Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 144347 |
| ensemblid | ENSG00000178882.15 |
| hgncid | 27051 |
| symbol | RFLNA |
| name | refilin A |
| refseq_nuc | NM_001365156.1 |
| refseq_prot | NP_001352085.1 |
| ensembl_nuc | ENST00000546355.4 |
| ensembl_prot | ENSP00000444080.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 124295093 |
| end | 124316024 |
| strand | + |
| ver | v1.2 |
| region | chr12:124295093-124316024 |
| region5000 | chr12:124290093-124321024 |
| regionname0 | RFLNA_chr12_124295093_124316024 |
| regionname5000 | RFLNA_chr12_124290093_124321024 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 216 | 378 | 81 | 71 | 167 | 13 | 44 | 125 | RFLNA_chr12_124290093_124321024 | RFLNA | MVGHL others(211): Show |
chr12 | 124290093 | 124321024 |
| a0002 | 0/0 | 216 | 6 | 4 | 1 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | MVGHL others(211): Show |
chr12 | 124290093 | 124321024 |
| a0003 | 0/0 | 216 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | MVGHL others(211): Show |
chr12 | 124290093 | 124321024 |
| a0004 | 0/0 | 216 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | MVGHL others(211): Show |
chr12 | 124290093 | 124321024 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 648 | 211 | 26 | 48 | 92 | 12 | 31 | RFLNA_chr12_124290093_124321024 | RFLNA | ATGGT others(643): Show |
chr12 | 124290093 | 124321024 | ||
| a0001c0002 | 0/0 | 648 | 142 | 31 | 23 | 74 | 1 | 13 | RFLNA_chr12_124290093_124321024 | RFLNA | ATGGT others(643): Show |
chr12 | 124290093 | 124321024 | ||
| a0001c0003 | 0/0 | 648 | 17 | 17 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | ATGGT others(643): Show |
chr12 | 124290093 | 124321024 | ||
| a0001c0004 | 0/0 | 648 | 7 | 7 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | ATGGT others(643): Show |
chr12 | 124290093 | 124321024 | ||
| a0001c0007 | 0/0 | 648 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | ATGGT others(643): Show |
chr12 | 124290093 | 124321024 | ||
| a0002c0005 | 0/0 | 648 | 6 | 4 | 1 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | ATGGT others(643): Show |
chr12 | 124290093 | 124321024 | ||
| a0003c0006 | 0/0 | 648 | 3 | 3 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | ATGGT others(643): Show |
chr12 | 124290093 | 124321024 | ||
| a0004c0008 | 0/0 | 648 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | ATGGT others(643): Show |
chr12 | 124290093 | 124321024 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2487 | 104 | 4 | 27 | 54 | 9 | 9 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0002 | 0/0 | 2487 | 16 | 5 | 3 | 3 | 1 | 4 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0004 | 0/0 | 2487 | 3 | 1 | 0 | 1 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0005 | 0/0 | 2487 | 20 | 2 | 4 | 5 | 1 | 8 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0006 | 0/0 | 2487 | 21 | 6 | 2 | 12 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0008 | 0/0 | 2487 | 14 | 2 | 5 | 6 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0009 | 1/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0011 | 0/0 | 2487 | 7 | 0 | 0 | 5 | 0 | 2 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0012 | 0/0 | 2487 | 5 | 2 | 2 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0013 | 0/0 | 2487 | 5 | 2 | 0 | 1 | 0 | 2 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0015 | 0/0 | 2487 | 4 | 0 | 4 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0021 | 0/0 | 2487 | 2 | 2 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0024 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0025 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0026 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0028 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0029 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0032 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0033 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0034 | 0/0 | 2504 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2499): Show |
chr12 | 124290093 | 124321024 |
| a0001c0001t0037 | 0/0 | 2498 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2493): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0002 | 0/0 | 2487 | 31 | 7 | 4 | 19 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0003 | 0/0 | 2487 | 36 | 0 | 10 | 24 | 1 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0004 | 0/0 | 2487 | 32 | 7 | 6 | 16 | 0 | 3 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0007 | 0/0 | 2487 | 17 | 5 | 2 | 5 | 0 | 5 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0010 | 0/0 | 2487 | 7 | 0 | 0 | 4 | 0 | 3 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0016 | 0/0 | 2498 | 4 | 0 | 0 | 4 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2493): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0017 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0019 | 0/0 | 2467 | 3 | 3 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2462): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0020 | 0/0 | 2487 | 2 | 0 | 0 | 2 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0022 | 0/0 | 2487 | 2 | 1 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0023 | 0/0 | 2487 | 2 | 2 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0027 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0030 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0002t0031 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0003t0009 | 0/0 | 2487 | 11 | 11 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0003t0014 | 0/0 | 2487 | 5 | 5 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0003t0036 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0004t0002 | 0/0 | 2487 | 7 | 7 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0001c0007t0002 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0002c0005t0002 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0002c0005t0005 | 0/0 | 2487 | 5 | 4 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0003c0006t0018 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| a0004c0008t0035 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | GGAGA others(2482): Show |
