138603 | ||||
| chr13:28138603
|
T | TGGCGGCG others(5): Show |
1 | a0001c0007t0021 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-53_-52insCGGCGGCG others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 52 | INFO_REALIGN_3_PRIME | chr13 | 28138603 | ||||
| chr13:28138606
|
T | C | 39 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(36): Show | 131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
5_prime_UTR_variant | MODIFIER | c.-52T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/19 | 52 | chr13 | 28138606 | |||||
| chr13:28292549
|
T | TG | 5 | a0001c0001t0011a0001c0001t0019a0001c0001t0042others(2): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*29dupG | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 30 | INFO_REALIGN_3_PRIME | chr13 | 28292549 | ||||
| chr13:28292873
|
T | C | 60 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(57): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*351T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 351 | chr13 | 28292873 | |||||
| chr13:28292876
|
T | C | 1 | a0001c0001t0044 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 354 | chr13 | 28292876 | |||||
| chr13:28292878
|
G | C | 1 | a0001c0001t0022 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*356G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 356 | chr13 | 28292878 | |||||
| chr13:28292921
|
G | A | 2 | a0001c0001t0023a0001c0001t0024 | 2 | HG02145.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*399G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 399 | chr13 | 28292921 | |||||
| chr13:28293005
|
T | C | 1 | a0001c0001t0042 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 483 | chr13 | 28293005 | |||||
| chr13:28293023
|
C | T | 3 | a0001c0001t0017a0001c0001t0023a0001c0001t0024 | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*501C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 501 | chr13 | 28293023 | |||||
| chr13:28293043
|
C | T | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | 237 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*521C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 521 | chr13 | 28293043 | |||||
| chr13:28293108
|
C | T | 2 | a0001c0001t0006a0001c0001t0045 | 10 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*586C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 586 | chr13 | 28293108 | |||||
| chr13:28293121
|
C | G | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(10): Show | 72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*599C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 599 | chr13 | 28293121 | |||||
| chr13:28293131
|
C | T | 18 | a0001c0001t0001a0001c0001t0004a0001c0001t0014others(15): Show | 104 | HG00438.hp1 HG01081.hp1 HG01099.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*609C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 609 | chr13 | 28293131 | |||||
| chr13:28293387
|
G | GT | 4 | a0001c0001t0005a0001c0001t0023a0001c0001t0032others(1): Show | 15 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*894dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 895 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | ||||
| chr13:28293387
|
G | GTT | 5 | a0001c0001t0007a0001c0001t0015a0001c0001t0024others(2): Show | 11 | HG00597.hp2 HG01175.hp1 HG01358.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*893_*894dupTT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 895 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | ||||
| chr13:28293387
|
G | GTTTTTTT others(5): Show |
2 | a0001c0001t0033a0001c0001t0038 | 2 | HG02258.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*883_*894dupTTTTTT others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 895 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | ||||
| chr13:28293387
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0047 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*882_*894dupTTTTTT others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 895 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | ||||
| chr13:28293387
|
GT | G | 7 | a0001c0001t0003a0001c0001t0011a0001c0001t0027others(4): Show | 30 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*894delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 894 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | ||||
| chr13:28293387
|
GTT | G | 4 | a0001c0001t0002a0001c0001t0010a0001c0001t0016others(1): Show | 41 | HG00438.hp2 HG00597.hp1 HG01261.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*893_*894delTT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 893 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | ||||
| chr13:28293387
|
GTTT | G | 10 | a0001c0001t0004a0001c0001t0009a0001c0001t0020others(7): Show | 33 | HG01109.hp2 HG01175.hp2 HG01261.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*892_*894delTTT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 892 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | ||||
| chr13:28293387
|
GTTTT | G | 12 | a0001c0001t0001a0001c0001t0013a0001c0001t0026others(9): Show | 82 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*891_*894delTTTT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 891 | INFO_REALIGN_3_PRIME | chr13 | 28293387 | ||||
| chr13:28293391
|
T | TTTTTTG | 1 | a0001c0001t0008 | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*874_*875insGTTTTT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 875 | INFO_REALIGN_3_PRIME | chr13 | 28293391 | ||||
| chr13:28293415
|
T | G | 1 | a0001c0001t0048 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*893T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 893 | chr13 | 28293415 | |||||
| chr13:28293416
|
T | G | 1 | a0001c0001t0034 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*894T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 894 | chr13 | 28293416 | |||||
| chr13:28293419
|
G | T | 1 | a0001c0001t0032 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*897G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 897 | chr13 | 28293419 | |||||
| chr13:28293421
|
G | C | 3 | a0001c0001t0015a0001c0001t0029a0003c0006t0015 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*899G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 899 | chr13 | 28293421 | |||||
| chr13:28293426
|
G | A | 4 | a0001c0001t0005a0001c0001t0007a0001c0001t0027others(1): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*904G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 904 | chr13 | 28293426 | |||||
| chr13:28293442
|
T | C | 3 | a0001c0001t0015a0001c0001t0029a0003c0006t0015 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*920T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 920 | chr13 | 28293442 | |||||
| chr13:28293455
|
C | T | 2 | a0001c0001t0050a0001c0001t0051 | 2 | HG02132.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*933C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 933 | chr13 | 28293455 | |||||
| chr13:28293581
|
T | G | 1 | a0001c0001t0032 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 1059 | chr13 | 28293581 | |||||
| chr13:28293609
|
T | A | 1 | a0001c0001t0035 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1087T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 1087 | chr13 | 28293609 | |||||
| chr13:28294156
|
G | A | 4 | a0001c0001t0005a0001c0001t0007a0001c0001t0027others(1): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1634G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 1634 | chr13 | 28294156 | |||||
| chr13:28294750
|
G | A | 2 | a0001c0002t0012a0001c0002t0018 | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2228G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 2228 | chr13 | 28294750 | |||||
| chr13:28295010
|
G | GGATATAA others(2): Show |
14 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(11): Show | 72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2489_*2497dupGATA others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 2498 | INFO_REALIGN_3_PRIME | chr13 | 28295010 | ||||
| chr13:28295206
|
A | G | 1 | a0001c0001t0046 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2684A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 2684 | chr13 | 28295206 | |||||
| chr13:28295326
|
C | A | 1 | a0001c0001t0045 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2804C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 19/19 | 2804 | chr13 | 28295326 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:28139118
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0003g0001a0001c0001t0003g0003 | 3 | HG02622.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.430+31G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139118 | ||||||
| chr13:28139135
|
T | A | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.430+48T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139135 | ||||||
| chr13:28139188
|
C | T | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.430+101C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139188 | ||||||
| chr13:28139225
|
C | T | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.430+138C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139225 | ||||||
| chr13:28139505
|
GGGGT | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+420_430+423del others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139505 | |||||
| chr13:28139507
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0008g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430+426_430+427ins others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139507 | |||||
| chr13:28139514
|
T | G | 4 | a0001c0001t0008g0007a0001c0001t0015g0250a0001c0001t0029g0249others(1): Show | 4 | HG03098.hp1 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+427T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139514 | ||||||
| chr13:28139514
|
T | TTG | 32 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0129others(29): Show | 32 | HG00438.hp1 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.430+463_430+464dup others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
T | TTGTG | 12 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(9): Show | 12 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.430+461_430+464dup others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
T | TTGTGTG | 28 | a0001c0001t0002g0002a0001c0001t0002g0164a0001c0001t0002g0166others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.430+459_430+464dup others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
T | TTGTGTGT others(1): Show |
25 | a0001c0001t0001g0213a0001c0001t0002g0191a0001c0001t0002g0195others(22): Show | 25 | HG00597.hp2 HG00639.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.430+457_430+464dup others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
T | TTGTGTGT others(3): Show |
19 | a0001c0001t0002g0217a0001c0001t0002g0219a0001c0001t0002g0221others(16): Show | 19 | HG00438.hp2 HG00597.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+455_430+464dup others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
T | TTGTGTGT others(5): Show |
11 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0002g0236others(8): Show | 11 | HG01261.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+453_430+464dup others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
T | TTGTGTGT others(7): Show |
4 | a0001c0001t0002g0240a0001c0001t0003g0241a0001c0001t0011g0242others(1): Show | 4 | HG00735.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+451_430+464dup others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0008g0244a0001c0001t0038g0243 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.430+449_430+464dup others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
T | TTGTGTGT others(13): Show |
2 | a0001c0001t0008g0245a0001c0001t0008g0246 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.430+445_430+464dup others(20): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
T | TTGTGTGT others(15): Show |
1 | a0001c0001t0008g0247 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.430+443_430+464dup others(22): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
T | TTGTGTGT others(19): Show |
1 | a0001c0001t0008g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.430+439_430+464dup others(26): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
TTG | T | 30 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(27): Show | 30 | HG00099.hp2 HG00735.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.430+463_430+464del others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139514
|
TTGTGTG | T | 5 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0008others(2): Show | 5 | HG02083.hp1 NA18961.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+459_430+464del others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139514 | |||||
| chr13:28139824
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+737A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139824 | ||||||
| chr13:28139845
|
G | A | 2 | a0001c0001t0026g0239a0001c0007t0021g0151 | 2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.430+758G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28139845 | ||||||
| chr13:28139936
|
G | GTGT | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0004g0043others(1): Show | 4 | HG02015.hp1 HG03453.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+875_430+877dup others(3): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139936 | |||||
| chr13:28139936
|
GTGT | G | 3 | a0001c0001t0001g0118a0001c0001t0001g0213a0001c0007t0021g0151 | 3 | HG02015.hp2 HG02965.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.430+875_430+877del others(3): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28139936 | |||||
| chr13:28140022
|
A | C | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+935A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140022 | ||||||
| chr13:28140305
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.430+1218A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140305 | ||||||
| chr13:28140410
|
AAAATAAT others(3): Show |
A | 3 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.430+1325_430+1334d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28140410 | |||||
| chr13:28140413
|
A | G | 2 | a0001c0001t0002g0227a0001c0001t0022g0228 | 2 | HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.430+1326A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140413 | ||||||
| chr13:28140417
|
T | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+1330T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140417 | ||||||
| chr13:28140540
|
G | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18747.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.430+1453G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140540 | ||||||
| chr13:28140672
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+1585A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140672 | ||||||
| chr13:28140687
|
T | TTGTTC | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+1612_430+1616d others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28140687 | |||||
| chr13:28140699
|
G | GTTCTT | 125 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(122): Show | 125 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.430+1617_430+1621d others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28140699 | |||||
| chr13:28140718
|
C | T | 1 | a0001c0001t0005g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.430+1631C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140718 | ||||||
| chr13:28140881
|
A | G | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+1794A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140881 | ||||||
| chr13:28140883
|
C | T | 5 | a0001c0002t0012g0162a0001c0002t0012g0209a0001c0002t0012g0211others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+1796C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140883 | ||||||
| chr13:28140909
|
G | C | 132 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(129): Show | 132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+1822G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140909 | ||||||
| chr13:28140983
|
C | T | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0014g0111others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+1896C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28140983 | ||||||
| chr13:28141003
|
C | CT | 6 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0108others(3): Show | 6 | HG02055.hp2 HG03017.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+1935dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | |||||
| chr13:28141003
|
C | CTTTTTAT others(1): Show |
5 | a0001c0001t0002g0227a0001c0001t0003g0001a0001c0001t0003g0224others(2): Show | 5 | HG01361.hp1 HG02622.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+1921_430+1922i others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | |||||
| chr13:28141003
|
C | CTTTTTT | 9 | a0001c0001t0008g0245a0001c0001t0023g0171a0001c0001t0026g0239others(6): Show | 9 | HG00735.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.430+1930_430+1935d others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | |||||
| chr13:28141003
|
C | CTTTTTTT | 27 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(24): Show | 27 | HG01099.hp1 HG01109.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.430+1929_430+1935d others(9): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | |||||
| chr13:28141003
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0005g0176a0001c0001t0005g0188a0001c0001t0007g0177others(5): Show | 8 | HG00099.hp1 HG00639.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+1928_430+1935d others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | |||||
| chr13:28141003
|
C | CTTTTTTT others(2): Show |
14 | a0001c0001t0005g0179a0001c0001t0005g0180a0001c0001t0005g0181others(11): Show | 14 | HG00597.hp2 HG00639.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.430+1927_430+1935d others(11): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | |||||
| chr13:28141003
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0005g0117 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.430+1926_430+1935d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | |||||
| chr13:28141003
|
CT | C | 6 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0006g0013others(3): Show | 6 | HG01069.hp1 HG02040.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+1935delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141003 | |||||
| chr13:28141006
|
T | TTTATTTT others(1): Show |
9 | a0001c0001t0002g0002a0001c0001t0002g0233a0001c0001t0002g0240others(6): Show | 9 | HG01167.hp2 HG01891.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+1921_430+1922i others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141006 | |||||
| chr13:28141007
|
T | TTATTTTT others(1): Show |
55 | a0001c0001t0001g0213a0001c0001t0002g0010a0001c0001t0002g0012others(52): Show | 55 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.430+1921_430+1922i others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141007 | |||||
| chr13:28141067
|
G | A | 1 | a0001c0001t0003g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.430+1980G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141067 | ||||||
| chr13:28141379
|
C | T | 70 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(67): Show | 70 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.430+2292C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141379 | ||||||
| chr13:28141379
|
CTT | C | 4 | a0001c0001t0005g0179a0001c0001t0005g0206a0001c0001t0007g0178others(1): Show | 4 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2295_430+2296d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141379 | |||||
| chr13:28141456
|
TTTTTTC | T | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+2375_430+2380d others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141456 | |||||
| chr13:28141462
|
C | CT | 35 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0103others(32): Show | 35 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.430+2397dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141462 | |||||
| chr13:28141462
|
C | CTT | 10 | a0001c0001t0002g0170a0001c0001t0002g0236a0001c0001t0005g0208others(7): Show | 10 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.430+2396_430+2397d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141462 | |||||
| chr13:28141462
|
CT | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0129a0001c0001t0002g0191others(5): Show | 8 | HG01099.hp2 HG01167.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+2397delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141462 | |||||
| chr13:28141462
|
CTTTTT | C | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+2393_430+2397d others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141462 | |||||
| chr13:28141462
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0005g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.430+2384_430+2397d others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28141462 | |||||
| chr13:28141468
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0013g0127a0001c0001t0013g0128 | 3 | HG03017.hp2 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.430+2381T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141468 | ||||||
| chr13:28141542
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430+2455A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141542 | ||||||
| chr13:28141702
|
G | C | 18 | a0001c0001t0001g0032a0001c0001t0001g0130a0001c0001t0001g0131others(15): Show | 18 | HG00099.hp2 HG00735.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.430+2615G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141702 | ||||||
| chr13:28141703
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0004g0055 | 2 | HG02165.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.430+2616G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141703 | ||||||
| chr13:28141791
|
A | T | 59 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(56): Show | 59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.430+2704A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141791 | ||||||
| chr13:28141793
|
G | C | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2706G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141793 | ||||||
| chr13:28141806
|
A | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+2719A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28141806 | ||||||
| chr13:28142027
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.430+2940A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142027 | ||||||
| chr13:28142325
|
G | A | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+3238G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142325 | ||||||
| chr13:28142334
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+3247C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142334 | ||||||
| chr13:28142481
|
A | ATGTGTGT others(3): Show |
5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0014g0111others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+3395_430+3404d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142481 | |||||
| chr13:28142511
|
A | AT | 7 | a0001c0001t0001g0029a0001c0001t0001g0100a0001c0001t0001g0119others(4): Show | 7 | HG01071.hp2 HG02015.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+3443dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTT | 6 | a0001c0001t0002g0143a0001c0001t0003g0142a0001c0001t0017g0204others(3): Show | 6 | HG01069.hp2 HG01358.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+3439_430+3443d others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTT | 51 | a0001c0001t0001g0213a0001c0001t0002g0010a0001c0001t0002g0036others(48): Show | 51 | HG00438.hp2 HG00597.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.430+3438_430+3443d others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT | 11 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0200others(8): Show | 11 | HG02135.hp1 HG02895.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+3437_430+3443d others(9): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT others(1): Show |
8 | a0001c0001t0002g0227a0001c0001t0003g0001a0001c0001t0003g0229others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+3436_430+3443d others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0002g0233a0001c0001t0002g0240 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.430+3434_430+3443d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0008g0244a0001c0001t0008g0248 | 2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.430+3433_430+3443d others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0008g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430+3432_430+3443d others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT others(6): Show |
3 | a0001c0001t0008g0245a0001c0001t0008g0246a0001c0001t0008g0247 | 3 | HG01496.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.430+3431_430+3443d others(15): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0010g0152a0001c0001t0033g0123 | 2 | HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.430+3430_430+3443d others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0010g0121 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.430+3429_430+3443d others(17): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0010g0122a0001c0001t0028g0125 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.430+3428_430+3443d others(18): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0010g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+3427_430+3443d others(19): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
A | ATTTTTTT others(12): Show |
1 | a0001c0001t0010g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.430+3425_430+3443d others(21): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
AT | A | 8 | a0001c0001t0001g0056a0001c0001t0003g0141a0001c0001t0005g0172others(5): Show | 8 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+3443delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142511
|
ATT | A | 27 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(24): Show | 27 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.430+3442_430+3443d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28142511 | |||||
| chr13:28142558
|
C | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+3471C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142558 | ||||||
| chr13:28142567
|
C | G | 1 | a0001c0001t0002g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+3480C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142567 | ||||||
| chr13:28142612
|
C | T | 1 | a0001c0001t0002g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+3525C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142612 | ||||||
| chr13:28142774
|
G | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+3687G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142774 | ||||||
| chr13:28142978
|
G | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0139a0001c0001t0004g0099 | 3 | NA18948.hp1 NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.430+3891G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28142978 | ||||||
| chr13:28143114
|
G | T | 2 | a0001c0001t0026g0239a0001c0007t0021g0151 | 2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.430+4027G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143114 | ||||||
| chr13:28143120
|
G | T | 25 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(22): Show | 25 | HG00735.hp2 HG01358.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.430+4033G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143120 | ||||||
| chr13:28143173
|
C | G | 1 | a0001c0001t0033g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.430+4086C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143173 | ||||||
| chr13:28143255
|
G | T | 132 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(129): Show | 132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+4168G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143255 | ||||||
| chr13:28143379
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+4292A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143379 | ||||||
| chr13:28143483
|
T | A | 1 | a0001c0001t0002g0149 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.430+4396T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143483 | ||||||
| chr13:28143533
|
G | A | 2 | a0001c0001t0006g0030a0001c0001t0045g0102 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.430+4446G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143533 | ||||||
| chr13:28143546
|
T | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(1): Show | 4 | HG02602.hp2 HG03669.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+4459T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143546 | ||||||
| chr13:28143832
|
C | T | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+4745C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143832 | ||||||
| chr13:28143874
|
G | A | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.430+4787G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28143874 | ||||||
| chr13:28144027
|
T | C | 250 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(247): Show |
intron_variant | MODIFIER | c.430+4940T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144027 | ||||||
| chr13:28144160
|
G | C | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.430+5073G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144160 | ||||||
| chr13:28144203
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.430+5124_430+5134d others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144203 | |||||
| chr13:28144209
|
TTG | T | 5 | a0001c0001t0008g0007a0001c0001t0008g0245a0001c0001t0008g0246others(2): Show | 5 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+5124_430+5125d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144209 | |||||
| chr13:28144210
|
TG | T | 4 | a0001c0001t0008g0244a0001c0001t0025g0203a0001c0001t0026g0239others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+5124delG | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144210 | ||||||
| chr13:28144211
|
G | GT | 45 | a0001c0001t0001g0026a0001c0001t0001g0089a0001c0001t0001g0091others(42): Show | 45 | HG00438.hp1 HG00597.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.430+5147dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144211 | |||||
| chr13:28144211
|
G | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0003g0232others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+5124G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144211 | ||||||
| chr13:28144211
|
GT | G | 40 | a0001c0001t0002g0164a0001c0001t0005g0172a0001c0001t0005g0173others(37): Show | 40 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.430+5147delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144211 | |||||
| chr13:28144217
|
T | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+5130T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144217 | ||||||
| chr13:28144219
|
T | G | 1 | a0001c0001t0006g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.430+5132T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144219 | ||||||
| chr13:28144220
|
T | G | 6 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+5133T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144220 | ||||||
| chr13:28144222
|
T | G | 2 | a0001c0001t0002g0042a0001c0001t0007g0237 | 2 | NA18960.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.430+5135T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144222 | ||||||
| chr13:28144223
|
T | G | 31 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(28): Show | 31 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.430+5136T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144223 | ||||||
| chr13:28144235
|
G | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+5148G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144235 | ||||||
| chr13:28144416
|
C | T | 1 | a0001c0001t0002g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.430+5329C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144416 | ||||||
| chr13:28144437
|
A | G | 131 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(128): Show | 131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.430+5350A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144437 | ||||||
| chr13:28144438
|
A | T | 1 | a0001c0001t0002g0149 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.430+5351A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144438 | ||||||
| chr13:28144514
|
C | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+5427C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144514 | ||||||
| chr13:28144520
|
C | T | 3 | a0001c0001t0011g0187a0001c0001t0011g0242a0001c0001t0019g0238 | 3 | HG02886.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.430+5433C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144520 | ||||||
| chr13:28144522
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+5435A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144522 | ||||||
| chr13:28144717
|
T | TC | 155 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.430+5631dupC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144717 | |||||
| chr13:28144718
|
C | CCT | 81 | a0001c0001t0001g0029a0001c0001t0001g0096a0001c0001t0001g0156others(78): Show | 81 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(78): Show |
intron_variant | MODIFIER | c.430+5631_430+5632i others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144718 | ||||||
| chr13:28144718
|
C | CCTT | 6 | a0001c0001t0002g0012a0001c0001t0002g0169a0001c0001t0002g0219others(3): Show | 6 | HG00438.hp2 NA18974.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+5631_430+5632i others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144718 | ||||||
| chr13:28144718
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0004g0057a0001c0001t0006g0137 | 2 | HG01081.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.430+5641_430+5652d others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144718 | |||||
| chr13:28144719
|
T | C | 2 | a0001c0001t0031g0223a0001c0001t0053g0046 | 2 | HG02040.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.430+5632T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144719 | ||||||
| chr13:28144723
|
T | C | 2 | a0001c0001t0010g0124a0001c0001t0028g0125 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.430+5636T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144723 | ||||||
| chr13:28144731
|
T | C | 2 | a0001c0001t0004g0057a0001c0001t0006g0137 | 2 | HG01081.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.430+5644T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144731 | ||||||
| chr13:28144739
|
T | C | 3 | a0001c0001t0026g0239a0001c0001t0031g0223a0001c0007t0021g0151 | 3 | HG00735.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.430+5652T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144739 | ||||||
| chr13:28144839
|
G | GC | 130 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(127): Show | 130 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.430+5753dupC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28144839 | |||||
| chr13:28144841
|
T | C | 1 | a0001c0001t0002g0164 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.430+5754T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144841 | ||||||
| chr13:28144842
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.430+5755C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144842 | ||||||
| chr13:28144856
|
A | G | 2 | a0001c0001t0050g0050a0001c0001t0051g0095 | 2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.430+5769A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144856 | ||||||
| chr13:28144909
|
G | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.430+5822G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28144909 | ||||||
| chr13:28145008
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0050g0050a0001c0001t0051g0095 | 3 | HG02132.hp1 HG02135.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.430+5921G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145008 | ||||||
| chr13:28145009
|
C | T | 2 | a0001c0001t0017g0204a0001c0001t0017g0205 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.430+5922C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145009 | ||||||
| chr13:28145051
|
T | C | 5 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+5964T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145051 | ||||||
| chr13:28145055
|
T | C | 1 | a0001c0001t0023g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.430+5968T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145055 | ||||||
| chr13:28145112
|
G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430+6025G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145112 | ||||||
| chr13:28145234
|
C | T | 1 | a0001c0001t0005g0180 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.430+6147C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145234 | ||||||
| chr13:28145252
|
C | CGT | 13 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(10): Show | 13 | HG01496.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+6176_430+6177d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28145252 | |||||
| chr13:28145252
|
C | CGTGT | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.430+6174_430+6177d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28145252 | |||||
| chr13:28145265
|
A | G | 59 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(56): Show | 59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.430+6178A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145265 | ||||||
| chr13:28145361
|
A | G | 1 | a0001c0001t0011g0242 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.430+6274A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145361 | ||||||
| chr13:28145411
|
G | A | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+6324G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145411 | ||||||
| chr13:28145428
|
A | G | 132 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(129): Show | 132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+6341A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145428 | ||||||
| chr13:28145449
|
T | C | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.430+6362T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145449 | ||||||
| chr13:28145690
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+6603A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145690 | ||||||
| chr13:28145757
|
A | AT | 24 | a0001c0001t0001g0086a0001c0001t0001g0129a0001c0001t0002g0149others(21): Show | 24 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.430+6692dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28145757 | |||||
| chr13:28145757
|
AT | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061others(11): Show | 14 | HG01099.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.430+6692delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28145757 | |||||
| chr13:28145770
|
T | G | 1 | a0001c0001t0003g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.430+6683T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28145770 | ||||||
| chr13:28145908
|
A | AGG | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.430+6822_430+6823d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28145908 | |||||
| chr13:28146088
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+7001C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146088 | ||||||
| chr13:28146157
|
T | C | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+7070T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146157 | ||||||