chr12 | 124290093 | 124321024 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0353 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0004g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0008g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0009g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0011g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0011g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0011g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0011g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0012g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0012g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0012g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0012g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0012g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0013g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0013g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0013g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0013g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0015g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0015g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0015g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0015g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0021g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0021g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0024g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0025g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0026g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0028g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0029g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0032g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0033g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0034g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0001t0037g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0004g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0007g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0010g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0010g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0010g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0010g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0010g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0010g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0016g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0016g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0016g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0016g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0017g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0017g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0017g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0019g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0019g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0019g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0020g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0020g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0022g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0022g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0023g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0023g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0027g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0030g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0002t0031g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0009g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0009g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0014g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0014g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0014g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0014g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0003t0036g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0004t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0004t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0004t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0004t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0004t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0004t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0004t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0001c0007t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0002c0005t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0002c0005t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0002c0005t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0002c0005t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0002c0005t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0002c0005t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0003c0006t0018g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0003c0006t0018g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0003c0006t0018g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| a0004c0008t0035g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0281 | EUR | GBR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | GBR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00280 | hp1 | a0002 | c0005 | t0002 | g0023 | EUR | FIN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | FIN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | FIN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0219 | EUR | FIN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00408 | hp1 | a0001 | c0002 | t0004 | g0351 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00408 | hp2 | a0001 | c0002 | t0020 | g0255 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0142 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0274 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00544 | hp2 | a0001 | c0001 | t0037 | g0174 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00621 | hp1 | a0001 | c0002 | t0004 | g0319 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0237 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0178 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0215 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0114 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0249 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01070 | hp1 | a0001 | c0002 | t0007 | g0003 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0171 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01071 | hp1 | a0001 | c0002 | t0007 | g0003 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01074 | hp1 | a0001 | c0001 | t0012 | g0363 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01099 | hp1 | a0002 | c0005 | t0005 | g0062 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0129 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0112 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0258 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0352 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01243 | hp1 | a0001 | c0002 | t0022 | g0053 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0183 | AMR | PUR | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01255 | hp1 | a0001 | c0002 | t0004 | g0378 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0138 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01257 | hp1 | a0001 | c0001 | t0025 | g0280 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01257 | hp2 | a0001 | c0001 | t0015 | g0279 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0137 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01258 | hp2 | a0001 | c0001 | t0015 | g0278 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0116 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01433 | hp2 | a0001 | c0001 | t0015 | g0184 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0150 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0227 | AMR | CLM | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0368 | EUR | IBS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0367 | EUR | IBS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01891 | hp2 | a0003 | c0006 | t0018 | g0026 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01928 | hp1 | a0001 | c0001 | t0008 | g0115 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0096 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0364 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01934 | hp2 | a0001 | c0002 | t0004 | g0373 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0358 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0093 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0376 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01975 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0101 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0140 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG01981 | hp2 | a0001 | c0001 | t0012 | g0357 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0149 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02004 | hp2 | a0001 | c0001 | t0015 | g0337 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0179 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02055 | hp1 | a0003 | c0006 | t0018 | g0033 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0059 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0225 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02074 | hp2 | a0001 | c0002 | t0004 | g0264 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0349 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0235 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02129 | hp1 | a0001 | c0001 | t0011 | g0070 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0220 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02132 | hp2 | a0001 | c0001 | t0008 | g0147 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02135 | hp2 | a0001 | c0002 | t0004 | g0263 | EAS | KHV | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0163 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02145 | hp2 | a0001 | c0003 | t0009 | g0120 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0113 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | CDX | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | CDX | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02165 | hp1 | a0001 | c0002 | t0003 | g0223 | EAS | CDX | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CDX | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02257 | hp1 | a0003 | c0006 | t0018 | g0035 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02257 | hp2 | a0001 | c0004 | t0002 | g0047 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02258 | hp1 | a0002 | c0005 | t0005 | g0054 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0068 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0176 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02273 | hp2 | a0001 | c0002 | t0004 | g0375 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02280 | hp2 | a0001 | c0003 | t0009 | g0005 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0377 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0210 | AMR | PEL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02451 | hp1 | a0001 | c0002 | t0030 | g0011 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02451 | hp2 | a0001 | c0002 | t0019 | g0182 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02572 | hp2 | a0001 | c0003 | t0009 | g0121 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02602 | hp1 | a0001 | c0001 | t0013 | g0124 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02602 | hp2 | a0001 | c0002 | t0010 | g0145 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02615 | hp1 | a0001 | c0003 | t0014 | g0069 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02615 | hp2 | a0002 | c0005 | t0005 | g0065 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02622 | hp1 | a0001 | c0002 | t0007 | g0372 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02622 | hp2 | a0001 | c0003 | t0009 | g0122 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0187 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02647 | hp2 | a0001 | c0002 | t0017 | g0260 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0128 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02698 | hp2 | a0001 | c0002 | t0010 | g0177 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02717 | hp1 | a0001 | c0002 | t0023 | g0192 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02723 | hp1 | a0001 | c0002 | t0004 | g0188 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02723 | hp2 | a0001 | c0003 | t0014 | g0185 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0191 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0293 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02738 | hp1 | a0001 | c0002 | t0010 | g0136 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0125 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02809 | hp1 | a0001 | c0004 | t0002 | g0270 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02809 | hp2 | a0001 | c0002 | t0023 | g0193 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02818 | hp1 | a0001 | c0003 | t0014 | g0072 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0197 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02886 | hp2 | a0001 | c0002 | t0007 | g0025 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02897 | hp1 | a0001 | c0004 | t0002 | g0048 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02897 | hp2 | a0001 | c0003 | t0036 | g0133 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02965 | hp1 | a0001 | c0003 | t0009 | g0132 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0250 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0262 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02970 | hp2 | a0001 | c0003 | t0009 | g0006 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02976 | hp1 | a0001 | c0002 | t0017 | g0261 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02976 | hp2 | a0002 | c0005 | t0005 | g0066 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03017 | hp1 | a0001 | c0001 | t0008 | g0117 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0200 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03041 | hp1 | a0001 | c0001 | t0021 | g0060 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0203 | AFR | GWD | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03098 | hp1 | a0001 | c0003 | t0009 | g0194 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0275 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0155 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03139 | hp1 | a0002 | c0005 | t0005 | g0064 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03139 | hp2 | a0001 | c0003 | t0009 | g0164 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03195 | hp1 | a0001 | c0003 | t0009 | g0119 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03195 | hp2 | a0001 | c0002 | t0031 | g0371 