| chr13:28146300
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.430+7213G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146300 | ||||||
| chr13:28146300
|
G | GTC | 20 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0084others(17): Show | 20 | HG00639.hp2 HG01071.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.430+7238_430+7239d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28146300 | |||||
| chr13:28146300
|
G | GTCTC | 88 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(85): Show | 88 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.430+7236_430+7239d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28146300 | |||||
| chr13:28146300
|
GTC | G | 15 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(12): Show | 15 | HG00735.hp2 HG01099.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.430+7238_430+7239d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28146300 | |||||
| chr13:28146589
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.430+7502A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146589 | ||||||
| chr13:28146650
|
C | T | 4 | a0001c0001t0005g0179a0001c0001t0005g0206a0001c0001t0007g0178others(1): Show | 4 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+7563C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146650 | ||||||
| chr13:28146703
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.430+7616C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146703 | ||||||
| chr13:28146725
|
C | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+7638C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146725 | ||||||
| chr13:28146835
|
C | T | 1 | a0001c0001t0008g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.430+7748C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28146835 | ||||||
| chr13:28147054
|
G | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+7967G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147054 | ||||||
| chr13:28147078
|
C | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+7991C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147078 | ||||||
| chr13:28147274
|
A | G | 250 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(247): Show |
intron_variant | MODIFIER | c.430+8187A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147274 | ||||||
| chr13:28147334
|
G | GT | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+8252dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28147334 | |||||
| chr13:28147370
|
A | C | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430+8283A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147370 | ||||||
| chr13:28147424
|
C | CTT | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+8338_430+8339d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28147424 | |||||
| chr13:28147767
|
A | T | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430+8680A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147767 | ||||||
| chr13:28147888
|
ATTCT | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+8802_430+8805d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28147888 | ||||||
| chr13:28148046
|
G | T | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+8959G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148046 | ||||||
| chr13:28148112
|
T | C | 5 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+9025T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148112 | ||||||
| chr13:28148306
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.430+9219G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148306 | ||||||
| chr13:28148588
|
C | G | 8 | a0001c0001t0001g0056a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG02071.hp2 HG02083.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+9501C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148588 | ||||||
| chr13:28148683
|
C | A | 1 | a0001c0001t0048g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.430+9596C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148683 | ||||||
| chr13:28148857
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+9770A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148857 | ||||||
| chr13:28148903
|
T | A | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+9816T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148903 | ||||||
| chr13:28148923
|
C | T | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+9836C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28148923 | ||||||
| chr13:28149018
|
C | T | 2 | a0001c0001t0026g0239a0001c0007t0021g0151 | 2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.430+9931C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149018 | ||||||
| chr13:28149038
|
C | G | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+9951C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149038 | ||||||
| chr13:28149058
|
T | TA | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+9980dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28149058 | |||||
| chr13:28149192
|
T | C | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+10105T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149192 | ||||||
| chr13:28149311
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18747.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.430+10224C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149311 | ||||||
| chr13:28149371
|
C | T | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+10284C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149371 | ||||||
| chr13:28149377
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0050g0050a0001c0001t0051g0095 | 3 | HG02132.hp1 HG02135.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.430+10290A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149377 | ||||||
| chr13:28149608
|
T | C | 1 | a0001c0001t0003g0168 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.430+10521T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149608 | ||||||
| chr13:28149648
|
GT | G | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.430+10562delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149648 | ||||||
| chr13:28149798
|
G | A | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+10711G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149798 | ||||||
| chr13:28149809
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+10722G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149809 | ||||||
| chr13:28149811
|
C | A | 5 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+10724C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149811 | ||||||
| chr13:28149817
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.430+10730G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28149817 | ||||||
| chr13:28150174
|
A | G | 35 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(32): Show | 35 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.430+11087A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150174 | ||||||
| chr13:28150367
|
T | C | 1 | a0001c0001t0006g0133 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.430+11280T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150367 | ||||||
| chr13:28150391
|
C | T | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+11304C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150391 | ||||||
| chr13:28150466
|
A | C | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+11379A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150466 | ||||||
| chr13:28150499
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026 | 3 | HG02886.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.430+11412C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150499 | ||||||
| chr13:28150612
|
A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.430+11525A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150612 | ||||||
| chr13:28150621
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.430+11534A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150621 | ||||||
| chr13:28150637
|
C | CA | 13 | a0001c0001t0001g0029a0001c0001t0001g0157a0001c0001t0002g0200others(10): Show | 13 | HG01175.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+11567dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28150637 | |||||
| chr13:28150637
|
CA | C | 43 | a0001c0001t0002g0002a0001c0001t0002g0143a0001c0001t0002g0164others(40): Show | 43 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.430+11567delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28150637 | |||||
| chr13:28150709
|
T | G | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.430+11622T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28150709 | ||||||
| chr13:28151021
|
A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.430+11934A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151021 | ||||||
| chr13:28151041
|
C | T | 1 | a0001c0001t0004g0055 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.430+11954C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151041 | ||||||
| chr13:28151325
|
C | G | 3 | a0001c0001t0011g0184a0001c0001t0019g0185a0001c0001t0042g0186 | 3 | HG02109.hp1 HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.430+12238C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151325 | ||||||
| chr13:28151375
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.430+12288C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151375 | ||||||
| chr13:28151489
|
T | A | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.430+12402T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151489 | ||||||
| chr13:28151514
|
CA | C | 23 | a0001c0001t0002g0164a0001c0001t0004g0043a0001c0001t0005g0117others(20): Show | 23 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.430+12439delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28151514 | |||||
| chr13:28151800
|
T | C | 1 | a0001c0001t0004g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.430+12713T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151800 | ||||||
| chr13:28151956
|
C | G | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.430+12869C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28151956 | ||||||
| chr13:28152045
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+12958A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152045 | ||||||
| chr13:28152053
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+12966A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152053 | ||||||
| chr13:28152127
|
A | G | 6 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+13040A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152127 | ||||||
| chr13:28152449
|
T | C | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+13362T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152449 | ||||||
| chr13:28152582
|
G | GA | 7 | a0001c0001t0001g0098a0001c0001t0002g0200a0001c0001t0004g0052others(4): Show | 7 | HG02135.hp1 HG02602.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+13504dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28152582 | |||||
| chr13:28152630
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430+13543A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152630 | ||||||
| chr13:28152692
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+13605G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152692 | ||||||
| chr13:28152694
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+13607T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152694 | ||||||
| chr13:28152919
|
G | C | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.430+13832G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28152919 | ||||||
| chr13:28153232
|
C | CT | 53 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0093others(50): Show | 53 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.430+14167dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28153232 | |||||
| chr13:28153232
|
C | CTT | 53 | a0001c0001t0001g0213a0001c0001t0002g0010a0001c0001t0002g0012others(50): Show | 53 | HG00438.hp2 HG00597.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.430+14166_430+1416 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28153232 | |||||
| chr13:28153232
|
C | CTTT | 20 | a0001c0001t0002g0036a0001c0001t0002g0148a0001c0001t0002g0149others(17): Show | 20 | HG00597.hp1 HG00639.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.430+14165_430+1416 others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28153232 | |||||
| chr13:28153292
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+14205A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153292 | ||||||
| chr13:28153391
|
A | G | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.430+14304A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153391 | ||||||
| chr13:28153522
|
C | A | 2 | a0001c0001t0026g0239a0001c0007t0021g0151 | 2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.430+14435C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153522 | ||||||
| chr13:28153559
|
G | C | 1 | a0001c0004t0004g0064 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.430+14472G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153559 | ||||||
| chr13:28153598
|
T | C | 1 | a0001c0001t0007g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.430+14511T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153598 | ||||||
| chr13:28153651
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430+14564A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153651 | ||||||
| chr13:28153705
|
A | G | 3 | a0001c0001t0008g0245a0001c0001t0008g0246a0001c0001t0008g0247 | 3 | HG01496.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.430+14618A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153705 | ||||||
| chr13:28153731
|
C | G | 6 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+14644C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153731 | ||||||
| chr13:28153889
|
G | A | 72 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(69): Show | 72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.430+14802G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153889 | ||||||
| chr13:28153912
|
T | A | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0014g0111others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+14825T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153912 | ||||||
| chr13:28153942
|
G | C | 1 | a0001c0001t0003g0232 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.430+14855G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153942 | ||||||
| chr13:28153996
|
G | C | 4 | a0001c0001t0013g0015a0001c0001t0013g0127a0001c0001t0013g0128others(1): Show | 4 | HG00099.hp2 HG03225.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+14909G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28153996 | ||||||
| chr13:28154021
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+14934T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154021 | ||||||
| chr13:28154112
|
C | T | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+15025C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154112 | ||||||
| chr13:28154300
|
T | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+15213T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154300 | ||||||
| chr13:28154329
|
C | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+15242C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154329 | ||||||
| chr13:28154342
|
G | A | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.430+15255G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154342 | ||||||
| chr13:28154449
|
C | T | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+15362C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154449 | ||||||
| chr13:28154536
|
C | G | 1 | a0002c0005t0001g0132 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.430+15449C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154536 | ||||||
| chr13:28154564
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.430+15477G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154564 | ||||||
| chr13:28154644
|
T | G | 58 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.430+15557T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154644 | ||||||
| chr13:28154785
|
C | G | 1 | a0001c0001t0009g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.430+15698C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154785 | ||||||
| chr13:28154807
|
GT | G | 36 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0002g0002others(33): Show | 36 | HG00099.hp2 HG01496.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.430+15735delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28154807 | |||||
| chr13:28154807
|
GTT | G | 24 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(21): Show | 24 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.430+15734_430+1573 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28154807 | |||||
| chr13:28154819
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+15732T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154819 | ||||||
| chr13:28154828
|
C | CT | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+15751dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28154828 | |||||
| chr13:28154914
|
G | A | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+15827G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154914 | ||||||
| chr13:28154940
|
C | T | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+15853C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154940 | ||||||
| chr13:28154946
|
G | A | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.430+15859G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28154946 | ||||||
| chr13:28155018
|
C | T | 4 | a0001c0001t0001g0091a0001c0001t0015g0250a0001c0001t0029g0249others(1): Show | 4 | HG03098.hp1 HG03516.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+15931C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155018 | ||||||
| chr13:28155067
|
T | C | 132 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(129): Show | 132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+15980T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155067 | ||||||
| chr13:28155111
|
C | T | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+16024C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155111 | ||||||
| chr13:28155402
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0050g0050a0001c0001t0051g0095 | 3 | HG02132.hp1 HG02135.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.430+16315C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155402 | ||||||
| chr13:28155450
|
T | C | 250 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(247): Show |
intron_variant | MODIFIER | c.430+16363T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155450 | ||||||
| chr13:28155655
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.430+16568G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155655 | ||||||
| chr13:28155658
|
T | G | 1 | a0001c0001t0041g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.430+16571T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155658 | ||||||
| chr13:28155683
|
T | A | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+16596T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155683 | ||||||
| chr13:28155689
|
C | T | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+16602C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155689 | ||||||
| chr13:28155709
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+16622T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155709 | ||||||
| chr13:28155725
|
A | G | 7 | a0001c0001t0002g0143a0001c0001t0002g0145a0001c0001t0002g0146others(4): Show | 7 | HG00438.hp2 NA18941.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+16638A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155725 | ||||||
| chr13:28155729
|
A | T | 1 | a0001c0001t0008g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430+16642A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155729 | ||||||
| chr13:28155734
|
T | C | 1 | a0001c0001t0014g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.430+16647T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155734 | ||||||
| chr13:28155816
|
C | T | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+16729C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155816 | ||||||
| chr13:28155886
|
T | A | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.430+16799T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155886 | ||||||
| chr13:28155886
|
T | G | 74 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(71): Show | 74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.430+16799T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155886 | ||||||
| chr13:28155966
|
C | T | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+16879C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155966 | ||||||
| chr13:28155984
|
A | G | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+16897A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28155984 | ||||||
| chr13:28156155
|
G | T | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.430+17068G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156155 | ||||||
| chr13:28156185
|
AAAG | A | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0032others(14): Show | 17 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.430+17103_430+1710 others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28156185 | |||||
| chr13:28156216
|
G | T | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+17129G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156216 | ||||||
| chr13:28156548
|
T | C | 132 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(129): Show | 132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.430+17461T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156548 | ||||||
| chr13:28156558
|
C | G | 3 | a0001c0001t0002g0002a0001c0001t0003g0001a0001c0001t0003g0003 | 3 | HG02622.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.430+17471C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156558 | ||||||
| chr13:28156831
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-17441A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156831 | ||||||
| chr13:28156869
|
C | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-17403C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156869 | ||||||
| chr13:28156901
|
G | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-17371G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28156901 | ||||||
| chr13:28156992
|
C | CA | 72 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0044others(69): Show | 72 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.431-17253dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28156992 | |||||
| chr13:28156992
|
C | CAA | 36 | a0001c0001t0001g0023a0001c0001t0001g0213a0001c0001t0002g0037others(33): Show | 36 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.431-17254_431-1725 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28156992 | |||||
| chr13:28156992
|
CA | C | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0079others(4): Show | 7 | HG02896.hp1 HG02897.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-17253delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28156992 | |||||
| chr13:28156992
|
CAAAAAAA others(2): Show |
C | 5 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-17261_431-1725 others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28156992 | |||||
| chr13:28157047
|
T | C | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-17225T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28157047 | ||||||
| chr13:28157411
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18747.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.431-16861G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28157411 | ||||||
| chr13:28157436
|
A | G | 1 | a0001c0001t0005g0175 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.431-16836A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28157436 | ||||||
| chr13:28157514
|
C | T | 5 | a0001c0002t0012g0162a0001c0002t0012g0209a0001c0002t0012g0211others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-16758C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28157514 | ||||||
| chr13:28157615
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0003g0001a0001c0001t0003g0003 | 3 | HG02622.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.431-16657G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28157615 | ||||||
| chr13:28158041
|
C | T | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0014g0111others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-16231C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158041 | ||||||
| chr13:28158075
|
T | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-16197T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158075 | ||||||
| chr13:28158164
|
G | A | 72 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(69): Show | 72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.431-16108G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158164 | ||||||
| chr13:28158181
|
A | G | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-16091A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158181 | ||||||
| chr13:28158200
|
A | G | 5 | a0001c0002t0012g0162a0001c0002t0012g0209a0001c0002t0012g0211others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-16072A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158200 | ||||||
| chr13:28158221
|
T | C | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-16051T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158221 | ||||||
| chr13:28158251
|
A | C | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-16021A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158251 | ||||||
| chr13:28158301
|
G | T | 131 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(128): Show | 131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.431-15971G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158301 | ||||||
| chr13:28158326
|
A | G | 1 | a0001c0001t0002g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.431-15946A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158326 | ||||||
| chr13:28158349
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.431-15923G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158349 | ||||||
| chr13:28158594
|
T | G | 1 | a0001c0001t0001g0060 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.431-15678T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158594 | ||||||
| chr13:28158620
|
G | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-15652G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158620 | ||||||
| chr13:28158672
|
A | G | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.431-15600A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158672 | ||||||
| chr13:28158706
|
G | A | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-15566G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158706 | ||||||
| chr13:28158775
|
G | T | 1 | a0001c0001t0006g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.431-15497G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158775 | ||||||
| chr13:28158803
|
G | A | 1 | a0001c0001t0005g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.431-15469G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158803 | ||||||
| chr13:28158835
|
G | A | 22 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(19): Show | 22 | HG00735.hp2 HG01358.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.431-15437G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158835 | ||||||
| chr13:28158901
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.431-15371G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158901 | ||||||
| chr13:28158995
|
G | A | 69 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(66): Show | 69 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.431-15277G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28158995 | ||||||
| chr13:28159107
|
G | A | 131 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(128): Show | 131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.431-15165G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159107 | ||||||
| chr13:28159136
|
T | G | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-15136T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159136 | ||||||
| chr13:28159138
|
A | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-15134A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159138 | ||||||
| chr13:28159224
|
A | G | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-15048A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159224 | ||||||
| chr13:28159404
|
G | C | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-14868G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159404 | ||||||
| chr13:28159405
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-14867T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159405 | ||||||
| chr13:28159477
|
C | T | 2 | a0001c0001t0026g0239a0001c0007t0021g0151 | 2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.431-14795C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159477 | ||||||
| chr13:28159504
|
A | G | 1 | a0001c0001t0046g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.431-14768A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159504 | ||||||
| chr13:28159636
|
T | C | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.431-14636T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159636 | ||||||
| chr13:28159924
|
G | GT | 12 | a0001c0001t0001g0081a0001c0001t0002g0010a0001c0001t0002g0012others(9): Show | 12 | HG02083.hp1 HG02132.hp2 HG03831.hp1 others(9): Show |
intron_variant | MODIFIER | c.431-14336dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28159924 | |||||
| chr13:28159924
|
G | T | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-14348G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28159924 | ||||||
| chr13:28160237
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0049g0154 | 2 | HG01496.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.431-14035C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160237 | ||||||
| chr13:28160247
|
C | A | 2 | a0001c0001t0004g0067a0001c0008t0001g0068 | 2 | HG01358.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.431-14025C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160247 | ||||||
| chr13:28160328
|
T | C | 59 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(56): Show | 59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.431-13944T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160328 | ||||||
| chr13:28160395
|
T | A | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-13877T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160395 | ||||||
| chr13:28160518
|
G | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-13754G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160518 | ||||||
| chr13:28160636
|
A | G | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-13636A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160636 | ||||||
| chr13:28160637
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.431-13635T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160637 | ||||||
| chr13:28160642
|
C | G | 73 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(70): Show | 73 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.431-13630C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160642 | ||||||
| chr13:28160752
|
G | C | 3 | a0001c0001t0002g0201a0001c0001t0002g0236a0001c0001t0003g0235 | 3 | NA19062.hp2 NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.431-13520G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160752 | ||||||
| chr13:28160795
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.431-13477T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160795 | ||||||
| chr13:28160845
|
G | A | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-13427G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160845 | ||||||
| chr13:28160847
|
T | A | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.431-13425T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160847 | ||||||
| chr13:28160936
|
G | T | 1 | a0001c0001t0016g0196 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.431-13336G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28160936 | ||||||
| chr13:28161662
|
T | C | 3 | a0001c0001t0001g0103a0001c0001t0004g0092a0001c0001t0004g0104 | 3 | HG01346.hp1 HG01433.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.431-12610T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28161662 | ||||||
| chr13:28161847
|
A | G | 1 | a0001c0002t0012g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.431-12425A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28161847 | ||||||
| chr13:28161921
|
G | A | 1 | a0001c0001t0006g0133 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.431-12351G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28161921 | ||||||
| chr13:28161924
|
A | G | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.431-12348A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28161924 | ||||||
| chr13:28162022
|
A | G | 3 | a0001c0001t0008g0245a0001c0001t0008g0246a0001c0001t0008g0247 | 3 | HG01496.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.431-12250A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162022 | ||||||
| chr13:28162030
|
T | C | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.431-12242T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162030 | ||||||
| chr13:28162098
|
A | G | 4 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0008others(1): Show | 4 | HG02083.hp1 NA18979.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-12174A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162098 | ||||||
| chr13:28162307
|
G | A | 56 | a0001c0001t0001g0213a0001c0001t0002g0010a0001c0001t0002g0012others(53): Show | 56 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.431-11965G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162307 | ||||||
| chr13:28162333
|
C | T | 1 | a0001c0001t0010g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.431-11939C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162333 | ||||||
| chr13:28162410
|
T | C | 58 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.431-11862T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162410 | ||||||
| chr13:28162489
|
A | C | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-11783A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162489 | ||||||
| chr13:28162555
|
G | A | 1 | a0001c0003t0014g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.431-11717G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162555 | ||||||
| chr13:28162624
|
G | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-11648G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162624 | ||||||
| chr13:28162644
|
C | T | 2 | a0001c0001t0002g0197a0001c0001t0002g0217 | 2 | NA19002.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.431-11628C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162644 | ||||||
| chr13:28162646
|
T | TAA | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.431-11615_431-1161 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28162646 | |||||
| chr13:28162732
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.431-11540A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162732 | ||||||
| chr13:28162833
|
C | A | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-11439C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162833 | ||||||
| chr13:28162949
|
T | C | 7 | a0001c0001t0002g0195a0001c0001t0002g0234a0001c0001t0003g0216others(4): Show | 7 | HG01261.hp2 NA18948.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-11323T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28162949 | ||||||
| chr13:28163132
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.431-11140T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163132 | ||||||
| chr13:28163212
|
A | C | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.431-11060A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163212 | ||||||
| chr13:28163311
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-10961A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163311 | ||||||
| chr13:28163502
|
A | G | 56 | a0001c0001t0001g0213a0001c0001t0002g0010a0001c0001t0002g0012others(53): Show | 56 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.431-10770A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163502 | ||||||
| chr13:28163652
|
T | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-10620T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163652 | ||||||
| chr13:28163715
|
A | G | 5 | a0001c0001t0001g0138a0001c0001t0001g0156a0001c0001t0004g0153others(2): Show | 5 | HG00438.hp1 NA18941.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-10557A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163715 | ||||||
| chr13:28163717
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-10555A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163717 | ||||||
| chr13:28163812
|
G | A | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-10460G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163812 | ||||||
| chr13:28163824
|
A | C | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-10448A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163824 | ||||||
| chr13:28163861
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.431-10411T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28163861 | ||||||
| chr13:28164052
|
C | T | 2 | a0001c0001t0011g0184a0001c0001t0019g0185 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.431-10220C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164052 | ||||||
| chr13:28164468
|
A | G | 2 | a0001c0001t0026g0239a0001c0007t0021g0151 | 2 | HG00735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.431-9804A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164468 | ||||||
| chr13:28164507
|
T | C | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-9765T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164507 | ||||||
| chr13:28164528
|
T | A | 2 | a0001c0001t0002g0233a0001c0001t0002g0240 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.431-9744T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164528 | ||||||
| chr13:28164794
|
A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-9478A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164794 | ||||||
| chr13:28164918
|
A | AT | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-9345dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28164918 | |||||
| chr13:28164963
|
A | G | 75 | a0001c0001t0001g0114a0001c0001t0001g0213a0001c0001t0002g0002others(72): Show | 75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.431-9309A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28164963 | ||||||
| chr13:28165097
|
G | A | 5 | a0001c0001t0008g0007a0001c0001t0008g0245a0001c0001t0008g0246others(2): Show | 5 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-9175G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165097 | ||||||
| chr13:28165243
|
A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-9029A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165243 | ||||||
| chr13:28165283
|
C | CT | 79 | a0001c0001t0001g0077a0001c0001t0001g0094a0001c0001t0001g0213others(76): Show | 79 | HG00438.hp2 HG00597.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.431-8972dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28165283 | |||||
| chr13:28165283
|
C | CTT | 20 | a0001c0001t0003g0224a0001c0001t0003g0232a0001c0001t0005g0117others(17): Show | 20 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.431-8973_431-8972d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28165283 | |||||
| chr13:28165283
|
C | CTTT | 7 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(4): Show | 7 | HG00639.hp2 HG01099.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-8974_431-8972d others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28165283 | |||||
| chr13:28165313
|
G | A | 1 | a0001c0001t0004g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.431-8959G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165313 | ||||||
| chr13:28165324
|
T | C | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-8948T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165324 | ||||||
| chr13:28165753
|
C | A | 6 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-8519C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165753 | ||||||
| chr13:28165856
|
T | G | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-8416T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28165856 | ||||||
| chr13:28166206
|
A | G | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-8066A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166206 | ||||||
| chr13:28166551
|
T | C | 11 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(8): Show | 11 | HG01496.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.431-7721T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166551 | ||||||
| chr13:28166609
|
A | G | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-7663A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166609 | ||||||
| chr13:28166643
|
C | T | 1 | a0001c0001t0004g0153 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.431-7629C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166643 | ||||||
| chr13:28166689
|
G | A | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-7583G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166689 | ||||||
| chr13:28166790
|
G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-7482G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166790 | ||||||
| chr13:28166964
|
C | T | 1 | a0001c0001t0009g0198 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.431-7308C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28166964 | ||||||
| chr13:28167082
|
A | AT | 87 | a0001c0001t0001g0084a0001c0001t0001g0094a0001c0001t0001g0114others(84): Show | 87 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(84): Show |
intron_variant | MODIFIER | c.431-7168dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28167082 | |||||
| chr13:28167082
|
A | T | 31 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(28): Show | 31 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.431-7190A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167082 | ||||||
| chr13:28167093
|
T | A | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-7179T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167093 | ||||||
| chr13:28167233
|
C | G | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.431-7039C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167233 | ||||||
| chr13:28167326
|
A | T | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-6946A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167326 | ||||||
| chr13:28167347
|
A | T | 15 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(12): Show | 15 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.431-6925A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167347 | ||||||
| chr13:28167363
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.431-6909G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167363 | ||||||
| chr13:28167436
|
T | C | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-6836T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167436 | ||||||
| chr13:28167452
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.431-6820C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167452 | ||||||
| chr13:28167456
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-6816C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167456 | ||||||
| chr13:28167621
|
G | A | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-6651G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167621 | ||||||
| chr13:28167673
|
C | CA | 52 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0044others(49): Show | 52 | HG00735.hp1 HG00735.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.431-6578dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28167673 | |||||
| chr13:28167677
|
A | C | 2 | a0001c0001t0017g0204a0001c0001t0017g0205 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.431-6595A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167677 | ||||||
| chr13:28167681
|
A | C | 2 | a0001c0001t0017g0204a0001c0001t0017g0205 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.431-6591A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167681 | ||||||
| chr13:28167808
|
C | T | 1 | a0001c0001t0006g0137 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.431-6464C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167808 | ||||||
| chr13:28167908
|
C | G | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.431-6364C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167908 | ||||||
| chr13:28167924
|
A | G | 1 | a0001c0001t0003g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.431-6348A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28167924 | ||||||
| chr13:28168056
|
C | T | 1 | a0001c0003t0014g0078 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.431-6216C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168056 | ||||||
| chr13:28168176
|
C | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-6096C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168176 | ||||||
| chr13:28168335
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.431-5937A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168335 | ||||||
| chr13:28168356
|
G | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-5916G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168356 | ||||||
| chr13:28168402
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.431-5870A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168402 | ||||||
| chr13:28168402
|
A | T | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.431-5870A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168402 | ||||||
| chr13:28168438
|
C | G | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.431-5834C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168438 | ||||||
| chr13:28168501
|
T | C | 2 | a0001c0001t0006g0016a0001c0001t0006g0017 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.431-5771T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168501 | ||||||
| chr13:28168637
|
T | G | 1 | a0001c0001t0009g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.431-5635T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168637 | ||||||
| chr13:28168643
|
C | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-5629C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168643 | ||||||
| chr13:28168751
|
G | A | 3 | a0001c0003t0001g0136a0001c0003t0004g0135a0001c0003t0014g0078 | 3 | HG02922.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.431-5521G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168751 | ||||||
| chr13:28168773
|
C | T | 22 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(19): Show | 22 | HG00735.hp2 HG01358.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.431-5499C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168773 | ||||||
| chr13:28168863
|
A | G | 1 | a0001c0001t0042g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.431-5409A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168863 | ||||||
| chr13:28168942
|
C | T | 1 | a0001c0001t0009g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.431-5330C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168942 | ||||||
| chr13:28168994
|
C | T | 1 | a0001c0001t0008g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.431-5278C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28168994 | ||||||
| chr13:28169010
|
C | G | 1 | a0001c0001t0002g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.431-5262C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169010 | ||||||
| chr13:28169015
|
C | CA | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-5244dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169015 | |||||
| chr13:28169051
|
A | G | 7 | a0001c0001t0002g0143a0001c0001t0002g0145a0001c0001t0002g0146others(4): Show | 7 | HG00438.hp2 NA18941.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-5221A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169051 | ||||||
| chr13:28169222
|
C | CT | 18 | a0001c0001t0001g0034a0001c0001t0001g0054a0001c0001t0001g0061others(15): Show | 18 | HG00438.hp1 HG01109.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.431-5026dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169222 | |||||
| chr13:28169222
|
C | CTT | 5 | a0001c0001t0006g0053a0001c0001t0010g0152a0001c0001t0025g0203others(2): Show | 5 | HG01358.hp2 HG02258.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-5027_431-5026d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169222 | |||||
| chr13:28169222
|
CT | C | 39 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0060others(36): Show | 39 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.431-5026delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169222 | |||||
| chr13:28169222
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0003g0003a0001c0001t0003g0231a0001c0001t0009g0194 | 3 | HG02647.hp1 NA18943.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.431-5035_431-5026d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169222 | |||||
| chr13:28169222
|
CTTTTTTT others(4): Show |
C | 67 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(64): Show | 67 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.431-5036_431-5026d others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28169222 | |||||
| chr13:28169373
|
G | C | 1 | a0001c0001t0048g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.431-4899G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169373 | ||||||
| chr13:28169384
|
C | G | 1 | a0001c0001t0056g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.431-4888C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169384 | ||||||
| chr13:28169398
|
G | T | 58 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.431-4874G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169398 | ||||||
| chr13:28169527
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.431-4745G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169527 | ||||||
| chr13:28169550
|
C | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0025others(1): Show | 4 | HG01099.hp2 HG01167.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-4722C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169550 | ||||||
| chr13:28169658
|
C | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-4614C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169658 | ||||||
| chr13:28169724
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.431-4548A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169724 | ||||||
| chr13:28169770
|
C | T | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.431-4502C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169770 | ||||||
| chr13:28169786
|
C | T | 1 | a0001c0001t0007g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.431-4486C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28169786 | ||||||
| chr13:28170228
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.431-4044A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28170228 | ||||||
| chr13:28170280
|
A | G | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-3992A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28170280 | ||||||
| chr13:28170347
|
A | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-3925A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28170347 | ||||||
| chr13:28170451
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-3821T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28170451 | ||||||
| chr13:28170472
|
T | A | 36 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(33): Show | 36 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.431-3800T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28170472 | ||||||
| chr13:28170767
|
CATAAG | C | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-3500_431-3496d others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28170767 | |||||
| chr13:28171043
|
G | A | 6 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-3229G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171043 | ||||||
| chr13:28171275
|
T | C | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.431-2997T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171275 | ||||||
| chr13:28171275
|
T | TTCTC | 134 | a0001c0001t0001g0096a0001c0001t0001g0157a0001c0001t0001g0213others(131): Show | 134 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.431-2994_431-2993i others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr13 | 28171275 | |||||
| chr13:28171476
|
G | A | 1 | a0001c0001t0007g0237 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.431-2796G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171476 | ||||||
| chr13:28171535
|
G | A | 1 | a0001c0001t0006g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.431-2737G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171535 | ||||||
| chr13:28171645
|
A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-2627A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171645 | ||||||
| chr13:28171684
|
C | A | 1 | a0001c0001t0013g0015 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.431-2588C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28171684 | ||||||
| chr13:28172019
|
T | C | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-2253T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172019 | ||||||
| chr13:28172046
|
A | G | 1 | a0001c0001t0011g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.431-2226A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172046 | ||||||
| chr13:28172289
|
T | A | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1983T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172289 | ||||||
| chr13:28172480
|
T | G | 1 | a0001c0001t0024g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431-1792T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172480 | ||||||
| chr13:28172492
|
A | G | 1 | a0001c0001t0024g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431-1780A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172492 | ||||||
| chr13:28172648
|
C | T | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-1624C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172648 | ||||||
| chr13:28172649
|
T | C | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.431-1623T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172649 | ||||||
| chr13:28172774
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.431-1498A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172774 | ||||||
| chr13:28172873
|
A | G | 1 | a0001c0001t0006g0013 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.431-1399A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172873 | ||||||
| chr13:28172955
|
C | A | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1317C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172955 | ||||||
| chr13:28172985
|
C | G | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.431-1287C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28172985 | ||||||
| chr13:28173232
|
C | G | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-1040C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173232 | ||||||
| chr13:28173269
|
G | A | 251 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(248): Show |
intron_variant | MODIFIER | c.431-1003G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173269 | ||||||
| chr13:28173533
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-739A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173533 | ||||||
| chr13:28173682
|
A | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-590A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173682 | ||||||
| chr13:28173752
|
A | G | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.431-520A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173752 | ||||||
| chr13:28173920
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431-352C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173920 | ||||||
| chr13:28173963
|
T | G | 1 | a0001c0001t0053g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.431-309T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28173963 | ||||||
| chr13:28174070
|
G | A | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.431-202G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28174070 | ||||||
| chr13:28174132
|
A | G | 2 | a0001c0001t0011g0184a0001c0001t0019g0185 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.431-140A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 1/18 | chr13 | 28174132 | ||||||
| chr13:28174918
|
G | C | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.552+525G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28174918 | ||||||
| chr13:28174944
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.552+551T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28174944 | ||||||
| chr13:28175161
|
A | G | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.552+768A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175161 | ||||||
| chr13:28175178
|
A | C | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.552+785A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175178 | ||||||
| chr13:28175207
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.552+814G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175207 | ||||||
| chr13:28175351
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.552+958A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175351 | ||||||
| chr13:28175393
|
G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.552+1000G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175393 | ||||||
| chr13:28175594
|
T | C | 59 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(56): Show | 59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.553-899T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175594 | ||||||
| chr13:28175657
|
G | A | 2 | a0001c0001t0003g0216a0001c0001t0003g0218 | 2 | NA19082.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.553-836G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175657 | ||||||
| chr13:28175877
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.553-616C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175877 | ||||||
| chr13:28175911
|
G | T | 1 | a0001c0001t0003g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.553-582G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175911 | ||||||
| chr13:28175992
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.553-501C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28175992 | ||||||
| chr13:28176048
|
G | A | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.553-445G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28176048 | ||||||
| chr13:28176406
|
G | A | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.553-87G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 2/18 | chr13 | 28176406 | ||||||
| chr13:28176800
|
A | C | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.619+241A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28176800 | ||||||
| chr13:28176847
|
T | TA | 7 | a0001c0001t0004g0065a0001c0001t0017g0204a0001c0001t0017g0205others(4): Show | 7 | HG01261.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.619+299dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 28176847 | |||||
| chr13:28176854
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.619+295A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28176854 | ||||||
| chr13:28177013
|
A | C | 1 | a0001c0001t0004g0099 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.619+454A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177013 | ||||||
| chr13:28177226
|
AT | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.620-636delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr13 | 28177226 | |||||
| chr13:28177249
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.620-616T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177249 | ||||||
| chr13:28177468
|
A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.620-397A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177468 | ||||||
| chr13:28177542
|
T | C | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.620-323T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177542 | ||||||
| chr13:28177705
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.620-160T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177705 | ||||||
| chr13:28177770
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.620-95A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177770 | ||||||
| chr13:28177800
|
A | G | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.620-65A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177800 | ||||||
| chr13:28177817
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.620-48G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177817 | ||||||
| chr13:28177827
|
A | G | 1 | a0001c0001t0003g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.620-38A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 3/18 | chr13 | 28177827 | ||||||
| chr13:28177978
|
A | C | 70 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(67): Show | 70 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.690+43A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28177978 | ||||||
| chr13:28178238
|
T | C | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.690+303T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28178238 | ||||||
| chr13:28178240
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.690+305T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28178240 | ||||||
| chr13:28178257
|
G | A | 132 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(129): Show | 132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.690+322G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28178257 | ||||||
| chr13:28178903
|
T | C | 1 | a0001c0001t0003g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.690+968T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28178903 | ||||||
| chr13:28178999
|
AC | A | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.690+1065delC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28178999 | ||||||
| chr13:28179006
|
T | C | 2 | a0001c0001t0002g0227a0001c0001t0022g0228 | 2 | HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.690+1071T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179006 | ||||||
| chr13:28179286
|
T | C | 1 | a0001c0001t0007g0183 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.690+1351T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179286 | ||||||
| chr13:28179472
|
T | C | 1 | a0001c0001t0008g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.690+1537T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179472 | ||||||
| chr13:28179485
|
C | T | 1 | a0001c0001t0008g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.690+1550C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179485 | ||||||
| chr13:28179508
|
A | G | 73 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(70): Show | 73 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.690+1573A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179508 | ||||||
| chr13:28179528
|
A | G | 1 | a0001c0001t0004g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.690+1593A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179528 | ||||||
| chr13:28179594
|
C | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+1659C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179594 | ||||||
| chr13:28179602
|
G | A | 8 | a0001c0001t0002g0195a0001c0001t0002g0221a0001c0001t0002g0234others(5): Show | 8 | HG00597.hp1 HG01261.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+1667G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179602 | ||||||
| chr13:28179633
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.690+1698G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179633 | ||||||
| chr13:28179670
|
C | T | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+1735C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179670 | ||||||
| chr13:28179707
|
C | CA | 43 | a0001c0001t0001g0020a0001c0001t0002g0148a0001c0001t0004g0052others(40): Show | 43 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.690+1787dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28179707 | |||||
| chr13:28179751
|
C | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+1816C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179751 | ||||||
| chr13:28179948
|
A | G | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.690+2013A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28179948 | ||||||
| chr13:28180461
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+2526G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28180461 | ||||||
| chr13:28180743
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+2808T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28180743 | ||||||
| chr13:28180821
|
A | G | 4 | a0001c0001t0011g0187a0001c0001t0011g0242a0001c0001t0019g0238others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+2886A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28180821 | ||||||
| chr13:28181038
|
A | T | 1 | a0001c0001t0002g0170 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.690+3103A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181038 | ||||||
| chr13:28181067
|
A | C | 6 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+3132A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181067 | ||||||
| chr13:28181236
|
C | G | 62 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(59): Show | 62 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.690+3301C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181236 | ||||||
| chr13:28181400
|
C | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+3465C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181400 | ||||||
| chr13:28181460
|
C | G | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+3525C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181460 | ||||||
| chr13:28181504
|
C | CA | 31 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0025others(28): Show | 31 | HG00438.hp2 HG01099.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.690+3593dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28181504 | |||||
| chr13:28181504
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0100 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.690+3584_690+3593d others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28181504 | |||||
| chr13:28181721
|
A | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+3786A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28181721 | ||||||
| chr13:28182311
|
A | G | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+4376A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28182311 | ||||||
| chr13:28182418
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.690+4483G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28182418 | ||||||
| chr13:28182920
|
C | T | 4 | a0001c0001t0025g0203a0001c0001t0026g0239a0001c0001t0038g0243others(1): Show | 4 | HG00735.hp2 HG01358.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+4985C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28182920 | ||||||
| chr13:28182921
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.690+4986A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28182921 | ||||||
| chr13:28182940
|
C | T | 132 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(129): Show | 132 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.690+5005C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28182940 | ||||||
| chr13:28183727
|
A | G | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+5792A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28183727 | ||||||
| chr13:28183900
|
G | A | 131 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(128): Show | 131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.690+5965G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28183900 | ||||||
| chr13:28183976
|
ACT | A | 5 | a0001c0001t0008g0007a0001c0001t0008g0245a0001c0001t0008g0246others(2): Show | 5 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.690+6044_690+6045d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28183976 | |||||
| chr13:28184013
|
A | G | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+6078A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184013 | ||||||
| chr13:28184015
|
G | A | 17 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(14): Show | 17 | HG00735.hp2 HG01358.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.690+6080G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184015 | ||||||
| chr13:28184267
|
ATAAT | A | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.690+6335_690+6338d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28184267 | |||||
| chr13:28184339
|
GA | G | 12 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.690+6405delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184339 | ||||||
| chr13:28184456
|
G | A | 14 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(11): Show | 14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.690+6521G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184456 | ||||||
| chr13:28184466
|
C | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+6531C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184466 | ||||||
| chr13:28184501
|
G | A | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+6566G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184501 | ||||||
| chr13:28184828
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.690+6893A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184828 | ||||||
| chr13:28184833
|
T | G | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.690+6898T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184833 | ||||||
| chr13:28184900
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.690+6965C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28184900 | ||||||
| chr13:28185055
|
G | C | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+7120G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185055 | ||||||
| chr13:28185095
|
T | G | 2 | a0001c0001t0006g0030a0001c0001t0045g0102 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.690+7160T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185095 | ||||||
| chr13:28185100
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+7165A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185100 | ||||||
| chr13:28185151
|
C | T | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.690+7216C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185151 | ||||||
| chr13:28185167
|
A | G | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+7232A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185167 | ||||||
| chr13:28185361
|
G | A | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.690+7426G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185361 | ||||||
| chr13:28185493
|
C | T | 1 | a0001c0001t0009g0220 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.690+7558C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185493 | ||||||
| chr13:28185715
|
G | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.690+7780G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185715 | ||||||
| chr13:28185747
|
A | G | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.690+7812A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185747 | ||||||
| chr13:28185765
|
C | T | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.690+7830C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185765 | ||||||
| chr13:28185846
|
G | A | 2 | a0001c0001t0016g0040a0001c0001t0036g0041 | 2 | NA18956.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.690+7911G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28185846 | ||||||
| chr13:28186176
|
A | AATACAAA others(324): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA18747.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.690+8258_690+8259i others(333): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28186176 | |||||
| chr13:28186548
|
AGTTT | A | 88 | a0001c0001t0001g0083a0001c0001t0001g0130a0001c0001t0001g0131others(85): Show | 88 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.690+8618_690+8621d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28186548 | |||||
| chr13:28186719
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+8784A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28186719 | ||||||
| chr13:28186803
|
A | G | 144 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(141): Show | 144 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.690+8868A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28186803 | ||||||
| chr13:28186903
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.690+8968A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28186903 | ||||||
| chr13:28186911
|
C | G | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.690+8976C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28186911 | ||||||
| chr13:28187270
|
C | T | 1 | a0001c0001t0005g0179 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.690+9335C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187270 | ||||||
| chr13:28187357
|
A | G | 1 | a0001c0001t0045g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.690+9422A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187357 | ||||||
| chr13:28187506
|
C | A | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+9571C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187506 | ||||||
| chr13:28187655
|
C | T | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.691-9530C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187655 | ||||||
| chr13:28187683
|
A | G | 10 | a0001c0001t0002g0191a0001c0001t0002g0200a0001c0001t0002g0202others(7): Show | 10 | HG02080.hp1 HG02135.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.691-9502A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187683 | ||||||
| chr13:28187726
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0074a0001c0001t0001g0101others(1): Show | 4 | HG02523.hp2 NA18747.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-9459C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28187726 | ||||||
| chr13:28188027
|
CTA | C | 3 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0032g0225 | 3 | HG02258.hp1 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.691-9156_691-9155d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28188027 | |||||
| chr13:28188035
|
T | G | 9 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.691-9150T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188035 | ||||||
| chr13:28188114
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.691-9071C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188114 | ||||||
| chr13:28188196
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.691-8989T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188196 | ||||||
| chr13:28188221
|
A | G | 1 | a0001c0001t0007g0177 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.691-8964A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188221 | ||||||
| chr13:28188250
|
A | AT | 145 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(142): Show | 145 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.691-8927dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28188250 | |||||
| chr13:28188285
|
T | A | 1 | a0001c0001t0003g0232 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.691-8900T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188285 | ||||||
| chr13:28188286
|
T | G | 1 | a0001c0001t0003g0232 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.691-8899T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188286 | ||||||
| chr13:28188468
|
G | C | 1 | a0001c0001t0002g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.691-8717G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188468 | ||||||
| chr13:28188602
|
AAAAG | A | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.691-8579_691-8576d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28188602 | |||||
| chr13:28188844
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0079 | 2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.691-8341A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188844 | ||||||
| chr13:28188908
|
T | G | 2 | a0001c0001t0001g0155a0001c0001t0049g0154 | 2 | HG01496.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.691-8277T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28188908 | ||||||
| chr13:28189159
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.691-8026A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189159 | ||||||
| chr13:28189374
|
G | C | 3 | a0001c0001t0001g0058a0001c0001t0050g0050a0001c0001t0051g0095 | 3 | HG02132.hp1 HG02135.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.691-7811G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189374 | ||||||
| chr13:28189464
|
C | T | 3 | a0001c0001t0005g0117a0001c0001t0005g0180a0001c0001t0031g0223 | 3 | HG02056.hp2 HG03098.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.691-7721C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189464 | ||||||
| chr13:28189509
|
C | G | 3 | a0001c0001t0002g0002a0001c0001t0003g0001a0001c0001t0003g0003 | 3 | HG02622.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.691-7676C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189509 | ||||||
| chr13:28189533
|
A | G | 1 | a0001c0001t0029g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.691-7652A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189533 | ||||||
| chr13:28189534
|
C | CA | 13 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(10): Show | 13 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.691-7647dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28189534 | |||||
| chr13:28189537
|
A | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.691-7648A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189537 | ||||||
| chr13:28189538
|
AC | A | 86 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(83): Show | 86 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.691-7646delC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189538 | ||||||
| chr13:28189539
|
C | A | 63 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.691-7646C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189539 | ||||||
| chr13:28189598
|
C | A | 1 | a0001c0001t0009g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.691-7587C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189598 | ||||||
| chr13:28189732
|
A | G | 1 | a0001c0001t0009g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.691-7453A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189732 | ||||||
| chr13:28189900
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0004g0090 | 2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.691-7285T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28189900 | ||||||
| chr13:28190033
|
C | T | 144 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(141): Show | 144 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.691-7152C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190033 | ||||||
| chr13:28190089
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.691-7096G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190089 | ||||||
| chr13:28190188
|
G | A | 1 | a0001c0001t0002g0167 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.691-6997G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190188 | ||||||
| chr13:28190460
|
TG | T | 5 | a0001c0002t0012g0162a0001c0002t0012g0209a0001c0002t0012g0211others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-6724delG | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190460 | ||||||
| chr13:28190629
|
C | T | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.691-6556C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190629 | ||||||
| chr13:28190793
|
T | G | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.691-6392T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190793 | ||||||
| chr13:28190864
|
C | G | 2 | a0001c0001t0023g0171a0001c0001t0024g0226 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.691-6321C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190864 | ||||||
| chr13:28190886
|
G | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-6299G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28190886 | ||||||
| chr13:28191062
|
A | T | 1 | a0001c0001t0019g0238 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.691-6123A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191062 | ||||||
| chr13:28191181
|
T | C | 57 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(54): Show | 57 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.691-6004T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191181 | ||||||
| chr13:28191272
|
C | T | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.691-5913C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191272 | ||||||
| chr13:28191391
|
G | T | 2 | a0001c0001t0002g0227a0001c0001t0022g0228 | 2 | HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.691-5794G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191391 | ||||||
| chr13:28191477
|
G | A | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.691-5708G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191477 | ||||||
| chr13:28191537
|
C | T | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-5648C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191537 | ||||||
| chr13:28191803
|
T | G | 1 | a0001c0001t0002g0197 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.691-5382T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191803 | ||||||
| chr13:28191818
|
C | T | 2 | a0001c0003t0001g0136a0001c0003t0004g0135 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.691-5367C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191818 | ||||||
| chr13:28191991
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.691-5194C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28191991 | ||||||
| chr13:28192016
|
C | T | 3 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0147 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.691-5169C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28192016 | ||||||
| chr13:28192048
|
C | CT | 9 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0134others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-5118dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28192048 | |||||
| chr13:28192048
|
CT | C | 115 | a0001c0001t0001g0061a0001c0001t0001g0107a0001c0001t0001g0130others(112): Show | 115 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.691-5118delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28192048 | |||||
| chr13:28192048
|
CTT | C | 11 | a0001c0001t0002g0143a0001c0001t0002g0145a0001c0001t0002g0146others(8): Show | 11 | HG02109.hp1 HG02572.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.691-5119_691-5118d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28192048 | |||||
| chr13:28192127
|
C | T | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.691-5058C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28192127 | ||||||
| chr13:28192357
|
C | T | 5 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-4828C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28192357 | ||||||
| chr13:28192607
|
C | G | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.691-4578C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28192607 | ||||||
| chr13:28192930
|
T | C | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.691-4255T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28192930 | ||||||
| chr13:28193205
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-3980A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193205 | ||||||
| chr13:28193254
|
A | T | 2 | a0001c0001t0017g0204a0001c0001t0017g0205 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.691-3931A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193254 | ||||||
| chr13:28193284
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.691-3901A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193284 | ||||||
| chr13:28193496
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG02055.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-3689C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193496 | ||||||
| chr13:28193604
|
G | C | 88 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(85): Show | 88 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.691-3581G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193604 | ||||||
| chr13:28193614
|
A | C | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.691-3571A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193614 | ||||||
| chr13:28193705
|
T | A | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.691-3480T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193705 | ||||||
| chr13:28193736
|
T | TA | 180 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(177): Show | 180 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.691-3429dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28193736 | |||||
| chr13:28193736
|
T | TAA | 34 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0089others(31): Show | 34 | HG01175.hp2 HG01261.hp1 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.691-3430_691-3429d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28193736 | |||||
| chr13:28193756
|
A | AAC | 12 | a0001c0001t0005g0179a0001c0001t0005g0188a0001c0001t0011g0184others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.691-3429_691-3428i others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193756 | ||||||
| chr13:28193756
|
A | AC | 20 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(17): Show | 20 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.691-3426dupC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28193756 | |||||
| chr13:28193791
|
CT | C | 5 | a0001c0002t0012g0162a0001c0002t0012g0209a0001c0002t0012g0211others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-3386delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28193791 | |||||
| chr13:28193807
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.691-3378G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193807 | ||||||
| chr13:28193819
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.691-3366A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193819 | ||||||
| chr13:28193847
|
G | T | 6 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-3338G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193847 | ||||||
| chr13:28193865
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.691-3320G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193865 | ||||||
| chr13:28193866
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.691-3319T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193866 | ||||||
| chr13:28193885
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.691-3300G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193885 | ||||||
| chr13:28193913
|
T | C | 1 | a0001c0001t0003g0009 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.691-3272T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193913 | ||||||
| chr13:28193914
|
T | C | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.691-3271T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193914 | ||||||
| chr13:28193917
|
G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.691-3268G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28193917 | ||||||
| chr13:28194154
|
AAAAT | A | 33 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0036others(30): Show | 33 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.691-3027_691-3024d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194154 | |||||
| chr13:28194259
|
A | T | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-2926A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194259 | ||||||
| chr13:28194277
|
G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.691-2908G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194277 | ||||||
| chr13:28194408
|
A | G | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-2777A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194408 | ||||||
| chr13:28194437
|
CATATATA others(11): Show |
C | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.691-2739_691-2722d others(20): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194437 | |||||
| chr13:28194450
|
G | GTA | 14 | a0001c0001t0002g0227a0001c0001t0005g0117a0001c0001t0005g0176others(11): Show | 14 | HG00099.hp1 HG00597.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.691-2719_691-2718d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194450 | |||||
| chr13:28194450
|
G | GTATA | 6 | a0001c0001t0002g0036a0001c0001t0002g0166a0001c0001t0002g0167others(3): Show | 6 | HG02132.hp2 HG02165.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-2721_691-2718d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194450 | |||||
| chr13:28194452
|
A | G | 3 | a0001c0001t0003g0001a0001c0001t0003g0165a0001c0001t0025g0203 | 3 | HG01358.hp2 HG02155.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.691-2733A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194452 | ||||||
| chr13:28194464
|
A | AT | 7 | a0001c0001t0002g0002a0001c0001t0002g0233a0001c0001t0002g0240others(4): Show | 7 | HG01167.hp2 HG01891.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-2720dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194464 | |||||
| chr13:28194464
|
A | ATT | 4 | a0001c0001t0003g0003a0001c0001t0008g0007a0001c0001t0008g0248others(1): Show | 4 | HG02976.hp2 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-2720_691-2719i others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194464 | |||||
| chr13:28194464
|
A | T | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.691-2721A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194464 | ||||||
| chr13:28194466
|
A | AT | 8 | a0001c0001t0006g0013a0001c0001t0006g0016a0001c0001t0006g0017others(5): Show | 8 | HG01069.hp1 HG01081.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.691-2700dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194466 | |||||
| chr13:28194466
|
A | ATATATAT others(8): Show |
4 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0126others(1): Show | 4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-2718_691-2717i others(17): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194466 | |||||
| chr13:28194466
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0010g0124a0001c0001t0028g0125 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.691-2718_691-2717i others(17): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194466 | |||||
| chr13:28194466
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0033g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.691-2718_691-2717i others(15): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194466 | |||||
| chr13:28194466
|
A | ATT | 7 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(4): Show | 7 | HG01496.hp1 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-2701_691-2700d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194466 | |||||
| chr13:28194466
|
A | T | 14 | a0001c0001t0002g0002a0001c0001t0002g0233a0001c0001t0002g0240others(11): Show | 14 | HG01167.hp2 HG01891.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.691-2719A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194466 | ||||||
| chr13:28194467
|
T | TA | 18 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0100others(15): Show | 18 | HG01071.hp2 HG01099.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.691-2718_691-2717i others(3): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194467 | ||||||
| chr13:28194467
|
T | TATA | 59 | a0001c0001t0001g0213a0001c0001t0002g0012a0001c0001t0002g0038others(56): Show | 59 | HG00438.hp2 HG00639.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.691-2718_691-2717i others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194467 | ||||||
| chr13:28194467
|
T | TATATA | 11 | a0001c0001t0002g0010a0001c0001t0002g0037a0001c0001t0002g0221others(8): Show | 11 | HG00597.hp1 HG00639.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.691-2718_691-2717i others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194467 | ||||||
| chr13:28194468
|
T | A | 114 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.691-2717T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194468 | ||||||
| chr13:28194469
|
T | A | 73 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0100others(70): Show | 73 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.691-2716T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194469 | ||||||
| chr13:28194470
|
T | A | 88 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.691-2715T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194470 | ||||||
| chr13:28194471
|
T | A | 16 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0002g0145others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.691-2714T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194471 | ||||||
| chr13:28194472
|
T | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0140a0001c0001t0004g0065others(4): Show | 7 | HG00735.hp2 HG01261.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-2713T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194472 | ||||||
| chr13:28194473
|
T | A | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.691-2712T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194473 | ||||||
| chr13:28194475
|
T | A | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.691-2710T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194475 | ||||||
| chr13:28194546
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.691-2639A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194546 | ||||||
| chr13:28194699
|
A | C | 1 | a0001c0001t0005g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.691-2486A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194699 | ||||||
| chr13:28194722
|
C | T | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.691-2463C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194722 | ||||||
| chr13:28194763
|
C | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-2422C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194763 | ||||||
| chr13:28194790
|
T | C | 2 | a0001c0001t0023g0171a0001c0001t0024g0226 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.691-2395T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194790 | ||||||
| chr13:28194879
|
C | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.691-2306C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28194879 | ||||||
| chr13:28194970
|
ACTTATT | A | 14 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(11): Show | 14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.691-2207_691-2202d others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28194970 | |||||
| chr13:28195056
|
T | G | 5 | a0001c0002t0012g0162a0001c0002t0012g0209a0001c0002t0012g0211others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-2129T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28195056 | ||||||
| chr13:28195114
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.691-2071A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28195114 | ||||||
| chr13:28195310
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.691-1875G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28195310 | ||||||
| chr13:28195692
|
T | A | 1 | a0001c0001t0002g0166 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.691-1493T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28195692 | ||||||
| chr13:28196011
|
T | C | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.691-1174T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196011 | ||||||
| chr13:28196026
|
G | GT | 6 | a0001c0001t0001g0155a0001c0001t0002g0166a0001c0001t0008g0244others(3): Show | 6 | HG01496.hp2 HG02486.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-1146dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr13 | 28196026 | |||||
| chr13:28196028
|
T | G | 2 | a0001c0001t0016g0040a0001c0001t0036g0041 | 2 | NA18956.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.691-1157T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196028 | ||||||
| chr13:28196279
|
A | G | 8 | a0001c0001t0002g0115a0001c0001t0002g0164a0001c0001t0002g0169others(5): Show | 8 | HG02071.hp1 HG02523.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-906A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196279 | ||||||
| chr13:28196306
|
A | G | 1 | a0001c0001t0002g0166 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.691-879A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196306 | ||||||
| chr13:28196321
|
G | A | 144 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(141): Show | 144 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.691-864G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196321 | ||||||
| chr13:28196348
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.691-837A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196348 | ||||||
| chr13:28196353
|
G | T | 2 | a0001c0001t0001g0155a0001c0001t0049g0154 | 2 | HG01496.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.691-832G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196353 | ||||||
| chr13:28196468
|
T | G | 2 | a0001c0001t0016g0040a0001c0001t0036g0041 | 2 | NA18956.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.691-717T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196468 | ||||||
| chr13:28196531
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.691-654C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28196531 | ||||||
| chr13:28197111
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.691-74A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 4/18 | chr13 | 28197111 | ||||||
| chr13:28197472
|
T | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.852+126T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197472 | ||||||
| chr13:28197484
|
A | G | 57 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(54): Show | 57 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.852+138A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197484 | ||||||
| chr13:28197512
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.852+166A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197512 | ||||||
| chr13:28197628
|
A | G | 5 | a0001c0001t0008g0007a0001c0001t0008g0245a0001c0001t0008g0246others(2): Show | 5 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+282A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197628 | ||||||
| chr13:28197674
|
G | C | 1 | a0001c0001t0001g0101 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.852+328G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197674 | ||||||
| chr13:28197994
|
C | T | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.852+648C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28197994 | ||||||
| chr13:28198124
|
G | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+778G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198124 | ||||||
| chr13:28198126
|
A | G | 2 | a0001c0001t0006g0030a0001c0001t0045g0102 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.852+780A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198126 | ||||||
| chr13:28198218
|
G | A | 2 | a0001c0001t0005g0182a0001c0001t0007g0183 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.852+872G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198218 | ||||||
| chr13:28198289
|
C | CA | 42 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(39): Show | 42 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.852+956dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28198289 | |||||
| chr13:28198410
|
A | G | 2 | a0001c0001t0011g0184a0001c0001t0019g0185 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852+1064A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198410 | ||||||
| chr13:28198655
|
T | C | 36 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(33): Show | 36 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.852+1309T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198655 | ||||||
| chr13:28198737
|
G | A | 4 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(1): Show | 4 | HG01891.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+1391G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28198737 | ||||||
| chr13:28199127
|
C | T | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+1781C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199127 | ||||||
| chr13:28199231
|
G | T | 56 | a0001c0001t0001g0213a0001c0001t0002g0010a0001c0001t0002g0012others(53): Show | 56 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.852+1885G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199231 | ||||||
| chr13:28199325
|
T | C | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.852+1979T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199325 | ||||||
| chr13:28199333
|
T | A | 1 | a0001c0001t0003g0235 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.852+1987T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199333 | ||||||
| chr13:28199467
|
T | G | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+2121T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199467 | ||||||
| chr13:28199498
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.852+2152C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199498 | ||||||
| chr13:28199503
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.852+2157G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199503 | ||||||
| chr13:28199628
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.852+2282G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199628 | ||||||
| chr13:28199720
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.852+2374A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199720 | ||||||
| chr13:28199727
|
C | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+2381C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199727 | ||||||
| chr13:28199853
|
C | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.852+2507C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28199853 | ||||||
| chr13:28200263
|
ACT | A | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+2920_852+2921d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28200263 | |||||
| chr13:28200360
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+3014T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200360 | ||||||
| chr13:28200421
|
G | A | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+3075G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200421 | ||||||
| chr13:28200501
|
A | G | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.852+3155A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200501 | ||||||
| chr13:28200525
|
C | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+3179C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200525 | ||||||
| chr13:28200607
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.852+3261A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200607 | ||||||
| chr13:28200759
|
A | G | 9 | a0001c0001t0002g0115a0001c0001t0002g0164a0001c0001t0002g0169others(6): Show | 9 | HG02071.hp1 HG02155.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.852+3413A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200759 | ||||||
| chr13:28200770
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.852+3424T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200770 | ||||||
| chr13:28200972
|
G | A | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+3626G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28200972 | ||||||
| chr13:28201078
|
G | A | 3 | a0001c0001t0025g0203a0001c0001t0038g0243a0001c0007t0021g0151 | 3 | HG01358.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.852+3732G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201078 | ||||||
| chr13:28201097
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.852+3751A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201097 | ||||||
| chr13:28201159
|
C | T | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.852+3813C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201159 | ||||||
| chr13:28201174
|
G | A | 33 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(30): Show | 33 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.852+3828G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201174 | ||||||
| chr13:28201201
|
A | AT | 7 | a0001c0001t0010g0121a0001c0001t0010g0124a0001c0001t0010g0126others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+3870dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28201201 | |||||
| chr13:28201403
|
G | A | 2 | a0001c0001t0038g0243a0001c0007t0021g0151 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.852+4057G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201403 | ||||||
| chr13:28201414
|
C | T | 2 | a0001c0001t0023g0171a0001c0001t0024g0226 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.852+4068C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201414 | ||||||
| chr13:28201461
|
G | T | 2 | a0001c0003t0001g0136a0001c0003t0004g0135 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.852+4115G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201461 | ||||||
| chr13:28201487
|
A | C | 3 | a0001c0001t0002g0201a0001c0001t0002g0236a0001c0001t0003g0235 | 3 | NA19062.hp2 NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.852+4141A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201487 | ||||||
| chr13:28201533
|
A | G | 145 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(142): Show | 145 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.852+4187A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201533 | ||||||
| chr13:28201584
|
G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.852+4238G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201584 | ||||||
| chr13:28201674
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.852+4328A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201674 | ||||||
| chr13:28201700
|
G | C | 146 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(143): Show | 146 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.852+4354G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201700 | ||||||
| chr13:28201727
|
G | A | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.852+4381G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201727 | ||||||
| chr13:28201825
|
T | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+4479T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201825 | ||||||
| chr13:28201904
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+4558A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201904 | ||||||
| chr13:28201917
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.852+4571C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28201917 | ||||||
| chr13:28202052
|
AT | A | 14 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(11): Show | 14 | HG01496.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.852+4716delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28202052 | |||||
| chr13:28202062
|
T | C | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+4716T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202062 | ||||||
| chr13:28202320
|
T | A | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.852+4974T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202320 | ||||||
| chr13:28202359
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+5013A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202359 | ||||||
| chr13:28202409
|
T | C | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+5063T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202409 | ||||||
| chr13:28202494
|
G | A | 146 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(143): Show | 146 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.852+5148G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202494 | ||||||
| chr13:28202509
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.852+5163T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202509 | ||||||
| chr13:28202568
|
T | C | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.852+5222T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202568 | ||||||
| chr13:28202658
|
T | TAC | 16 | a0001c0001t0001g0156a0001c0001t0002g0002a0001c0001t0003g0001others(13): Show | 16 | HG00099.hp1 HG01358.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.852+5332_852+5333d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28202658 | |||||
| chr13:28202658
|
T | TACACACA others(1): Show |
3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+5326_852+5333d others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28202658 | |||||
| chr13:28202683
|
T | C | 1 | a0001c0001t0004g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.852+5337T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202683 | ||||||
| chr13:28202704
|
C | T | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.852+5358C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202704 | ||||||
| chr13:28202797
|
A | G | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.852+5451A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202797 | ||||||
| chr13:28202933
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+5587C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202933 | ||||||
| chr13:28202997
|
C | G | 1 | a0001c0001t0007g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.852+5651C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28202997 | ||||||
| chr13:28203041
|
C | A | 2 | a0001c0001t0001g0071a0001c0001t0004g0090 | 2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.852+5695C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203041 | ||||||
| chr13:28203365
|
A | G | 2 | a0001c0001t0050g0050a0001c0001t0051g0095 | 2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.852+6019A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203365 | ||||||
| chr13:28203476
|
C | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+6130C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203476 | ||||||
| chr13:28203680
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0034 | 2 | HG01099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.852+6334A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203680 | ||||||
| chr13:28203704
|
G | A | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.852+6358G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203704 | ||||||
| chr13:28203726
|
T | C | 2 | a0001c0001t0031g0223a0001c0001t0032g0225 | 2 | HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.852+6380T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203726 | ||||||
| chr13:28203756
|
C | T | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.852+6410C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203756 | ||||||
| chr13:28203783
|
G | A | 2 | a0001c0001t0002g0227a0001c0001t0022g0228 | 2 | HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.852+6437G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203783 | ||||||
| chr13:28203807
|
CT | C | 7 | a0001c0001t0001g0069a0001c0001t0004g0099a0001c0001t0017g0204others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+6476delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28203807 | |||||
| chr13:28203811
|
T | C | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+6465T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203811 | ||||||
| chr13:28203812
|
T | C | 79 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(76): Show | 79 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.852+6466T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203812 | ||||||
| chr13:28203950
|
A | G | 8 | a0001c0001t0001g0108a0001c0001t0010g0124a0001c0001t0010g0126others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.852+6604A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203950 | ||||||
| chr13:28203959
|
C | T | 6 | a0001c0001t0015g0250a0001c0001t0029g0249a0001c0001t0039g0005others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.852+6613C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28203959 | ||||||
| chr13:28204519
|
A | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+7173A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28204519 | ||||||
| chr13:28204772
|
A | G | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.852+7426A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28204772 | ||||||
| chr13:28205258
|
T | G | 94 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(91): Show | 94 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.852+7912T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205258 | ||||||
| chr13:28205340
|
A | G | 60 | a0001c0001t0001g0106a0001c0001t0001g0213a0001c0001t0002g0010others(57): Show | 60 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.852+7994A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205340 | ||||||
| chr13:28205372
|
C | G | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.852+8026C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205372 | ||||||
| chr13:28205627
|
C | T | 1 | a0001c0001t0014g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.852+8281C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205627 | ||||||
| chr13:28205741
|
G | A | 1 | a0001c0001t0008g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.852+8395G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205741 | ||||||
| chr13:28205861
|
TA | T | 14 | a0001c0001t0001g0027a0001c0001t0001g0060a0001c0001t0001g0061others(11): Show | 14 | HG02015.hp1 HG02698.hp2 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.852+8531delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28205861 | |||||
| chr13:28205873
|
A | G | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.852+8527A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28205873 | ||||||
| chr13:28206029
|
C | T | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.852+8683C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206029 | ||||||
| chr13:28206121
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.852+8775A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206121 | ||||||
| chr13:28206207
|
A | C | 1 | a0001c0001t0004g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.852+8861A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206207 | ||||||
| chr13:28206253
|
A | T | 2 | a0001c0001t0001g0071a0001c0001t0004g0090 | 2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.852+8907A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206253 | ||||||
| chr13:28206264
|
T | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+8918T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206264 | ||||||
| chr13:28206305
|
G | A | 1 | a0001c0001t0014g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.852+8959G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206305 | ||||||
| chr13:28206315
|
C | CT | 67 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0025others(64): Show | 67 | HG00597.hp1 HG00735.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.852+8993dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28206315 | |||||
| chr13:28206315
|
C | CTT | 5 | a0001c0001t0002g0002a0001c0001t0003g0001a0001c0001t0003g0003others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.852+8992_852+8993d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28206315 | |||||
| chr13:28206315
|
CT | C | 8 | a0001c0001t0001g0045a0001c0001t0002g0197a0001c0001t0002g0217others(5): Show | 8 | HG01358.hp2 HG02258.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.852+8993delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28206315 | |||||
| chr13:28206315
|
CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.852+8986_852+8993d others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28206315 | |||||
| chr13:28206349
|
T | G | 1 | a0001c0001t0005g0180 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.852+9003T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206349 | ||||||
| chr13:28206473
|
C | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.852+9127C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28206473 | ||||||
| chr13:28206738
|
G | GT | 51 | a0001c0001t0002g0166a0001c0001t0002g0200a0001c0001t0003g0009others(48): Show | 51 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.852+9404dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28206738 | |||||
| chr13:28207081
|
G | T | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.852+9735G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207081 | ||||||
| chr13:28207113
|
T | C | 59 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(56): Show | 59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.852+9767T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207113 | ||||||
| chr13:28207188
|
A | G | 2 | a0001c0001t0003g0142a0001c0001t0003g0147 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.852+9842A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207188 | ||||||
| chr13:28207362
|
C | G | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.852+10016C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207362 | ||||||
| chr13:28207418
|
C | T | 14 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(11): Show | 14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.852+10072C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207418 | ||||||
| chr13:28207442
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.852+10096A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207442 | ||||||
| chr13:28207625
|
GTCTTT | G | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.852+10281_852+1028 others(9): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28207625 | |||||
| chr13:28207638
|
G | C | 59 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(56): Show | 59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.852+10292G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207638 | ||||||
| chr13:28207659
|
T | C | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+10313T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28207659 | ||||||
| chr13:28208047
|
A | G | 1 | a0001c0001t0007g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.852+10701A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208047 | ||||||
| chr13:28208345
|
A | T | 1 | a0001c0001t0010g0122 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.852+10999A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208345 | ||||||
| chr13:28208380
|
A | C | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852+11034A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208380 | ||||||
| chr13:28208450
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.852+11104A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208450 | ||||||
| chr13:28208465
|
G | T | 1 | a0001c0001t0011g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.852+11119G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208465 | ||||||
| chr13:28208467
|
T | G | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.852+11121T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208467 | ||||||
| chr13:28208538
|
T | G | 2 | a0001c0001t0001g0054a0001c0001t0004g0055 | 2 | HG02165.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.852+11192T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208538 | ||||||
| chr13:28208546
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.852+11200A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208546 | ||||||
| chr13:28208581
|
C | G | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.852+11235C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208581 | ||||||
| chr13:28208582
|
C | T | 3 | a0001c0001t0025g0203a0001c0001t0038g0243a0001c0007t0021g0151 | 3 | HG01358.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.852+11236C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208582 | ||||||
| chr13:28208589
|
G | A | 1 | a0001c0001t0004g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.852+11243G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208589 | ||||||
| chr13:28208599
|
G | A | 6 | a0001c0001t0002g0143a0001c0001t0002g0145a0001c0001t0002g0146others(3): Show | 6 | NA18941.hp2 NA18967.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.852+11253G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208599 | ||||||
| chr13:28208710
|
C | G | 2 | a0001c0001t0008g0245a0001c0001t0008g0246 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.852+11364C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208710 | ||||||
| chr13:28208884
|
T | A | 1 | a0001c0001t0034g0193 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.853-11347T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208884 | ||||||
| chr13:28208922
|
T | G | 2 | a0001c0001t0002g0233a0001c0001t0002g0240 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.853-11309T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28208922 | ||||||
| chr13:28209137
|
G | A | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.853-11094G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209137 | ||||||
| chr13:28209531
|
T | C | 1 | a0001c0001t0041g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.853-10700T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209531 | ||||||
| chr13:28209566
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-10665A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209566 | ||||||
| chr13:28209603
|
A | T | 1 | a0001c0001t0006g0033 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.853-10628A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209603 | ||||||
| chr13:28209751
|
TCCTGCCT others(1): Show |
T | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-10464_853-1045 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28209751 | |||||
| chr13:28209862
|
C | T | 1 | a0001c0001t0005g0180 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.853-10369C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209862 | ||||||
| chr13:28209939
|
C | A | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.853-10292C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28209939 | ||||||
| chr13:28210078
|
G | T | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-10153G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28210078 | ||||||
| chr13:28210306
|
G | A | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-9925G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28210306 | ||||||
| chr13:28210334
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.853-9897G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28210334 | ||||||
| chr13:28210774
|
C | T | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.853-9457C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28210774 | ||||||
| chr13:28211012
|
C | A | 1 | a0001c0001t0046g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.853-9219C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211012 | ||||||
| chr13:28211039
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.853-9192G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211039 | ||||||
| chr13:28211068
|
A | T | 6 | a0001c0001t0001g0022a0001c0001t0017g0204a0001c0001t0017g0205others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-9163A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211068 | ||||||
| chr13:28211069
|
T | A | 3 | a0001c0001t0025g0203a0001c0001t0038g0243a0001c0007t0021g0151 | 3 | HG01358.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.853-9162T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211069 | ||||||
| chr13:28211088
|
A | G | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-9143A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211088 | ||||||
| chr13:28211383
|
T | G | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-8848T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211383 | ||||||
| chr13:28211546
|
T | G | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.853-8685T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211546 | ||||||
| chr13:28211657
|
C | A | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.853-8574C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211657 | ||||||
| chr13:28211768
|
T | C | 1 | a0001c0001t0002g0037 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.853-8463T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211768 | ||||||
| chr13:28211771
|
A | T | 87 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(84): Show | 87 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.853-8460A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211771 | ||||||
| chr13:28211819
|
C | T | 61 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0022others(58): Show | 61 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.853-8412C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28211819 | ||||||
| chr13:28212083
|
A | G | 72 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(69): Show | 72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.853-8148A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212083 | ||||||
| chr13:28212342
|
G | C | 147 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(144): Show | 147 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.853-7889G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212342 | ||||||
| chr13:28212600
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.853-7631T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212600 | ||||||
| chr13:28212710
|
G | A | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7521G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212710 | ||||||
| chr13:28212740
|
A | C | 147 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(144): Show | 147 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.853-7491A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212740 | ||||||
| chr13:28212851
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.853-7380T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28212851 | ||||||
| chr13:28213088
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0003g0001a0001c0001t0003g0003others(1): Show | 4 | HG02622.hp1 HG02895.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-7143G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213088 | ||||||
| chr13:28213205
|
T | C | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.853-7026T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213205 | ||||||
| chr13:28213291
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.853-6940G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213291 | ||||||
| chr13:28213394
|
A | G | 1 | a0001c0001t0016g0196 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.853-6837A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213394 | ||||||
| chr13:28213402
|
A | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.853-6829A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213402 | ||||||
| chr13:28213546
|
C | T | 1 | a0001c0001t0005g0181 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.853-6685C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213546 | ||||||
| chr13:28213639
|
G | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-6592G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213639 | ||||||
| chr13:28213702
|
C | CA | 22 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0100others(19): Show | 22 | HG00639.hp2 HG01167.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.853-6511dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28213702 | |||||
| chr13:28213702
|
C | CAA | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.853-6512_853-6511d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28213702 | |||||
| chr13:28213702
|
C | CAAA | 7 | a0001c0001t0002g0167a0001c0001t0002g0169a0001c0001t0002g0233others(4): Show | 7 | HG02615.hp1 HG03195.hp2 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.853-6513_853-6511d others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28213702 | |||||
| chr13:28213702
|
CA | C | 8 | a0001c0001t0001g0047a0001c0001t0001g0072a0001c0001t0001g0073others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-6511delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28213702 | |||||
| chr13:28213708
|
A | AC | 14 | a0001c0001t0004g0052a0001c0001t0006g0013a0001c0001t0006g0016others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-6523_853-6522i others(3): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213708 | ||||||
| chr13:28213709
|
A | C | 1 | a0002c0005t0001g0132 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.853-6522A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213709 | ||||||
| chr13:28213906
|
A | G | 75 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(72): Show | 75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.853-6325A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28213906 | ||||||
| chr13:28214169
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.853-6062A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214169 | ||||||
| chr13:28214255
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.853-5976A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214255 | ||||||
| chr13:28214396
|
GT | G | 14 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-5834delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214396 | ||||||
| chr13:28214406
|
G | A | 146 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(143): Show | 146 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.853-5825G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214406 | ||||||
| chr13:28214609
|
T | A | 56 | a0001c0001t0001g0213a0001c0001t0002g0010a0001c0001t0002g0012others(53): Show | 56 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.853-5622T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214609 | ||||||
| chr13:28214619
|
A | G | 6 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-5612A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214619 | ||||||
| chr13:28214677
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.853-5554A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28214677 | ||||||
| chr13:28215245
|
A | G | 1 | a0001c0001t0003g0003 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.853-4986A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215245 | ||||||
| chr13:28215548
|
TGAACCAT others(13): Show |
T | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.853-4681_853-4662d others(22): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28215548 | |||||
| chr13:28215657
|
T | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0034 | 3 | HG01099.hp2 HG01167.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.853-4574T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215657 | ||||||
| chr13:28215730
|
A | C | 6 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-4501A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215730 | ||||||
| chr13:28215815
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.853-4416G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215815 | ||||||
| chr13:28215960
|
G | C | 88 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(85): Show | 88 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.853-4271G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215960 | ||||||
| chr13:28215982
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.853-4249A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28215982 | ||||||
| chr13:28216104
|
T | TTTAAG | 148 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(145): Show | 148 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.853-4124_853-4123i others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28216104 | |||||
| chr13:28216198
|
A | AG | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-4032dupG | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28216198 | |||||
| chr13:28216199
|
G | GA | 76 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(73): Show | 76 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.853-4020dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28216199 | |||||
| chr13:28216209
|
A | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.853-4022A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28216209 | ||||||
| chr13:28216231
|
T | C | 56 | a0001c0001t0001g0213a0001c0001t0002g0010a0001c0001t0002g0012others(53): Show | 56 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.853-4000T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28216231 | ||||||
| chr13:28216280
|
A | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.853-3951A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28216280 | ||||||
| chr13:28216818
|
T | TA | 133 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(130): Show | 133 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.853-3401dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28216818 | |||||
| chr13:28216918
|
C | A | 1 | a0001c0001t0048g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.853-3313C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28216918 | ||||||
| chr13:28216975
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.853-3256G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28216975 | ||||||
| chr13:28217113
|
C | CA | 73 | a0001c0001t0001g0020a0001c0001t0001g0213a0001c0001t0002g0002others(70): Show | 73 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.853-3104dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217113 | |||||
| chr13:28217113
|
CA | C | 6 | a0001c0001t0005g0179a0001c0001t0007g0178a0001c0001t0015g0250others(3): Show | 6 | HG00735.hp2 HG01433.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-3104delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217113 | |||||
| chr13:28217113
|
CAAAA | C | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-3107_853-3104d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217113 | |||||
| chr13:28217138
|
TACA | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-3086_853-3084d others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217138 | |||||
| chr13:28217290
|
T | C | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.853-2941T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217290 | ||||||
| chr13:28217412
|
C | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-2819C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217412 | ||||||
| chr13:28217580
|
CAAAAAAC others(4): Show |
C | 75 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(72): Show | 75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.853-2633_853-2623d others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217580 | |||||
| chr13:28217587
|
C | CA | 50 | a0001c0001t0001g0093a0001c0001t0005g0117a0001c0001t0005g0172others(47): Show | 50 | HG00099.hp1 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.853-2634dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217587 | |||||
| chr13:28217587
|
C | CAA | 6 | a0001c0001t0005g0206a0001c0001t0008g0007a0001c0001t0008g0245others(3): Show | 6 | HG00639.hp1 HG01496.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-2635_853-2634d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217587 | |||||
| chr13:28217593
|
A | G | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-2638A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217593 | ||||||
| chr13:28217598
|
C | CA | 17 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(14): Show | 17 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.853-2623dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217598 | |||||
| chr13:28217669
|
A | T | 75 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(72): Show | 75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.853-2562A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217669 | ||||||
| chr13:28217842
|
G | GT | 251 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(248): Show |
intron_variant | MODIFIER | c.853-2381dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28217842 | |||||
| chr13:28217857
|
A | T | 2 | a0001c0001t0017g0204a0001c0001t0017g0205 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.853-2374A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217857 | ||||||
| chr13:28217961
|
C | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.853-2270C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28217961 | ||||||
| chr13:28218098
|
T | C | 2 | a0001c0001t0005g0206a0001c0001t0030g0161 | 2 | HG00639.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.853-2133T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28218098 | ||||||
| chr13:28218106
|
T | A | 5 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.853-2125T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28218106 | ||||||
| chr13:28218426
|
AAATC | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-1802_853-1799d others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28218426 | |||||
| chr13:28218588
|
A | G | 1 | a0001c0001t0004g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.853-1643A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28218588 | ||||||
| chr13:28219149
|
A | T | 1 | a0001c0001t0003g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.853-1082A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28219149 | ||||||
| chr13:28219422
|
C | CT | 75 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(72): Show | 75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.853-807dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr13 | 28219422 | |||||
| chr13:28219521
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.853-710A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28219521 | ||||||
| chr13:28219620
|
G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.853-611G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28219620 | ||||||
| chr13:28219781
|
C | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.853-450C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28219781 | ||||||
| chr13:28220011
|
A | C | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.853-220A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28220011 | ||||||
| chr13:28220099
|
C | T | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.853-132C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28220099 | ||||||
| chr13:28220121
|
C | T | 17 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(14): Show | 17 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.853-110C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 5/18 | chr13 | 28220121 | ||||||
| chr13:28220597
|
A | G | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1000+219A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28220597 | ||||||
| chr13:28220824
|
T | C | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000+446T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28220824 | ||||||
| chr13:28221016
|
G | C | 5 | a0001c0001t0008g0007a0001c0001t0008g0245a0001c0001t0008g0246others(2): Show | 5 | HG01496.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000+638G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221016 | ||||||
| chr13:28221071
|
G | C | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+693G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221071 | ||||||
| chr13:28221121
|
A | C | 1 | a0001c0001t0004g0067 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1000+743A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221121 | ||||||
| chr13:28221347
|
TA | T | 55 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(52): Show | 55 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1000+980delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28221347 | |||||
| chr13:28221361
|
G | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+983G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221361 | ||||||
| chr13:28221469
|
G | T | 146 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(143): Show | 146 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.1000+1091G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221469 | ||||||
| chr13:28221473
|
A | G | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1000+1095A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221473 | ||||||
| chr13:28221639
|
C | T | 1 | a0001c0001t0004g0090 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1000+1261C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221639 | ||||||
| chr13:28221685
|
A | G | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000+1307A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221685 | ||||||
| chr13:28221725
|
T | C | 1 | a0001c0001t0002g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1000+1347T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221725 | ||||||
| chr13:28221912
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+1534C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221912 | ||||||
| chr13:28221956
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1000+1578T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28221956 | ||||||
| chr13:28222014
|
T | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1000+1636T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222014 | ||||||
| chr13:28222269
|
T | C | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+1891T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222269 | ||||||
| chr13:28222325
|
CT | C | 4 | a0001c0001t0013g0015a0001c0001t0013g0127a0001c0001t0013g0128others(1): Show | 4 | HG00099.hp2 HG03225.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+1948delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222325 | ||||||
| chr13:28222335
|
A | G | 1 | a0001c0001t0005g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1000+1957A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222335 | ||||||
| chr13:28222459
|
T | C | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000+2081T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222459 | ||||||
| chr13:28222610
|
C | G | 2 | a0001c0001t0017g0204a0001c0001t0017g0205 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1000+2232C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222610 | ||||||
| chr13:28222727
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1000+2349A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222727 | ||||||
| chr13:28222741
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1000+2363C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222741 | ||||||
| chr13:28222784
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1000+2406A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222784 | ||||||
| chr13:28222837
|
C | T | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1000+2459C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222837 | ||||||
| chr13:28222854
|
C | T | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1000+2476C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222854 | ||||||
| chr13:28222936
|
G | A | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+2558G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28222936 | ||||||
| chr13:28223287
|
A | G | 1 | a0001c0001t0013g0015 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1000+2909A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223287 | ||||||
| chr13:28223294
|
T | C | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1000+2916T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223294 | ||||||
| chr13:28223350
|
C | CATAG | 5 | a0001c0001t0001g0138a0001c0001t0001g0156a0001c0001t0004g0153others(2): Show | 5 | HG00438.hp1 NA18941.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000+2972_1000+297 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223350 | ||||||
| chr13:28223351
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1000+2973C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223351 | ||||||
| chr13:28223378
|
A | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+3000A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223378 | ||||||
| chr13:28223549
|
GT | G | 28 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(25): Show | 28 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1000+3182delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223549 | |||||
| chr13:28223586
|
G | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1000+3208G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223586 | ||||||
| chr13:28223832
|
A | G | 1 | a0001c0001t0005g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1000+3454A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223832 | ||||||
| chr13:28223871
|
A | AT | 34 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0029others(31): Show | 34 | HG01081.hp1 HG01109.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.1000+3520dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223871 | |||||
| chr13:28223871
|
A | ATT | 11 | a0001c0001t0001g0020a0001c0001t0001g0080a0001c0001t0001g0084others(8): Show | 11 | HG00735.hp2 HG01361.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000+3519_1000+352 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223871 | |||||
| chr13:28223871
|
AT | A | 73 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0062others(70): Show | 73 | HG00438.hp2 HG00735.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.1000+3520delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223871 | |||||
| chr13:28223871
|
ATT | A | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000+3519_1000+352 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223871 | |||||
| chr13:28223871
|
ATTTTTTT others(1): Show |
A | 18 | a0001c0001t0005g0117a0001c0001t0005g0173a0001c0001t0005g0175others(15): Show | 18 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.1000+3513_1000+352 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28223871 | |||||
| chr13:28223936
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1000+3558G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223936 | ||||||
| chr13:28223970
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+3592G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28223970 | ||||||
| chr13:28224037
|
T | A | 1 | a0001c0001t0013g0015 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1000+3659T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224037 | ||||||
| chr13:28224082
|
A | G | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1000+3704A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224082 | ||||||
| chr13:28224171
|
A | G | 58 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1000+3793A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224171 | ||||||
| chr13:28224187
|
G | A | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1000+3809G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224187 | ||||||
| chr13:28224187
|
G | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+3809G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224187 | ||||||
| chr13:28224269
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1000+3891G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224269 | ||||||
| chr13:28224312
|
T | C | 1 | a0001c0001t0003g0165 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1000+3934T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224312 | ||||||
| chr13:28224380
|
G | C | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1000+4002G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224380 | ||||||
| chr13:28224543
|
T | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+4165T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224543 | ||||||
| chr13:28224587
|
G | T | 20 | a0001c0001t0001g0047a0001c0001t0001g0071a0001c0001t0001g0072others(17): Show | 20 | HG00438.hp1 HG01109.hp2 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.1000+4209G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224587 | ||||||
| chr13:28224727
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1000+4349A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28224727 | ||||||
| chr13:28225238
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+4860G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225238 | ||||||
| chr13:28225258
|
C | T | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+4880C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225258 | ||||||
| chr13:28225398
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+5020T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225398 | ||||||
| chr13:28225437
|
G | A | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+5059G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225437 | ||||||
| chr13:28225543
|
A | G | 2 | a0001c0001t0023g0171a0001c0001t0024g0226 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1000+5165A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225543 | ||||||
| chr13:28225747
|
A | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1000+5369A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225747 | ||||||
| chr13:28225841
|
A | G | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+5463A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28225841 | ||||||
| chr13:28226186
|
G | A | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1000+5808G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28226186 | ||||||
| chr13:28226272
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1000+5894C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28226272 | ||||||
| chr13:28226324
|
C | A | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1000+5946C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28226324 | ||||||
| chr13:28226630
|
CTT | C | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1000+6253_1000+625 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28226630 | ||||||
| chr13:28226652
|
T | C | 1 | a0001c0001t0009g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1000+6274T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28226652 | ||||||
| chr13:28227123
|
A | G | 1 | a0001c0001t0004g0051 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1000+6745A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227123 | ||||||
| chr13:28227479
|
C | T | 35 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(32): Show | 35 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1000+7101C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227479 | ||||||
| chr13:28227569
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1000+7191C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227569 | ||||||
| chr13:28227622
|
T | C | 35 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(32): Show | 35 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1000+7244T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227622 | ||||||
| chr13:28227731
|
A | G | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+7353A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227731 | ||||||
| chr13:28227885
|
T | G | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | NA19078.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1000+7507T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227885 | ||||||
| chr13:28227977
|
C | T | 58 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(55): Show | 58 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1000+7599C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28227977 | ||||||
| chr13:28228014
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026 | 3 | HG02886.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1000+7636C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228014 | ||||||
| chr13:28228158
|
T | C | 1 | a0001c0001t0004g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1000+7780T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228158 | ||||||
| chr13:28228217
|
G | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+7839G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228217 | ||||||
| chr13:28228333
|
T | C | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1000+7955T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228333 | ||||||
| chr13:28228497
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1000+8119C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228497 | ||||||
| chr13:28228623
|
CTAG | C | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1000+8250_1000+825 others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28228623 | |||||
| chr13:28228661
|
T | G | 1 | a0001c0001t0006g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1000+8283T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228661 | ||||||
| chr13:28228708
|
C | A | 1 | a0001c0008t0001g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1000+8330C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228708 | ||||||
| chr13:28228768
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+8390C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228768 | ||||||
| chr13:28228772
|
A | G | 5 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+8394A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228772 | ||||||
| chr13:28228887
|
A | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+8509A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228887 | ||||||
| chr13:28228908
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1000+8530A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228908 | ||||||
| chr13:28228995
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1000+8617A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28228995 | ||||||
| chr13:28229096
|
A | G | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1000+8718A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229096 | ||||||
| chr13:28229263
|
T | C | 1 | a0001c0001t0003g0241 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1000+8885T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229263 | ||||||
| chr13:28229445
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1000+9067C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229445 | ||||||
| chr13:28229466
|
C | T | 1 | a0001c0001t0053g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1000+9088C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229466 | ||||||
| chr13:28229499
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+9121T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229499 | ||||||
| chr13:28229570
|
T | G | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1000+9192T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229570 | ||||||
| chr13:28229815
|
G | A | 4 | a0001c0001t0004g0052a0001c0001t0025g0203a0001c0001t0038g0243others(1): Show | 4 | HG01358.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+9437G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229815 | ||||||
| chr13:28229909
|
T | C | 1 | a0001c0001t0013g0015 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1000+9531T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229909 | ||||||
| chr13:28229999
|
C | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+9621C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28229999 | ||||||
| chr13:28230054
|
C | CT | 21 | a0001c0001t0002g0143a0001c0001t0002g0146a0001c0001t0002g0148others(18): Show | 21 | HG00438.hp2 HG02080.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1000+9687dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28230054 | |||||
| chr13:28230054
|
CT | C | 5 | a0001c0001t0001g0076a0001c0001t0015g0250a0001c0001t0029g0249others(2): Show | 5 | HG02602.hp1 HG03098.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+9687delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28230054 | |||||
| chr13:28230272
|
G | T | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1000+9894G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28230272 | ||||||
| chr13:28230352
|
G | C | 3 | a0001c0001t0025g0203a0001c0001t0038g0243a0001c0007t0021g0151 | 3 | HG01358.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1000+9974G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28230352 | ||||||
| chr13:28230544
|
T | A | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1000+10166T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28230544 | ||||||
| chr13:28230787
|
T | TTGAG | 147 | a0001c0001t0001g0066a0001c0001t0001g0107a0001c0001t0001g0130others(144): Show | 147 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.1000+10410_1000+10 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28230787 | |||||
| chr13:28230996
|
G | A | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000+10618G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28230996 | ||||||
| chr13:28231036
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0157 | 2 | NA18961.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1000+10658T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28231036 | ||||||
| chr13:28231264
|
A | G | 3 | a0001c0001t0025g0203a0001c0001t0038g0243a0001c0007t0021g0151 | 3 | HG01358.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1000+10886A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28231264 | ||||||
| chr13:28231344
|
A | AGTT | 3 | a0001c0001t0039g0005a0001c0001t0040g0004a0001c0001t0041g0006 | 3 | HG02257.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1000+10969_1000+10 others(9): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28231344 | |||||
| chr13:28231558
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+11180T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28231558 | ||||||
| chr13:28231975
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+11597A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28231975 | ||||||
| chr13:28232181
|
C | T | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1000+11803C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232181 | ||||||
| chr13:28232287
|
T | C | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1000+11909T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232287 | ||||||
| chr13:28232376
|
C | T | 229 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.1000+11998C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232376 | ||||||
| chr13:28232523
|
C | T | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+12145C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232523 | ||||||
| chr13:28232598
|
C | T | 1 | a0001c0001t0045g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1000+12220C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232598 | ||||||
| chr13:28232654
|
A | G | 59 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(56): Show | 59 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1000+12276A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28232654 | ||||||
| chr13:28233074
|
A | C | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+12696A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233074 | ||||||
| chr13:28233112
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+12734A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233112 | ||||||
| chr13:28233208
|
A | G | 1 | a0001c0001t0002g0038 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1000+12830A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233208 | ||||||
| chr13:28233268
|
CT | C | 9 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0039g0005others(6): Show | 9 | HG02257.hp2 HG02615.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1000+12906delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28233268 | |||||
| chr13:28233459
|
G | T | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13081G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233459 | ||||||
| chr13:28233462
|
T | C | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13084T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233462 | ||||||
| chr13:28233463
|
C | A | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13085C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233463 | ||||||
| chr13:28233483
|
T | A | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13105T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233483 | ||||||
| chr13:28233570
|
A | C | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13192A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233570 | ||||||
| chr13:28233625
|
T | C | 2 | a0001c0001t0013g0015a0001c0001t0046g0035 | 2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1000+13247T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233625 | ||||||
| chr13:28233681
|
A | T | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13303A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233681 | ||||||
| chr13:28233682
|
T | A | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+13304T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233682 | ||||||
| chr13:28233918
|
G | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1000+13540G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28233918 | ||||||
| chr13:28234048
|
T | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+13670T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234048 | ||||||
| chr13:28234163
|
C | A | 1 | a0001c0001t0023g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1000+13785C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234163 | ||||||
| chr13:28234233
|
C | G | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1000+13855C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234233 | ||||||
| chr13:28234275
|
C | T | 1 | a0001c0001t0055g0088 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1000+13897C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234275 | ||||||
| chr13:28234388
|
T | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+14010T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234388 | ||||||
| chr13:28234437
|
T | A | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+14059T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234437 | ||||||
| chr13:28234459
|
G | A | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+14081G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234459 | ||||||
| chr13:28234465
|
T | G | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1000+14087T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234465 | ||||||
| chr13:28234490
|
G | T | 3 | a0001c0003t0001g0136a0001c0003t0004g0135a0001c0003t0014g0078 | 3 | HG02922.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1000+14112G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234490 | ||||||
| chr13:28234590
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+14212G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234590 | ||||||
| chr13:28234610
|
A | T | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1000+14232A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234610 | ||||||
| chr13:28234821
|
A | C | 234 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(231): Show |
intron_variant | MODIFIER | c.1000+14443A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234821 | ||||||
| chr13:28234822
|
T | C | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1000+14444T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234822 | ||||||
| chr13:28234968
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1000+14590A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28234968 | ||||||
| chr13:28235620
|
C | A | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1000+15242C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235620 | ||||||
| chr13:28235676
|
C | G | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1000+15298C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235676 | ||||||
| chr13:28235682
|
T | TACACACA others(5): Show |
1 | a0001c0001t0005g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1000+15306_1000+15 others(18): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235682 | |||||
| chr13:28235682
|
T | TACACACA others(7): Show |
1 | a0001c0001t0007g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1000+15317_1000+15 others(20): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235682 | |||||
| chr13:28235682
|
T | TACACACA others(11): Show |
2 | a0001c0001t0005g0188a0001c0001t0007g0177 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1000+15317_1000+15 others(24): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235682 | |||||
| chr13:28235682
|
T | TACACACA others(13): Show |
2 | a0001c0001t0005g0173a0001c0001t0005g0175 | 2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1000+15317_1000+15 others(26): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235682 | |||||
| chr13:28235682
|
T | TACACACA others(9): Show |
1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1000+15313_1000+15 others(22): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235682 | |||||
| chr13:28235688
|
C | CACAT | 10 | a0001c0001t0002g0012a0001c0001t0002g0217a0001c0001t0002g0227others(7): Show | 10 | HG01358.hp2 HG01361.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000+15313_1000+15 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235688 | |||||
| chr13:28235690
|
C | CAT | 55 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(52): Show | 55 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1000+15313_1000+15 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235690 | |||||
| chr13:28235692
|
C | T | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1000+15314C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235692 | ||||||
| chr13:28235696
|
T | C | 76 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(73): Show | 76 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.1000+15318T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235696 | ||||||
| chr13:28235696
|
T | TAC | 104 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(101): Show | 104 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.1000+15344_1000+15 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235696
|
T | TACAC | 11 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(8): Show | 11 | HG00438.hp1 HG01175.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000+15342_1000+15 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235696
|
T | TACACAC | 21 | a0001c0001t0005g0179a0001c0001t0005g0181a0001c0001t0005g0182others(18): Show | 21 | HG00597.hp2 HG00639.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1000+15340_1000+15 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235696
|
T | TACACACA others(1): Show |
11 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0180others(8): Show | 11 | HG00099.hp1 HG01099.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000+15338_1000+15 others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235696
|
T | TACACACA others(3): Show |
3 | a0001c0001t0011g0184a0001c0001t0019g0185a0001c0001t0038g0243 | 3 | HG02109.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1000+15336_1000+15 others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235696
|
T | TACACACA others(5): Show |
3 | a0001c0001t0008g0007a0001c0001t0024g0226a0001c0001t0031g0223 | 3 | HG02145.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1000+15334_1000+15 others(18): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235696
|
T | TACACACA others(9): Show |
1 | a0001c0001t0010g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1000+15330_1000+15 others(22): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235696
|
T | TACACACA others(11): Show |
1 | a0001c0001t0010g0122 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1000+15328_1000+15 others(24): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235696
|
T | TACACACA others(13): Show |
4 | a0001c0001t0010g0121a0001c0001t0010g0152a0001c0001t0028g0125others(1): Show | 4 | HG02109.hp2 HG02809.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+15326_1000+15 others(26): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235696
|
T | TACACACA others(17): Show |
1 | a0001c0001t0010g0124 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1000+15322_1000+15 others(30): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235696
|
T | TACACACA others(33): Show |
1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1000+15345_1000+15 others(46): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235696 | |||||
| chr13:28235722
|
C | CACACACA others(11): Show |
1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1000+15345_1000+15 others(24): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235722 | |||||
| chr13:28235722
|
C | CACACACA others(3): Show |
1 | a0001c0001t0017g0204 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1000+15345_1000+15 others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235722 | |||||
| chr13:28235722
|
C | CACACAT | 4 | a0001c0001t0001g0156a0001c0001t0004g0153a0001c0001t0004g0158others(1): Show | 4 | NA18941.hp1 NA18998.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+15345_1000+15 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235722 | |||||
| chr13:28235724
|
T | C | 103 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(100): Show | 103 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1000+15346T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235724 | ||||||
| chr13:28235726
|
T | C | 16 | a0001c0001t0002g0227a0001c0001t0005g0172a0001c0001t0005g0173others(13): Show | 16 | HG00639.hp2 HG01175.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1000+15348T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235726 | ||||||
| chr13:28235728
|
T | C | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1000+15350T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235728 | ||||||
| chr13:28235729
|
A | T | 1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+15351A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235729 | ||||||
| chr13:28235768
|
G | A | 1 | a0001c0001t0004g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1000+15390G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28235768 | ||||||
| chr13:28235886
|
A | AT | 6 | a0001c0001t0001g0139a0001c0001t0004g0090a0001c0001t0004g0109others(3): Show | 6 | HG03098.hp2 HG03831.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+15525dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235886 | |||||
| chr13:28235886
|
AT | A | 73 | a0001c0001t0001g0028a0001c0001t0001g0062a0001c0001t0001g0213others(70): Show | 73 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.1000+15525delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28235886 | |||||
| chr13:28236003
|
A | ATTAC | 3 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0147 | 3 | HG01069.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1000+15626_1000+15 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28236003 | |||||
| chr13:28236103
|
G | A | 107 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(104): Show | 107 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.1000+15725G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236103 | ||||||
| chr13:28236249
|
G | A | 1 | a0001c0001t0017g0204 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1000+15871G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236249 | ||||||
| chr13:28236285
|
A | G | 3 | a0001c0001t0002g0002a0001c0001t0003g0001a0001c0001t0003g0003 | 3 | HG02622.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1000+15907A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236285 | ||||||
| chr13:28236420
|
T | C | 2 | a0001c0001t0013g0015a0001c0001t0046g0035 | 2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1000+16042T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236420 | ||||||
| chr13:28236634
|
T | G | 1 | a0001c0001t0001g0025 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1000+16256T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236634 | ||||||
| chr13:28236729
|
A | G | 32 | a0001c0001t0001g0213a0001c0001t0002g0010a0001c0001t0002g0012others(29): Show | 32 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1000+16351A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28236729 | ||||||
| chr13:28237195
|
AT | A | 221 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(218): Show | 221 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(218): Show |
intron_variant | MODIFIER | c.1000+16829delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28237195 | |||||
| chr13:28237195
|
ATT | A | 23 | a0001c0001t0001g0118a0001c0001t0002g0012a0001c0001t0005g0117others(20): Show | 23 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1000+16828_1000+16 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28237195 | |||||
| chr13:28237219
|
A | G | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+16841A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28237219 | ||||||
| chr13:28237239
|
A | C | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1000+16861A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28237239 | ||||||
| chr13:28237535
|
G | A | 1 | a0001c0001t0025g0203 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1000+17157G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28237535 | ||||||
| chr13:28237742
|
T | C | 73 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(70): Show | 73 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.1000+17364T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28237742 | ||||||
| chr13:28237887
|
CAA | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1000+17510_1000+17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28237887 | ||||||
| chr13:28238068
|
C | A | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1000+17690C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238068 | ||||||
| chr13:28238075
|
C | T | 2 | a0001c0001t0003g0216a0001c0001t0003g0218 | 2 | NA19082.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1000+17697C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238075 | ||||||
| chr13:28238171
|
A | G | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1000+17793A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238171 | ||||||
| chr13:28238186
|
T | TGGAAGGC others(4): Show |
1 | a0001c0001t0002g0012 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1000+17810_1000+17 others(17): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28238186 | |||||
| chr13:28238417
|
C | A | 86 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(83): Show | 86 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.1001-17875C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238417 | ||||||
| chr13:28238446
|
T | G | 20 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(17): Show | 20 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1001-17846T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238446 | ||||||
| chr13:28238541
|
A | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-17751A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238541 | ||||||
| chr13:28238562
|
T | C | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001-17730T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238562 | ||||||
| chr13:28238692
|
C | T | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-17600C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238692 | ||||||
| chr13:28238693
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1001-17599G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238693 | ||||||
| chr13:28238762
|
T | C | 1 | a0001c0001t0006g0016 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1001-17530T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238762 | ||||||
| chr13:28238820
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1001-17472A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238820 | ||||||
| chr13:28238917
|
T | G | 3 | a0001c0001t0003g0214a0001c0001t0009g0189a0001c0001t0047g0019 | 3 | HG01167.hp2 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1001-17375T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238917 | ||||||
| chr13:28238956
|
G | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-17336G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238956 | ||||||
| chr13:28238987
|
A | G | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1001-17305A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28238987 | ||||||
| chr13:28239137
|
A | AC | 17 | a0001c0001t0001g0014a0001c0001t0001g0061a0001c0001t0001g0072others(14): Show | 17 | HG01099.hp2 HG01361.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1001-17147dupC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239137 | |||||
| chr13:28239146
|
A | C | 2 | a0001c0001t0005g0117a0001c0009t0001g0063 | 2 | HG02056.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1001-17146A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28239146 | ||||||
| chr13:28239151
|
C | A | 1 | a0001c0001t0002g0145 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1001-17141C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28239151 | ||||||
| chr13:28239162
|
A | AAC | 58 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0115others(55): Show | 58 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.1001-17105_1001-17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | |||||
| chr13:28239162
|
A | AACAC | 30 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0130others(27): Show | 30 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1001-17107_1001-17 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | |||||
| chr13:28239162
|
A | AACACAC | 88 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(85): Show | 88 | HG00099.hp2 HG01081.hp1 HG01099.hp2 others(85): Show |
intron_variant | MODIFIER | c.1001-17109_1001-17 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | |||||
| chr13:28239162
|
A | AACACACA others(1): Show |
29 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(26): Show | 29 | HG00438.hp1 HG00735.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1001-17111_1001-17 others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | |||||
| chr13:28239162
|
A | AACACACA others(3): Show |
6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-17113_1001-17 others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | |||||
| chr13:28239162
|
AAC | A | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1001-17105_1001-17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | |||||
| chr13:28239162
|
AACAC | A | 7 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(4): Show | 7 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1001-17107_1001-17 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239162 | |||||
| chr13:28239192
|
T | TGCACACA others(3): Show |
1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1001-17099_1001-17 others(16): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239192 | |||||
| chr13:28239199
|
A | ACG | 11 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(8): Show | 11 | HG00099.hp1 HG00597.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1001-17091_1001-17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239199 | |||||
| chr13:28239199
|
A | ACGCG | 12 | a0001c0001t0005g0172a0001c0001t0011g0184a0001c0001t0011g0187others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1001-17090_1001-17 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239199 | |||||
| chr13:28239201
|
G | GCA | 12 | a0001c0001t0002g0233a0001c0001t0002g0240a0001c0001t0003g0214others(9): Show | 12 | HG01167.hp2 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1001-17071_1001-17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239201 | |||||
| chr13:28239201
|
G | GCGCA | 7 | a0001c0001t0005g0173a0001c0001t0005g0175a0001c0001t0005g0188others(4): Show | 7 | HG00639.hp1 HG00639.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1001-17090_1001-17 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239201 | |||||
| chr13:28239201
|
GCA | G | 5 | a0001c0001t0001g0058a0001c0001t0050g0050a0001c0001t0051g0095others(2): Show | 5 | HG02132.hp1 HG02135.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001-17071_1001-17 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239201 | |||||
| chr13:28239201
|
GCACA | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-17073_1001-17 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28239201 | |||||
| chr13:28239203
|
A | G | 2 | a0001c0001t0007g0183a0001c0001t0027g0150 | 2 | HG01099.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1001-17089A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28239203 | ||||||
| chr13:28239812
|
A | G | 1 | a0001c0001t0002g0219 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1001-16480A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28239812 | ||||||
| chr13:28239982
|
T | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-16310T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28239982 | ||||||
| chr13:28240233
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-16059A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240233 | ||||||
| chr13:28240450
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1001-15842A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240450 | ||||||
| chr13:28240518
|
A | T | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-15774A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240518 | ||||||
| chr13:28240536
|
C | T | 64 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0022others(61): Show | 64 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(61): Show |
intron_variant | MODIFIER | c.1001-15756C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240536 | ||||||
| chr13:28240876
|
C | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-15416C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240876 | ||||||
| chr13:28240986
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-15306G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28240986 | ||||||
| chr13:28241011
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1001-15281A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241011 | ||||||
| chr13:28241032
|
T | C | 248 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.1001-15260T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241032 | ||||||
| chr13:28241069
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1001-15223T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241069 | ||||||
| chr13:28241139
|
T | C | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1001-15153T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241139 | ||||||
| chr13:28241635
|
TATTA | T | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1001-14653_1001-14 others(10): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28241635 | |||||
| chr13:28241777
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1001-14515C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241777 | ||||||
| chr13:28241878
|
T | C | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001-14414T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241878 | ||||||
| chr13:28241908
|
T | TGACATAT others(25): Show |
1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1001-14383_1001-14 others(38): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28241908 | |||||
| chr13:28241967
|
C | T | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1001-14325C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241967 | ||||||
| chr13:28241982
|
G | C | 5 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-14310G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28241982 | ||||||
| chr13:28242141
|
G | A | 115 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(112): Show | 115 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1001-14151G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242141 | ||||||
| chr13:28242188
|
T | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1001-14104T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242188 | ||||||
| chr13:28242206
|
A | G | 1 | a0001c0001t0004g0043 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1001-14086A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242206 | ||||||
| chr13:28242240
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1001-14052A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242240 | ||||||
| chr13:28242267
|
G | A | 44 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(41): Show | 44 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1001-14025G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242267 | ||||||
| chr13:28242283
|
G | T | 22 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(19): Show | 22 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1001-14009G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242283 | ||||||
| chr13:28242326
|
CTTGGTTG | C | 5 | a0001c0002t0012g0162a0001c0002t0012g0209a0001c0002t0012g0211others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-13960_1001-13 others(13): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28242326 | |||||
| chr13:28242625
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-13667A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242625 | ||||||
| chr13:28242674
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1001-13618G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242674 | ||||||
| chr13:28242781
|
A | G | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1001-13511A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242781 | ||||||
| chr13:28242913
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-13379C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28242913 | ||||||
| chr13:28243025
|
T | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-13267T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243025 | ||||||
| chr13:28243032
|
C | T | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1001-13260C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243032 | ||||||
| chr13:28243264
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-13028A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243264 | ||||||
| chr13:28243395
|
G | C | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1001-12897G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243395 | ||||||
| chr13:28243400
|
A | C | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1001-12892A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243400 | ||||||
| chr13:28243632
|
C | T | 1 | a0001c0001t0009g0220 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1001-12660C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243632 | ||||||
| chr13:28243684
|
G | A | 1 | a0001c0001t0009g0220 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1001-12608G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243684 | ||||||
| chr13:28243743
|
T | C | 248 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.1001-12549T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243743 | ||||||
| chr13:28243788
|
C | T | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1001-12504C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243788 | ||||||
| chr13:28243846
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-12446G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243846 | ||||||
| chr13:28243860
|
T | C | 65 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(62): Show | 65 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(62): Show |
intron_variant | MODIFIER | c.1001-12432T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28243860 | ||||||
| chr13:28244163
|
G | T | 248 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.1001-12129G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244163 | ||||||
| chr13:28244273
|
C | T | 2 | a0001c0001t0023g0171a0001c0001t0024g0226 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1001-12019C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244273 | ||||||
| chr13:28244511
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1001-11781T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244511 | ||||||
| chr13:28244579
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0157 | 2 | NA18961.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1001-11713C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244579 | ||||||
| chr13:28244581
|
G | T | 2 | a0001c0003t0001g0136a0001c0003t0004g0135 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1001-11711G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244581 | ||||||
| chr13:28244604
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0004g0090 | 2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1001-11688A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244604 | ||||||
| chr13:28244682
|
T | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1001-11610T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244682 | ||||||
| chr13:28244759
|
CAGT | C | 248 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.1001-11526_1001-11 others(9): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28244759 | |||||
| chr13:28244798
|
T | C | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-11494T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244798 | ||||||
| chr13:28244910
|
G | A | 1 | a0002c0005t0001g0132 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1001-11382G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28244910 | ||||||
| chr13:28245115
|
G | C | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1001-11177G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28245115 | ||||||
| chr13:28245370
|
C | T | 14 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(11): Show | 14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.1001-10922C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28245370 | ||||||
| chr13:28245391
|
C | CT | 14 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(11): Show | 14 | HG01099.hp1 HG01109.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1001-10890dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28245391 | |||||
| chr13:28245391
|
C | CTT | 20 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(17): Show | 20 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1001-10891_1001-10 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28245391 | |||||
| chr13:28245721
|
AC | A | 5 | a0001c0002t0012g0162a0001c0002t0012g0209a0001c0002t0012g0211others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-10570delC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28245721 | ||||||
| chr13:28245767
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-10525C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28245767 | ||||||
| chr13:28245973
|
A | G | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1001-10319A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28245973 | ||||||
| chr13:28246389
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-9903A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246389 | ||||||
| chr13:28246473
|
C | A | 106 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(103): Show | 106 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(103): Show |
intron_variant | MODIFIER | c.1001-9819C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246473 | ||||||
| chr13:28246473
|
C | T | 142 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0213others(139): Show | 142 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.1001-9819C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246473 | ||||||
| chr13:28246638
|
A | G | 1 | a0001c0001t0009g0220 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1001-9654A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246638 | ||||||
| chr13:28246658
|
T | C | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1001-9634T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246658 | ||||||
| chr13:28246796
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0004g0090 | 2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1001-9496A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246796 | ||||||
| chr13:28246856
|
C | T | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-9436C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246856 | ||||||
| chr13:28246900
|
C | T | 1 | a0001c0001t0053g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1001-9392C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28246900 | ||||||
| chr13:28247136
|
T | C | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-9156T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247136 | ||||||
| chr13:28247180
|
C | CT | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1001-9106dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28247180 | |||||
| chr13:28247261
|
C | A | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1001-9031C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247261 | ||||||
| chr13:28247267
|
G | C | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1001-9025G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247267 | ||||||
| chr13:28247343
|
G | A | 1 | a0001c0001t0003g0009 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1001-8949G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247343 | ||||||
| chr13:28247394
|
C | G | 2 | a0001c0001t0023g0171a0001c0001t0024g0226 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1001-8898C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247394 | ||||||
| chr13:28247416
|
G | T | 248 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.1001-8876G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247416 | ||||||
| chr13:28247603
|
A | G | 1 | a0001c0001t0009g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1001-8689A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247603 | ||||||
| chr13:28247816
|
C | T | 2 | a0001c0001t0017g0204a0001c0001t0017g0205 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1001-8476C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247816 | ||||||
| chr13:28247822
|
C | T | 1 | a0001c0001t0004g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1001-8470C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247822 | ||||||
| chr13:28247974
|
A | G | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1001-8318A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28247974 | ||||||
| chr13:28248127
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-8165T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248127 | ||||||
| chr13:28248242
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1001-8050G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248242 | ||||||
| chr13:28248383
|
G | C | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001-7909G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248383 | ||||||
| chr13:28248517
|
G | A | 1 | a0001c0001t0048g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1001-7775G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248517 | ||||||
| chr13:28248520
|
CT | C | 247 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1001-7762delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28248520 | |||||
| chr13:28248979
|
C | A | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1001-7313C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248979 | ||||||
| chr13:28248985
|
T | G | 1 | a0001c0001t0004g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1001-7307T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28248985 | ||||||
| chr13:28249095
|
A | T | 92 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(89): Show | 92 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(89): Show |
intron_variant | MODIFIER | c.1001-7197A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249095 | ||||||
| chr13:28249133
|
A | G | 2 | a0001c0001t0010g0121a0001c0001t0010g0122 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1001-7159A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249133 | ||||||
| chr13:28249140
|
A | G | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1001-7152A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249140 | ||||||
| chr13:28249157
|
T | C | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-7135T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249157 | ||||||
| chr13:28249356
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1001-6936T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249356 | ||||||
| chr13:28249439
|
A | G | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001-6853A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249439 | ||||||
| chr13:28249518
|
G | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-6774G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249518 | ||||||
| chr13:28249531
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-6761C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249531 | ||||||
| chr13:28249532
|
T | G | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001-6760T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249532 | ||||||
| chr13:28249741
|
C | T | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1001-6551C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249741 | ||||||
| chr13:28249848
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1001-6444A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28249848 | ||||||
| chr13:28250056
|
T | C | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-6236T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250056 | ||||||
| chr13:28250076
|
G | A | 2 | a0001c0001t0011g0184a0001c0001t0019g0185 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1001-6216G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250076 | ||||||
| chr13:28250129
|
A | G | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1001-6163A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250129 | ||||||
| chr13:28250183
|
C | T | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001-6109C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250183 | ||||||
| chr13:28250194
|
C | G | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1001-6098C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250194 | ||||||
| chr13:28250201
|
C | CT | 10 | a0001c0001t0001g0081a0001c0001t0010g0121a0001c0001t0010g0122others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1001-6077dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28250201 | |||||
| chr13:28250201
|
C | CTT | 6 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001-6078_1001-607 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28250201 | |||||
| chr13:28250201
|
C | CTTT | 5 | a0001c0002t0012g0162a0001c0002t0012g0209a0001c0002t0012g0211others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-6079_1001-607 others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28250201 | |||||
| chr13:28250203
|
T | G | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | NA19078.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1001-6089T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250203 | ||||||
| chr13:28250314
|
G | T | 106 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(103): Show | 106 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(103): Show |
intron_variant | MODIFIER | c.1001-5978G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250314 | ||||||
| chr13:28250338
|
G | A | 1 | a0001c0001t0003g0168 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1001-5954G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250338 | ||||||
| chr13:28250390
|
G | A | 104 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(101): Show | 104 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.1001-5902G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250390 | ||||||
| chr13:28250590
|
C | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-5702C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250590 | ||||||
| chr13:28250618
|
C | T | 120 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(117): Show | 120 | HG00099.hp2 HG00438.hp1 HG00735.hp1 others(117): Show |
intron_variant | MODIFIER | c.1001-5674C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250618 | ||||||
| chr13:28250782
|
G | T | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1001-5510G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250782 | ||||||
| chr13:28250810
|
G | T | 4 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0014g0111others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-5482G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250810 | ||||||
| chr13:28250815
|
C | T | 1 | a0001c0001t0008g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1001-5477C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28250815 | ||||||
| chr13:28251371
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1001-4921G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251371 | ||||||
| chr13:28251479
|
G | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-4813G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251479 | ||||||
| chr13:28251574
|
C | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1001-4718C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251574 | ||||||
| chr13:28251612
|
C | T | 1 | a0001c0001t0005g0182 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1001-4680C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251612 | ||||||
| chr13:28251618
|
C | T | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-4674C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251618 | ||||||
| chr13:28251642
|
A | G | 248 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.1001-4650A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251642 | ||||||
| chr13:28251701
|
G | A | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001-4591G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251701 | ||||||
| chr13:28251772
|
C | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-4520C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251772 | ||||||
| chr13:28251793
|
CT | C | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-4498delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251793 | ||||||
| chr13:28251801
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1001-4491G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251801 | ||||||
| chr13:28251871
|
G | GGTTT | 8 | a0001c0001t0001g0061a0001c0001t0011g0184a0001c0001t0019g0185others(5): Show | 8 | HG01109.hp1 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1001-4418_1001-441 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28251871 | |||||
| chr13:28251875
|
G | GGTTT | 124 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1001-4395_1001-439 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28251875 | |||||
| chr13:28251875
|
G | GGTTTGTT others(1): Show |
6 | a0001c0001t0001g0120a0001c0001t0005g0172a0001c0001t0005g0173others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-4399_1001-439 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28251875 | |||||
| chr13:28251875
|
G | T | 14 | a0001c0001t0001g0061a0001c0001t0011g0184a0001c0001t0011g0187others(11): Show | 14 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1001-4417G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251875 | ||||||
| chr13:28251902
|
T | C | 2 | a0001c0001t0023g0171a0001c0001t0024g0226 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1001-4390T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28251902 | ||||||
| chr13:28252031
|
G | A | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1001-4261G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252031 | ||||||
| chr13:28252116
|
G | C | 1 | a0001c0001t0003g0165 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1001-4176G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252116 | ||||||
| chr13:28252184
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1001-4108G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252184 | ||||||
| chr13:28252188
|
C | CT | 5 | a0001c0001t0001g0081a0001c0001t0001g0093a0001c0001t0029g0249others(2): Show | 5 | HG01175.hp2 HG03098.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001-4082dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28252188 | |||||
| chr13:28252188
|
CT | C | 33 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0106others(30): Show | 33 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1001-4082delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28252188 | |||||
| chr13:28252188
|
CTT | C | 80 | a0001c0001t0001g0213a0001c0001t0002g0010a0001c0001t0002g0012others(77): Show | 80 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.1001-4083_1001-408 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28252188 | |||||
| chr13:28252188
|
CTTT | C | 10 | a0001c0001t0002g0002a0001c0001t0002g0143a0001c0001t0002g0145others(7): Show | 10 | HG02622.hp1 HG02895.hp1 NA18522.hp1 others(7): Show |
intron_variant | MODIFIER | c.1001-4084_1001-408 others(7): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28252188 | |||||
| chr13:28252252
|
C | G | 2 | a0001c0001t0017g0204a0001c0001t0017g0205 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1001-4040C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252252 | ||||||
| chr13:28252299
|
G | A | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1001-3993G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252299 | ||||||
| chr13:28252412
|
T | A | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1001-3880T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252412 | ||||||
| chr13:28252478
|
T | TA | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001-3813dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28252478 | |||||
| chr13:28252761
|
A | G | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1001-3531A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252761 | ||||||
| chr13:28252828
|
A | G | 6 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001-3464A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252828 | ||||||
| chr13:28252846
|
A | G | 94 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(91): Show | 94 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.1001-3446A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252846 | ||||||
| chr13:28252934
|
G | A | 1 | a0001c0001t0004g0051 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1001-3358G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252934 | ||||||
| chr13:28252959
|
C | T | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001-3333C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28252959 | ||||||
| chr13:28253301
|
TA | T | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1001-2989delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28253301 | |||||
| chr13:28253712
|
C | A | 1 | a0001c0001t0010g0152 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1001-2580C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28253712 | ||||||
| chr13:28253713
|
G | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1001-2579G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28253713 | ||||||
| chr13:28253715
|
TC | T | 94 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(91): Show | 94 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.1001-2575delC | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28253715 | |||||
| chr13:28253785
|
T | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001-2507T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28253785 | ||||||
| chr13:28254055
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-2237A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254055 | ||||||
| chr13:28254080
|
G | A | 248 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.1001-2212G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254080 | ||||||
| chr13:28254135
|
C | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-2157C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254135 | ||||||
| chr13:28254279
|
T | C | 1 | a0001c0001t0002g0191 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1001-2013T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254279 | ||||||
| chr13:28254416
|
T | C | 20 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(17): Show | 20 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1001-1876T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254416 | ||||||
| chr13:28254705
|
A | AT | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1001-1579dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr13 | 28254705 | |||||
| chr13:28254756
|
A | G | 4 | a0001c0001t0006g0013a0001c0001t0006g0031a0001c0001t0006g0033others(1): Show | 4 | HG00735.hp1 HG01069.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-1536A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254756 | ||||||
| chr13:28254975
|
C | T | 72 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(69): Show | 72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.1001-1317C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28254975 | ||||||
| chr13:28255085
|
T | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-1207T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255085 | ||||||
| chr13:28255106
|
C | T | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1001-1186C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255106 | ||||||
| chr13:28255139
|
T | G | 1 | a0001c0001t0002g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1001-1153T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255139 | ||||||
| chr13:28255298
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1001-994A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255298 | ||||||
| chr13:28255335
|
T | C | 3 | a0001c0001t0009g0194a0001c0001t0009g0198a0001c0001t0009g0215 | 3 | NA18943.hp2 NA18981.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1001-957T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255335 | ||||||
| chr13:28255527
|
C | T | 95 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(92): Show | 95 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(92): Show |
intron_variant | MODIFIER | c.1001-765C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255527 | ||||||
| chr13:28255855
|
G | A | 4 | a0001c0001t0005g0179a0001c0001t0005g0206a0001c0001t0007g0178others(1): Show | 4 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-437G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255855 | ||||||
| chr13:28255995
|
T | A | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1001-297T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28255995 | ||||||
| chr13:28256275
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0004g0043 | 2 | NA18956.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1001-17T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28256275 | ||||||
| chr13:28256281
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1001-11A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 6/18 | chr13 | 28256281 | ||||||
| chr13:28256860
|
T | G | 98 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(95): Show | 98 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(95): Show |
intron_variant | MODIFIER | c.1248+321T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28256860 | ||||||
| chr13:28256861
|
A | C | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+322A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28256861 | ||||||
| chr13:28257045
|
A | G | 1 | a0003c0006t0015g0251 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1248+506A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257045 | ||||||
| chr13:28257104
|
A | G | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1248+565A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257104 | ||||||
| chr13:28257115
|
A | T | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+576A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257115 | ||||||
| chr13:28257134
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1248+595G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257134 | ||||||
| chr13:28257171
|
T | C | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1248+632T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257171 | ||||||
| chr13:28257278
|
G | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1248+739G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257278 | ||||||
| chr13:28257318
|
G | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+779G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257318 | ||||||
| chr13:28257505
|
G | T | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1248+966G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257505 | ||||||
| chr13:28257559
|
A | G | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1248+1020A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257559 | ||||||
| chr13:28257639
|
A | G | 1 | a0001c0001t0005g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1248+1100A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257639 | ||||||
| chr13:28257687
|
T | TATAAATA others(22): Show |
11 | a0001c0001t0004g0052a0001c0001t0006g0013a0001c0001t0006g0016others(8): Show | 11 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1248+1151_1248+117 others(33): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257687 | |||||
| chr13:28257687
|
T | TATAAATA others(51): Show |
3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0045g0102 | 3 | HG01346.hp2 HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1248+1179_1248+118 others(62): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257687 | |||||
| chr13:28257690
|
A | AAATATAT others(22): Show |
1 | a0001c0001t0001g0066 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1248+1169_1248+119 others(33): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257690 | |||||
| chr13:28257699
|
TTA | T | 2 | a0001c0001t0002g0219a0001c0001t0003g0008 | 2 | HG00438.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1248+1168_1248+116 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257699 | |||||
| chr13:28257701
|
A | ATATATAT others(20): Show |
3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1248+1170_1248+119 others(31): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257701 | |||||
| chr13:28257706
|
T | TATTATAT others(24): Show |
1 | a0001c0001t0007g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1248+1180_1248+121 others(35): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257706 | |||||
| chr13:28257709
|
T | A | 4 | a0001c0001t0005g0173a0001c0001t0005g0175a0001c0001t0005g0188others(1): Show | 4 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+1170T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257709 | ||||||
| chr13:28257721
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0054 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1248+1222_1248+126 others(43): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257721 | |||||
| chr13:28257721
|
ATATATAT others(32): Show |
A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1248+1222_1248+126 others(43): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257721 | |||||
| chr13:28257727
|
ATTATATA others(44): Show |
A | 2 | a0001c0001t0005g0182a0001c0001t0007g0183 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1248+1190_1248+124 others(55): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28257727 | |||||
| chr13:28257737
|
A | T | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+1198A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257737 | ||||||
| chr13:28257758
|
A | ATATATAA others(3): Show |
1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+1219_1248+122 others(14): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257758 | ||||||
| chr13:28257760
|
T | A | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+1221T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257760 | ||||||
| chr13:28257762
|
A | T | 75 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(72): Show | 75 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.1248+1223A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257762 | ||||||
| chr13:28257767
|
T | A | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+1228T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257767 | ||||||
| chr13:28257769
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1248+1230A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257769 | ||||||
| chr13:28257775
|
A | T | 3 | a0001c0001t0002g0191a0001c0001t0020g0190a0001c0001t0020g0192 | 3 | NA18991.hp1 NA19003.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1248+1236A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257775 | ||||||
| chr13:28257783
|
T | A | 2 | a0001c0001t0005g0182a0001c0001t0007g0183 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1248+1244T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257783 | ||||||
| chr13:28257794
|
A | T | 2 | a0001c0001t0005g0182a0001c0001t0007g0183 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1248+1255A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257794 | ||||||
| chr13:28257795
|
T | A | 2 | a0001c0001t0005g0182a0001c0001t0007g0183 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1248+1256T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257795 | ||||||
| chr13:28257824
|
A | G | 6 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+1285A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257824 | ||||||
| chr13:28257851
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1248+1312C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257851 | ||||||
| chr13:28257935
|
C | G | 96 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(93): Show | 96 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(93): Show |
intron_variant | MODIFIER | c.1248+1396C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28257935 | ||||||
| chr13:28258085
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1248+1546C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258085 | ||||||
| chr13:28258145
|
C | T | 2 | a0001c0001t0011g0184a0001c0001t0019g0185 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1248+1606C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258145 | ||||||
| chr13:28258169
|
A | G | 2 | a0001c0001t0023g0171a0001c0001t0024g0226 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1248+1630A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258169 | ||||||
| chr13:28258239
|
G | C | 93 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(90): Show | 93 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(90): Show |
intron_variant | MODIFIER | c.1248+1700G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258239 | ||||||
| chr13:28258397
|
A | G | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1248+1858A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258397 | ||||||
| chr13:28258662
|
C | T | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1249-1785C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258662 | ||||||
| chr13:28258850
|
A | G | 74 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(71): Show | 74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.1249-1597A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28258850 | ||||||
| chr13:28259006
|
C | T | 74 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(71): Show | 74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.1249-1441C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259006 | ||||||
| chr13:28259047
|
A | G | 1 | a0001c0001t0046g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1249-1400A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259047 | ||||||
| chr13:28259064
|
C | T | 1 | a0001c0001t0004g0109 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1249-1383C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259064 | ||||||
| chr13:28259131
|
A | AT | 43 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(40): Show | 43 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1249-1302dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28259131 | |||||
| chr13:28259131
|
A | ATT | 5 | a0001c0002t0012g0162a0001c0002t0012g0209a0001c0002t0012g0211others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-1303_1249-130 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28259131 | |||||
| chr13:28259135
|
T | C | 74 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(71): Show | 74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.1249-1312T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259135 | ||||||
| chr13:28259166
|
C | G | 2 | a0001c0001t0005g0179a0001c0001t0007g0178 | 2 | HG01433.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1249-1281C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259166 | ||||||
| chr13:28259173
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1249-1274G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259173 | ||||||
| chr13:28259235
|
C | G | 64 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0022others(61): Show | 64 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(61): Show |
intron_variant | MODIFIER | c.1249-1212C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259235 | ||||||
| chr13:28259273
|
G | A | 1 | a0001c0001t0005g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1249-1174G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259273 | ||||||
| chr13:28259300
|
G | GT | 5 | a0001c0001t0013g0015a0001c0001t0013g0127a0001c0001t0013g0128others(2): Show | 5 | HG00099.hp2 HG03225.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-1139dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr13 | 28259300 | |||||
| chr13:28259301
|
T | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1249-1146T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259301 | ||||||
| chr13:28259307
|
T | C | 2 | a0001c0001t0002g0195a0001c0001t0035g0199 | 2 | NA18974.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1249-1140T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259307 | ||||||
| chr13:28259430
|
C | G | 1 | a0001c0001t0004g0109 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1249-1017C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259430 | ||||||
| chr13:28259482
|
T | C | 4 | a0001c0001t0011g0187a0001c0001t0011g0242a0001c0001t0019g0238others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-965T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259482 | ||||||
| chr13:28259641
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1249-806A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259641 | ||||||
| chr13:28259799
|
C | T | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-648C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259799 | ||||||
| chr13:28259879
|
C | T | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-568C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259879 | ||||||
| chr13:28259955
|
A | G | 2 | a0001c0001t0005g0206a0001c0001t0030g0161 | 2 | HG00639.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1249-492A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28259955 | ||||||
| chr13:28260119
|
G | A | 11 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(8): Show | 11 | HG01496.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1249-328G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28260119 | ||||||
| chr13:28260227
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1249-220T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 7/18 | chr13 | 28260227 | ||||||
| chr13:28260648
|
T | C | 1 | a0001c0001t0013g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1353+97T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28260648 | ||||||
| chr13:28260717
|
CT | C | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1353+170delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr13 | 28260717 | |||||
| chr13:28260723
|
A | G | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1353+172A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28260723 | ||||||
| chr13:28260797
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1353+246T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28260797 | ||||||
| chr13:28260988
|
G | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1354-413G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28260988 | ||||||
| chr13:28261165
|
C | T | 70 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(67): Show | 70 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1354-236C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261165 | ||||||
| chr13:28261230
|
C | T | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1354-171C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261230 | ||||||
| chr13:28261268
|
A | C | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1354-133A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261268 | ||||||
| chr13:28261325
|
G | A | 93 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(90): Show | 93 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(90): Show |
intron_variant | MODIFIER | c.1354-76G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261325 | ||||||
| chr13:28261339
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1354-62A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261339 | ||||||
| chr13:28261390
|
T | TC | 248 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.1354-11_1354-10ins others(1): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 8/18 | chr13 | 28261390 | ||||||
| chr13:28261510
|
C | T | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1411+52C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28261510 | ||||||
| chr13:28261511
|
G | T | 1 | a0001c0001t0005g0182 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1411+53G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28261511 | ||||||
| chr13:28261546
|
T | C | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1411+88T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28261546 | ||||||
| chr13:28261832
|
C | CA | 140 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.1411+393dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28261832 | |||||
| chr13:28261832
|
C | CAA | 8 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0096others(5): Show | 8 | HG01433.hp1 HG02083.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1411+392_1411+393d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28261832 | |||||
| chr13:28261849
|
AAAG | A | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1411+392_1411+394d others(5): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28261849 | ||||||
| chr13:28262068
|
G | A | 4 | a0001c0001t0005g0179a0001c0001t0005g0206a0001c0001t0007g0178others(1): Show | 4 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411+610G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262068 | ||||||
| chr13:28262070
|
C | A | 70 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(67): Show | 70 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1411+612C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262070 | ||||||
| chr13:28262136
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0157 | 2 | NA18961.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1411+678T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262136 | ||||||
| chr13:28262180
|
A | G | 1 | a0001c0001t0006g0133 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1411+722A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262180 | ||||||
| chr13:28262194
|
A | T | 3 | a0001c0001t0002g0191a0001c0001t0020g0190a0001c0001t0020g0192 | 3 | NA18991.hp1 NA19003.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1411+736A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262194 | ||||||
| chr13:28262239
|
T | A | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1411+781T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262239 | ||||||
| chr13:28262255
|
C | G | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1411+797C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262255 | ||||||
| chr13:28262422
|
G | A | 69 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(66): Show | 69 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.1411+964G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28262422 | ||||||
| chr13:28262713
|
CA | C | 106 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(103): Show | 106 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(103): Show |
intron_variant | MODIFIER | c.1411+1258delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28262713 | |||||
| chr13:28263090
|
G | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1411+1632G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263090 | ||||||
| chr13:28263103
|
A | G | 1 | a0001c0001t0023g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1411+1645A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263103 | ||||||
| chr13:28263159
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0004g0090 | 2 | HG02004.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1411+1701G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263159 | ||||||
| chr13:28263334
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1411+1876A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263334 | ||||||
| chr13:28263835
|
G | A | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1411+2377G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263835 | ||||||
| chr13:28263853
|
A | AT | 6 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411+2402dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28263853 | |||||
| chr13:28263903
|
C | G | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1411+2445C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263903 | ||||||
| chr13:28263951
|
G | A | 3 | a0001c0001t0008g0245a0001c0001t0008g0246a0001c0001t0008g0247 | 3 | HG01496.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1411+2493G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263951 | ||||||
| chr13:28263970
|
C | T | 2 | a0001c0001t0006g0030a0001c0001t0045g0102 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1411+2512C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28263970 | ||||||
| chr13:28264033
|
T | G | 2 | a0001c0001t0031g0223a0001c0001t0047g0019 | 2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1411+2575T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264033 | ||||||
| chr13:28264173
|
ATAAT | A | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412-2539_1412-253 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28264173 | |||||
| chr13:28264289
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1412-2426A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264289 | ||||||
| chr13:28264355
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1412-2360A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264355 | ||||||
| chr13:28264391
|
T | G | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1412-2324T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264391 | ||||||
| chr13:28264499
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1412-2216G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264499 | ||||||
| chr13:28264658
|
C | G | 2 | a0001c0001t0002g0038a0001c0001t0002g0039 | 2 | HG02040.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1412-2057C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264658 | ||||||
| chr13:28264771
|
G | C | 31 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(28): Show | 31 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1412-1944G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264771 | ||||||
| chr13:28264835
|
G | T | 1 | a0001c0001t0005g0175 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1412-1880G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264835 | ||||||
| chr13:28264931
|
T | C | 1 | a0001c0001t0009g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1412-1784T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264931 | ||||||
| chr13:28264940
|
C | T | 1 | a0001c0001t0009g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1412-1775C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28264940 | ||||||
| chr13:28265012
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1412-1703G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28265012 | ||||||
| chr13:28265065
|
C | T | 1 | a0001c0007t0021g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1412-1650C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28265065 | ||||||
| chr13:28265174
|
G | A | 2 | a0001c0001t0006g0016a0001c0001t0006g0017 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1412-1541G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28265174 | ||||||
| chr13:28265189
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1412-1526A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28265189 | ||||||
| chr13:28265719
|
GT | G | 11 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(8): Show | 11 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-971delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28265719 | |||||
| chr13:28265719
|
GTTTTTTT others(317): Show |
G | 11 | a0001c0001t0001g0129a0001c0001t0004g0059a0001c0001t0009g0160others(8): Show | 11 | HG01109.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412-984_1412-661d others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28265719 | |||||
| chr13:28265719
|
GTTTTTTT others(318): Show |
G | 156 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1412-985_1412-661d others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28265719 | |||||
| chr13:28265719
|
GTTTTTTT others(319): Show |
G | 67 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(64): Show | 67 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.1412-986_1412-661d others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28265719 | |||||
| chr13:28266036
|
GT | G | 13 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0006g0013others(10): Show | 13 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-661delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr13 | 28266036 | |||||
| chr13:28266084
|
G | A | 7 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0075others(4): Show | 7 | NA18944.hp1 NA18981.hp1 NA19074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412-631G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 9/18 | chr13 | 28266084 | ||||||
| chr13:28267042
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1574-53A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 10/18 | chr13 | 28267042 | ||||||
| chr13:28267262
|
C | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1691-38C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 11/18 | chr13 | 28267262 | ||||||
| chr13:28267492
|
C | T | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792+91C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267492 | ||||||
| chr13:28267551
|
C | T | 2 | a0001c0001t0005g0208a0001c0001t0007g0237 | 2 | NA18946.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1792+150C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267551 | ||||||
| chr13:28267628
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1792+227G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267628 | ||||||
| chr13:28267703
|
A | G | 1 | a0001c0001t0004g0109 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1792+302A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267703 | ||||||
| chr13:28267876
|
G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1792+475G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267876 | ||||||
| chr13:28267925
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+524G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267925 | ||||||
| chr13:28267927
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+526T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267927 | ||||||
| chr13:28267928
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+527G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267928 | ||||||
| chr13:28267932
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+531G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267932 | ||||||
| chr13:28267935
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+534A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267935 | ||||||
| chr13:28267936
|
A | C | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+535A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267936 | ||||||
| chr13:28267938
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+537A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267938 | ||||||
| chr13:28267939
|
A | T | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+538A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267939 | ||||||
| chr13:28267940
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1792+539G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28267940 | ||||||
| chr13:28268171
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1792+770C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28268171 | ||||||
| chr13:28268319
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+918A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28268319 | ||||||
| chr13:28268485
|
G | T | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1792+1084G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28268485 | ||||||
| chr13:28268703
|
A | G | 1 | a0001c0001t0005g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1792+1302A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28268703 | ||||||
| chr13:28268782
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792+1381A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28268782 | ||||||
| chr13:28268813
|
CT | C | 4 | a0001c0001t0001g0093a0001c0001t0015g0250a0001c0001t0029g0249others(1): Show | 4 | HG03098.hp1 HG03516.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792+1421delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr13 | 28268813 | |||||
| chr13:28269284
|
A | C | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1793-1417A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269284 | ||||||
| chr13:28269385
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1793-1316C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269385 | ||||||
| chr13:28269626
|
CTT | C | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1793-1074_1793-107 others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269626 | ||||||
| chr13:28269674
|
C | T | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1793-1027C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269674 | ||||||
| chr13:28269702
|
T | C | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1793-999T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269702 | ||||||
| chr13:28269711
|
G | A | 3 | a0001c0003t0001g0136a0001c0003t0004g0135a0001c0003t0014g0078 | 3 | HG02922.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1793-990G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269711 | ||||||
| chr13:28269776
|
T | C | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1793-925T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28269776 | ||||||
| chr13:28270019
|
G | T | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1793-682G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270019 | ||||||
| chr13:28270024
|
T | C | 71 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(68): Show | 71 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1793-677T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270024 | ||||||
| chr13:28270068
|
A | G | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0014g0111others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1793-633A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270068 | ||||||
| chr13:28270258
|
A | G | 8 | a0001c0001t0002g0115a0001c0001t0002g0164a0001c0001t0002g0169others(5): Show | 8 | HG02071.hp1 HG02523.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1793-443A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270258 | ||||||
| chr13:28270571
|
A | G | 1 | a0001c0001t0005g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1793-130A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270571 | ||||||
| chr13:28270590
|
C | A | 4 | a0001c0001t0017g0204a0001c0001t0017g0205a0001c0001t0023g0171others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793-111C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270590 | ||||||
| chr13:28270674
|
C | A | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1793-27C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 12/18 | chr13 | 28270674 | ||||||
| chr13:28270910
|
C | T | 1 | a0001c0001t0022g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1958+44C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28270910 | ||||||
| chr13:28271054
|
T | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958+188T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271054 | ||||||
| chr13:28271074
|
G | A | 11 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(8): Show | 11 | HG01496.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1958+208G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271074 | ||||||
| chr13:28271074
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1958+208G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271074 | ||||||
| chr13:28271129
|
A | G | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1958+263A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271129 | ||||||
| chr13:28271261
|
A | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1958+395A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271261 | ||||||
| chr13:28271448
|
T | A | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1959-533T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271448 | ||||||
| chr13:28271461
|
A | T | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1959-520A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271461 | ||||||
| chr13:28271574
|
C | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1959-407C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271574 | ||||||
| chr13:28271591
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1959-390A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271591 | ||||||
| chr13:28271784
|
A | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1959-197A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271784 | ||||||
| chr13:28271848
|
G | A | 1 | a0001c0001t0046g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1959-133G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271848 | ||||||
| chr13:28271855
|
A | G | 1 | a0001c0001t0002g0149 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1959-126A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271855 | ||||||
| chr13:28271934
|
T | A | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1959-47T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 13/18 | chr13 | 28271934 | ||||||
| chr13:28272270
|
T | C | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2049+199T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28272270 | ||||||
| chr13:28272381
|
C | T | 2 | a0001c0001t0010g0121a0001c0001t0010g0122 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2049+310C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28272381 | ||||||
| chr13:28272572
|
C | CT | 6 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2049+515dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr13 | 28272572 | |||||
| chr13:28272998
|
C | T | 61 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0022others(58): Show | 61 | HG01081.hp1 HG01099.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.2049+927C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28272998 | ||||||
| chr13:28273275
|
C | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2049+1204C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273275 | ||||||
| chr13:28273342
|
C | T | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2049+1271C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273342 | ||||||
| chr13:28273377
|
A | G | 131 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(128): Show | 131 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.2049+1306A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273377 | ||||||
| chr13:28273505
|
G | A | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2049+1434G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273505 | ||||||
| chr13:28273555
|
C | T | 2 | a0001c0001t0001g0105a0001c0009t0001g0063 | 2 | HG02056.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2049+1484C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273555 | ||||||
| chr13:28273600
|
C | CA | 11 | a0001c0001t0005g0208a0001c0001t0007g0237a0001c0001t0010g0121others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.2049+1541dupA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr13 | 28273600 | |||||
| chr13:28273801
|
G | A | 1 | a0001c0001t0009g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2049+1730G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273801 | ||||||
| chr13:28273859
|
T | C | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2049+1788T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28273859 | ||||||
| chr13:28274256
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2049+2185C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274256 | ||||||
| chr13:28274332
|
G | C | 1 | a0001c0001t0007g0237 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2049+2261G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274332 | ||||||
| chr13:28274522
|
C | T | 10 | a0001c0001t0002g0191a0001c0001t0002g0200a0001c0001t0002g0202others(7): Show | 10 | HG02080.hp1 HG02135.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.2049+2451C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274522 | ||||||
| chr13:28274578
|
C | G | 72 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(69): Show | 72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.2049+2507C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274578 | ||||||
| chr13:28274627
|
C | T | 2 | a0001c0001t0011g0184a0001c0001t0019g0185 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2049+2556C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274627 | ||||||
| chr13:28274742
|
A | G | 1 | a0001c0001t0030g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2050-2495A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28274742 | ||||||
| chr13:28275208
|
C | G | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2050-2029C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275208 | ||||||
| chr13:28275539
|
A | G | 11 | a0001c0001t0011g0184a0001c0001t0011g0187a0001c0001t0011g0242others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2050-1698A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275539 | ||||||
| chr13:28275625
|
G | A | 1 | a0001c0001t0056g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2050-1612G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275625 | ||||||
| chr13:28275784
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0003g0001a0001c0001t0003g0003others(1): Show | 4 | HG02622.hp1 HG02895.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050-1453A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275784 | ||||||
| chr13:28275832
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0094 | 2 | HG01167.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2050-1405T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275832 | ||||||
| chr13:28275979
|
TA | T | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.2050-1257delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28275979 | ||||||
| chr13:28276073
|
C | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2050-1164C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28276073 | ||||||
| chr13:28276430
|
A | G | 72 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(69): Show | 72 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.2050-807A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28276430 | ||||||
| chr13:28276575
|
G | A | 1 | a0001c0001t0004g0051 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2050-662G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28276575 | ||||||
| chr13:28276699
|
C | T | 1 | a0001c0001t0043g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2050-538C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28276699 | ||||||
| chr13:28277120
|
G | A | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2050-117G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28277120 | ||||||
| chr13:28277150
|
C | T | 1 | a0001c0004t0004g0064 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2050-87C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28277150 | ||||||
| chr13:28277195
|
G | A | 127 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(124): Show | 127 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.2050-42G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 14/18 | chr13 | 28277195 | ||||||
| chr13:28277585
|
G | A | 105 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(102): Show | 105 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.2189+209G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28277585 | ||||||
| chr13:28277680
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2189+304A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28277680 | ||||||
| chr13:28277709
|
C | T | 14 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(11): Show | 14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.2189+333C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28277709 | ||||||
| chr13:28277716
|
A | G | 74 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(71): Show | 74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.2189+340A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28277716 | ||||||
| chr13:28278119
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2189+743T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278119 | ||||||
| chr13:28278435
|
A | G | 1 | a0001c0001t0015g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2189+1059A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278435 | ||||||
| chr13:28278636
|
A | T | 1 | a0001c0001t0002g0149 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2189+1260A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278636 | ||||||
| chr13:28278639
|
T | A | 1 | a0001c0001t0002g0149 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2189+1263T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278639 | ||||||
| chr13:28278644
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0101a0001c0001t0001g0134 | 3 | HG02523.hp2 NA18747.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2189+1268C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278644 | ||||||
| chr13:28278794
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2189+1418G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28278794 | ||||||
| chr13:28279094
|
A | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2190-1318A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28279094 | ||||||
| chr13:28279572
|
A | T | 74 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(71): Show | 74 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(71): Show |
intron_variant | MODIFIER | c.2190-840A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28279572 | ||||||
| chr13:28279858
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2190-554G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28279858 | ||||||
| chr13:28279941
|
A | C | 1 | a0001c0001t0004g0092 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2190-471A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28279941 | ||||||
| chr13:28279994
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2190-418T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28279994 | ||||||
| chr13:28280010
|
G | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026 | 3 | HG02886.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2190-402G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 15/18 | chr13 | 28280010 | ||||||
| chr13:28280555
|
A | AT | 123 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0022others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.2319+38dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 28280555 | |||||
| chr13:28280555
|
A | ATT | 32 | a0001c0001t0001g0021a0001c0001t0001g0061a0001c0001t0001g0094others(29): Show | 32 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.2319+37_2319+38dup others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 28280555 | |||||
| chr13:28280555
|
A | ATTT | 6 | a0001c0001t0005g0182a0001c0001t0007g0116a0001c0001t0007g0183others(3): Show | 6 | HG03098.hp2 HG03225.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.2319+36_2319+38dup others(3): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 28280555 | |||||
| chr13:28280555
|
A | T | 1 | a0001c0001t0027g0150 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2319+14A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | chr13 | 28280555 | ||||||
| chr13:28280555
|
AT | A | 14 | a0001c0001t0002g0010a0001c0001t0002g0036a0001c0001t0002g0037others(11): Show | 14 | HG02040.hp1 HG02083.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.2319+38delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr13 | 28280555 | |||||
| chr13:28280884
|
T | C | 1 | a0001c0001t0008g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2319+343T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | chr13 | 28280884 | ||||||
| chr13:28280948
|
G | A | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2320-367G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 16/18 | chr13 | 28280948 | ||||||
| chr13:28281466
|
A | G | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384+87A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281466 | ||||||
| chr13:28281469
|
AAG | A | 19 | a0001c0001t0001g0047a0001c0001t0001g0072a0001c0001t0001g0073others(16): Show | 19 | HG00438.hp1 HG01109.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.2384+94_2384+95del others(2): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28281469 | |||||
| chr13:28281648
|
A | G | 1 | a0001c0001t0005g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2384+269A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281648 | ||||||
| chr13:28281662
|
A | G | 1 | a0001c0001t0034g0193 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2384+283A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281662 | ||||||
| chr13:28281723
|
A | G | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2384+344A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281723 | ||||||
| chr13:28281760
|
A | C | 1 | a0001c0001t0006g0133 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2384+381A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281760 | ||||||
| chr13:28281766
|
CT | C | 156 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(153): Show | 156 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.2384+407delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28281766 | |||||
| chr13:28281766
|
CTT | C | 71 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0213others(68): Show | 71 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.2384+406_2384+407d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28281766 | |||||
| chr13:28281810
|
C | T | 1 | a0001c0001t0038g0243 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2384+431C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281810 | ||||||
| chr13:28281820
|
G | T | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384+441G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281820 | ||||||
| chr13:28281918
|
G | A | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384+539G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28281918 | ||||||
| chr13:28282012
|
G | T | 4 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0008others(1): Show | 4 | HG02083.hp1 NA18979.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2384+633G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282012 | ||||||
| chr13:28282056
|
A | G | 1 | a0001c0001t0006g0030 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2384+677A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282056 | ||||||
| chr13:28282068
|
G | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2384+689G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282068 | ||||||
| chr13:28282233
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384+854A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282233 | ||||||
| chr13:28282339
|
T | TG | 6 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384+961dupG | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28282339 | |||||
| chr13:28282340
|
G | GT | 118 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0094others(115): Show | 118 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.2384+973dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28282340 | |||||
| chr13:28282340
|
G | GTT | 8 | a0001c0001t0003g0231a0001c0001t0010g0121a0001c0001t0010g0122others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384+972_2384+973d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28282340 | |||||
| chr13:28282356
|
A | G | 73 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(70): Show | 73 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.2384+977A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282356 | ||||||
| chr13:28282409
|
C | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2384+1030C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282409 | ||||||
| chr13:28282777
|
C | T | 14 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(11): Show | 14 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.2384+1398C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282777 | ||||||
| chr13:28282880
|
G | GTTTA | 88 | a0001c0001t0001g0047a0001c0001t0001g0072a0001c0001t0001g0073others(85): Show | 88 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(85): Show |
intron_variant | MODIFIER | c.2384+1525_2384+152 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28282880 | |||||
| chr13:28282880
|
G | GTTTATTT others(1): Show |
6 | a0001c0001t0001g0084a0001c0001t0001g0138a0001c0001t0001g0156others(3): Show | 6 | HG00438.hp1 NA18941.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.2384+1521_2384+152 others(12): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28282880 | |||||
| chr13:28282920
|
G | A | 12 | a0001c0001t0002g0191a0001c0001t0002g0197a0001c0001t0002g0200others(9): Show | 12 | HG02080.hp1 HG02135.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.2384+1541G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282920 | ||||||
| chr13:28282942
|
A | G | 15 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(12): Show | 15 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.2384+1563A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28282942 | ||||||
| chr13:28283030
|
C | G | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2384+1651C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283030 | ||||||
| chr13:28283073
|
G | A | 84 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(81): Show | 84 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.2384+1694G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283073 | ||||||
| chr13:28283085
|
A | G | 103 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(100): Show | 103 | HG00099.hp2 HG00438.hp1 HG01081.hp1 others(100): Show |
intron_variant | MODIFIER | c.2384+1706A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283085 | ||||||
| chr13:28283105
|
A | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2384+1726A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283105 | ||||||
| chr13:28283127
|
C | T | 15 | a0001c0001t0005g0117a0001c0001t0005g0176a0001c0001t0005g0179others(12): Show | 15 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.2384+1748C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283127 | ||||||
| chr13:28283241
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2384+1862G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283241 | ||||||
| chr13:28283306
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2384+1927T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283306 | ||||||
| chr13:28283326
|
G | A | 2 | a0001c0001t0017g0204a0001c0001t0017g0205 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2384+1947G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283326 | ||||||
| chr13:28283378
|
T | A | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2384+1999T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283378 | ||||||
| chr13:28283450
|
A | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2384+2071A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283450 | ||||||
| chr13:28283468
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2384+2089A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283468 | ||||||
| chr13:28283552
|
A | T | 94 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(91): Show | 94 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.2384+2173A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283552 | ||||||
| chr13:28283571
|
A | G | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2384+2192A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283571 | ||||||
| chr13:28283629
|
C | G | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2384+2250C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283629 | ||||||
| chr13:28283641
|
A | G | 9 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.2384+2262A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283641 | ||||||
| chr13:28283737
|
T | C | 11 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(8): Show | 11 | HG01496.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2384+2358T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283737 | ||||||
| chr13:28283796
|
G | A | 8 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(5): Show | 8 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2384+2417G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28283796 | ||||||
| chr13:28284061
|
G | A | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2384+2682G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284061 | ||||||
| chr13:28284155
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2384+2776T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284155 | ||||||
| chr13:28284381
|
A | AT | 19 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0054others(16): Show | 19 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2384+3018dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28284381 | |||||
| chr13:28284381
|
AT | A | 13 | a0001c0001t0001g0058a0001c0001t0011g0187a0001c0001t0011g0242others(10): Show | 13 | HG01109.hp1 HG02572.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.2384+3018delT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr13 | 28284381 | |||||
| chr13:28284531
|
G | T | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2384+3152G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284531 | ||||||
| chr13:28284664
|
T | A | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2384+3285T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284664 | ||||||
| chr13:28284675
|
C | T | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2384+3296C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284675 | ||||||
| chr13:28284877
|
A | G | 1 | a0001c0001t0026g0239 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2385-3107A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28284877 | ||||||
| chr13:28285434
|
T | C | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2385-2550T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28285434 | ||||||
| chr13:28285662
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2385-2322A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28285662 | ||||||
| chr13:28286237
|
A | G | 1 | a0001c0001t0005g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2385-1747A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28286237 | ||||||
| chr13:28286601
|
G | A | 2 | a0001c0001t0005g0182a0001c0001t0007g0183 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2385-1383G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28286601 | ||||||
| chr13:28286778
|
A | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2385-1206A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28286778 | ||||||
| chr13:28287004
|
C | T | 70 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(67): Show | 70 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.2385-980C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287004 | ||||||
| chr13:28287054
|
G | A | 9 | a0001c0001t0001g0054a0001c0001t0004g0051a0001c0001t0010g0121others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.2385-930G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287054 | ||||||
| chr13:28287127
|
A | G | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2385-857A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287127 | ||||||
| chr13:28287253
|
T | C | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2385-731T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287253 | ||||||
| chr13:28287369
|
G | A | 32 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(29): Show | 32 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2385-615G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287369 | ||||||
| chr13:28287478
|
C | T | 1 | a0001c0001t0042g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2385-506C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287478 | ||||||
| chr13:28287533
|
A | G | 1 | a0001c0001t0005g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2385-451A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287533 | ||||||
| chr13:28287565
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2385-419C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287565 | ||||||
| chr13:28287698
|
T | C | 248 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.2385-286T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287698 | ||||||
| chr13:28287929
|
A | G | 96 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(93): Show | 96 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(93): Show |
intron_variant | MODIFIER | c.2385-55A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 17/18 | chr13 | 28287929 | ||||||
| chr13:28288492
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0004g0057 | 2 | HG01081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2523+370A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288492 | ||||||
| chr13:28288665
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2523+543C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288665 | ||||||
| chr13:28288752
|
T | A | 6 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0175others(3): Show | 6 | HG00639.hp2 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2523+630T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288752 | ||||||
| chr13:28288828
|
A | AT | 102 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0028others(99): Show | 102 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.2523+726dupT | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28288828 | |||||
| chr13:28288828
|
A | ATT | 9 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(6): Show | 9 | HG01167.hp2 HG02071.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.2523+725_2523+726d others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28288828 | |||||
| chr13:28288858
|
T | TCTCA | 142 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.2523+739_2523+740i others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28288858 | |||||
| chr13:28288858
|
T | TCTCG | 94 | a0001c0001t0001g0213a0001c0001t0002g0002a0001c0001t0002g0010others(91): Show | 94 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.2523+739_2523+740i others(6): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28288858 | |||||
| chr13:28288879
|
T | C | 14 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2523+757T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288879 | ||||||
| chr13:28288895
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2523+773A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288895 | ||||||
| chr13:28288902
|
C | T | 1 | a0001c0001t0007g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2523+780C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288902 | ||||||
| chr13:28288919
|
C | T | 21 | a0001c0001t0005g0117a0001c0001t0005g0172a0001c0001t0005g0173others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.2523+797C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28288919 | ||||||
| chr13:28289007
|
T | C | 1 | a0001c0001t0031g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2523+885T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289007 | ||||||
| chr13:28289061
|
C | T | 45 | a0001c0001t0002g0012a0001c0001t0002g0036a0001c0001t0002g0037others(42): Show | 45 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2523+939C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289061 | ||||||
| chr13:28289106
|
A | G | 2 | a0001c0001t0032g0225a0001c0001t0043g0252 | 2 | HG02602.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2523+984A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289106 | ||||||
| chr13:28289178
|
A | G | 8 | a0001c0001t0001g0047a0001c0001t0001g0072a0001c0001t0001g0073others(5): Show | 8 | HG02080.hp2 HG02523.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.2523+1056A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289178 | ||||||
| chr13:28289200
|
G | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2523+1078G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289200 | ||||||
| chr13:28289467
|
G | A | 6 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0188others(3): Show | 6 | HG00639.hp2 HG01099.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2523+1345G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289467 | ||||||
| chr13:28289610
|
A | G | 8 | a0001c0001t0002g0233a0001c0001t0002g0240a0001c0001t0003g0229others(5): Show | 8 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2523+1488A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289610 | ||||||
| chr13:28289613
|
A | G | 9 | a0001c0001t0002g0233a0001c0001t0002g0240a0001c0001t0003g0229others(6): Show | 9 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2523+1491A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289613 | ||||||
| chr13:28289618
|
G | A | 8 | a0001c0001t0002g0233a0001c0001t0002g0240a0001c0001t0003g0229others(5): Show | 8 | HG01891.hp2 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2523+1496G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289618 | ||||||
| chr13:28289632
|
A | T | 5 | a0001c0001t0008g0244a0001c0001t0008g0245a0001c0001t0008g0246others(2): Show | 5 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2523+1510A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289632 | ||||||
| chr13:28289638
|
T | G | 2 | a0001c0001t0011g0184a0001c0001t0019g0185 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2523+1516T>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289638 | ||||||
| chr13:28289648
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2523+1526A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289648 | ||||||
| chr13:28289649
|
C | A | 1 | a0001c0001t0003g0214 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2523+1527C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289649 | ||||||
| chr13:28289653
|
G | A | 1 | a0001c0001t0006g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2523+1531G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289653 | ||||||
| chr13:28289698
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2523+1576G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289698 | ||||||
| chr13:28289739
|
G | A | 7 | a0001c0001t0003g0009a0001c0001t0010g0121a0001c0001t0010g0122others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2523+1617G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289739 | ||||||
| chr13:28289879
|
C | G | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2523+1757C>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289879 | ||||||
| chr13:28289897
|
A | G | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2523+1775A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28289897 | ||||||
| chr13:28290063
|
C | T | 5 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(2): Show | 5 | HG01891.hp2 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2523+1941C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290063 | ||||||
| chr13:28290095
|
G | A | 1 | a0001c0001t0032g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2523+1973G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290095 | ||||||
| chr13:28290112
|
A | G | 1 | a0001c0001t0009g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2523+1990A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290112 | ||||||
| chr13:28290235
|
A | T | 6 | a0001c0001t0008g0007a0001c0001t0008g0244a0001c0001t0008g0245others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2523+2113A>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290235 | ||||||
| chr13:28290405
|
G | C | 1 | a0001c0001t0007g0116 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2524-1977G>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290405 | ||||||
| chr13:28290414
|
T | C | 2 | a0001c0001t0013g0015a0001c0001t0046g0035 | 2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2524-1968T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290414 | ||||||
| chr13:28290485
|
C | T | 7 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2524-1897C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290485 | ||||||
| chr13:28290511
|
A | G | 128 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(125): Show | 128 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.2524-1871A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290511 | ||||||
| chr13:28290614
|
A | G | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | NA19078.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2524-1768A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290614 | ||||||
| chr13:28290713
|
A | G | 1 | a0001c0001t0047g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2524-1669A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28290713 | ||||||
| chr13:28290955
|
T | TATTC | 247 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.2524-1424_2524-142 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28290955 | |||||
| chr13:28291059
|
A | G | 1 | a0001c0001t0004g0092 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2524-1323A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291059 | ||||||
| chr13:28291205
|
ATGTT | A | 3 | a0001c0001t0001g0071a0001c0001t0004g0067a0001c0008t0001g0068 | 3 | HG01358.hp1 HG02004.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2524-1174_2524-117 others(8): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28291205 | |||||
| chr13:28291260
|
A | G | 80 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(77): Show | 80 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.2524-1122A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291260 | ||||||
| chr13:28291723
|
C | T | 2 | a0001c0001t0002g0195a0001c0001t0035g0199 | 2 | NA18974.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2524-659C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291723 | ||||||
| chr13:28291724
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0004g0057 | 2 | HG01081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2524-658G>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291724 | ||||||
| chr13:28291790
|
C | T | 69 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0012others(66): Show | 69 | HG00438.hp2 HG00597.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.2524-592C>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291790 | ||||||
| chr13:28291858
|
T | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2524-524T>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291858 | ||||||
| chr13:28291987
|
T | C | 14 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0052others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2524-395T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28291987 | ||||||
| chr13:28292080
|
C | A | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2524-302C>A | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28292080 | ||||||
| chr13:28292127
|
G | T | 248 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.2524-255G>T | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28292127 | ||||||
| chr13:28292159
|
A | G | 143 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.2524-223A>G | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28292159 | ||||||
| chr13:28292207
|
A | C | 1 | a0001c0001t0024g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2524-175A>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28292207 | ||||||
| chr13:28292283
|
CA | C | 10 | a0001c0001t0006g0013a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2524-91delA | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28292283 | |||||
| chr13:28292310
|
T | C | 3 | a0001c0001t0015g0250a0001c0001t0029g0249a0003c0006t0015g0251 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2524-72T>C | PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | chr13 | 28292310 | ||||||
| chr13:28292323
|
GTAGA | G | 8 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0124others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.2524-56_2524-53del others(4): Show |
PAN3 | ENSG00000152520.14 | transcript | ENST00000380958.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr13 | 28292323 |