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03209 | hp1 | a0001 | c0002 | t0027 | g0273 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03209 | hp2 | a0001 | c0003 | t0014 | g0168 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03225 | hp1 | a0001 | c0002 | t0019 | g0186 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03225 | hp2 | a0001 | c0002 | t0007 | g0012 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03239 | hp2 | a0001 | c0001 | t0032 | g0189 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03453 | hp1 | a0001 | c0003 | t0009 | g0005 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0139 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0159 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0161 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03491 | hp1 | a0001 | c0002 | t0007 | g0106 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03491 | hp2 | a0001 | c0001 | t0013 | g0126 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03492 | hp1 | a0001 | c0002 | t0007 | g0105 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0158 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03516 | hp1 | a0001 | c0003 | t0009 | g0006 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | ESN | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03579 | hp1 | a0001 | c0002 | t0017 | g0257 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03654 | hp1 | a0001 | c0001 | t0026 | g0344 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0233 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0218 | SAS | STU | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0013 | SAS | STU | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0050 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0362 | SAS | PJL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03831 | hp2 | a0001 | c0002 | t0007 | g0085 | SAS | BEB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03834 | hp2 | a0001 | c0002 | t0004 | g0265 | SAS | BEB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03942 | hp1 | a0001 | c0001 | t0011 | g0051 | SAS | BEB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | BEB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG04184 | hp2 | a0001 | c0001 | t0034 | g0160 | SAS | BEB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG04199 | hp1 | a0001 | c0002 | t0007 | g0201 | SAS | STU | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG04199 | hp2 | a0001 | c0002 | t0007 | g0088 | SAS | STU | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0190 | SAS | STU | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG04204 | hp2 | a0001 | c0002 | t0004 | g0154 | SAS | STU | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | STU | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | STU | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18522 | hp1 | a0001 | c0002 | t0019 | g0018 | AFR | YRI | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18522 | hp2 | a0001 | c0002 | t0022 | g0071 | AFR | YRI | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18612 | hp1 | a0001 | c0002 | t0004 | g0127 | EAS | CHB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18612 | hp2 | a0001 | c0001 | t0033 | g0032 | EAS | CHB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | CHB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | YRI | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0110 | AFR | YRI | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18939 | hp1 | a0001 | c0002 | t0007 | g0087 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0224 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18943 | hp1 | a0001 | c0002 | t0003 | g0212 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18946 | hp1 | a0001 | c0002 | t0007 | g0083 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18947 | hp2 | a0001 | c0001 | t0013 | g0090 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18948 | hp1 | a0001 | c0002 | t0020 | g0238 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18950 | hp1 | a0001 | c0002 | t0004 | g0295 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18951 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18952 | hp2 | a0001 | c0001 | t0008 | g0143 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18954 | hp1 | a0001 | c0002 | t0010 | g0180 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18960 | hp1 | a0001 | c0002 | t0007 | g0080 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18961 | hp1 | a0001 | c0001 | t0028 | g0204 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18966 | hp1 | a0001 | c0001 | t0008 | g0167 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18966 | hp2 | a0001 | c0001 | t0029 | g0146 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18968 | hp2 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0232 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18970 | hp1 | a0001 | c0002 | t0007 | g0099 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18974 | hp1 | a0001 | c0001 | t0008 | g0217 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18974 | hp2 | a0001 | c0002 | t0004 | g0329 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18977 | hp1 | a0001 | c0002 | t0004 | g0253 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18979 | hp2 | a0001 | c0002 | t0016 | g0135 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18980 | hp2 | a0001 | c0002 | t0004 | g0259 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18981 | hp2 | a0001 | c0002 | t0003 | g0236 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18982 | hp1 | a0001 | c0002 | t0004 | g0252 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0222 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18985 | hp1 | a0001 | c0002 | t0010 | g0370 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18985 | hp2 | a0001 | c0001 | t0006 | g0231 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18990 | hp1 | a0001 | c0001 | t0008 | g0134 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18993 | hp2 | a0001 | c0002 | t0016 | g0230 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0228 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18994 | hp2 | a0001 | c0001 | t0011 | g0075 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18995 | hp1 | a0004 | c0008 | t0035 | g0169 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA18998 | hp2 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19000 | hp1 | a0001 | c0001 | t0011 | g0057 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0214 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19007 | hp1 | a0001 | c0002 | t0004 | g0272 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19007 | hp2 | a0001 | c0001 | t0012 | g0303 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19010 | hp1 | a0001 | c0002 | t0016 | g0173 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19010 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0074 | AFR | LWK | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19043 | hp2 | a0001 | c0002 | t0007 | g0031 | AFR | LWK | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19054 | hp2 | a0001 | c0002 | t0007 | g0078 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19056 | hp1 | a0001 | c0001 | t0008 | g0118 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19057 | hp1 | a0001 | c0001 | t0006 | g0221 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0234 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19066 | hp1 | a0001 | c0002 | t0010 | g0198 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19066 | hp2 | a0001 | c0002 | t0010 | g0207 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0216 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19070 | hp1 | a0001 | c0007 | t0002 | g0098 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0209 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19074 | hp2 | a0001 | c0002 | t0004 | g0305 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19079 | hp1 | a0001 | c0002 | t0016 | g0229 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19081 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19082 | hp2 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0166 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0144 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19089 | hp2 | a0001 | c0002 | t0003 | g0213 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA20129 | hp1 | a0001 | c0004 | t0002 | g0045 | AFR | ASW | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0360 | AFR | ASW | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0366 | EUR | TSI | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0365 | EUR | TSI | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0162 | EUR | TSI | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | GIH | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA20905 | hp2 | a0001 | c0001 | t0024 | g0239 | SAS | GIH | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02109 | hp1 | a0001 | c0004 | t0002 | g0046 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0251 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0109 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02486 | hp2 | a0001 | c0002 | t0007 | g0052 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02559 | hp1 | a0001 | c0003 | t0014 | g0153 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0294 | AFR | ACB | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03471 | hp1 | a0001 | c0004 | t0002 | g0061 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0067 | AFR | MSL | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | USA | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | USA | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0374 | AFR | USA | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0055 | AFR | USA | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0353 | REF | REF | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0123 | REF | REF | RFLNA_chr12_124290093_124321024 | RFLNA | chr12 | 124290093 | 124321024 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:124295554 | C | G | 1 | a0004 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.125C>G | p.Ser42Cys | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/3 | 462/2487 | 125/651 | 42/216 | chr12 | 124295554 | |||
| chr12:124314265 | G | A | 1 | a0002 | 6 | HG00280.hp1 HG01099.hp1 HG02258.hp1 others(3): Show |
missense_variant | MODERATE | c.391G>A | p.Val131Ile | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 728/2487 | 391/651 | 131/216 | chr12 | 124314265 | |||
| chr12:124314317 | A | G | 1 | a0003 | 3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
missense_variant | MODERATE | c.443A>G | p.Asn148Ser | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 780/2487 | 443/651 | 148/216 | chr12 | 124314317 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:124311850 | G | A | 1 | a0001c0004 | 7 | HG02109.hp1 HG02257.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.240G>A | p.Ser80Ser | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/3 | 577/2487 | 240/651 | 80/216 | chr12 | 124311850 | |||
| chr12:124314255 | C | T | 3 | a0001c0002 a0001c0004 a0001c0007 |
150 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
synonymous_variant | LOW | c.381C>T | p.Pro127Pro | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 718/2487 | 381/651 | 127/216 | chr12 | 124314255 | |||
| chr12:124314270 | G | A | 1 | a0001c0007 | 1 | NA19070.hp1 | synonymous_variant | LOW | c.396G>A | p.Thr132Thr | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 733/2487 | 396/651 | 132/216 | chr12 | 124314270 | |||
| chr12:124314309 | G | A | 1 | a0001c0003 | 17 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(14): Show |
synonymous_variant | LOW | c.435G>A | p.Thr145Thr | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 772/2487 | 435/651 | 145/216 | chr12 | 124314309 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:124295120 | T | TCGGGGCT others(4): Show |
2 | a0001c0001t0037 a0001c0002t0016 |
5 | HG00544.hp2 NA18979.hp2 NA18993.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-306_-296dupGGCTGG others(5): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/3 | 295 | INFO_REALIGN_3_PRIME | chr12 | 124295120 | |||||
| chr12:124295169 | T | C | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(37): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
5_prime_UTR_variant | MODIFIER | c.-261T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/3 | 261 | chr12 | 124295169 | ||||||
| chr12:124295211 | G | A | 1 | a0001c0003t0036 | 1 | HG02897.hp2 | 5_prime_UTR_variant | MODIFIER | c.-219G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/3 | 219 | chr12 | 124295211 | ||||||
| chr12:124295211 | G | C | 11 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(8): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
5_prime_UTR_variant | MODIFIER | c.-219G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/3 | 219 | chr12 | 124295211 | ||||||
| chr12:124295221 | T | A | 8 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0028 others(5): Show |
85 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-209T>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/3 | 209 | chr12 | 124295221 | ||||||
| chr12:124295290 | G | A | 1 | a0001c0002t0030 | 1 | HG02451.hp1 | 5_prime_UTR_variant | MODIFIER | c.-140G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/3 | 140 | chr12 | 124295290 | ||||||
| chr12:124295384 | G | A | 1 | a0001c0002t0031 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/3 | 46 | chr12 | 124295384 | ||||||
| chr12:124314556 | GAGCCGGG others(13): Show |
G | 1 | a0001c0002t0019 | 3 | HG02451.hp2 HG03225.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*41_*60delCCCTGGGG others(12): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 41 | INFO_REALIGN_3_PRIME | chr12 | 124314556 | |||||
| chr12:124314612 | A | C | 1 | a0003c0006t0018 | 3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*87A>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 87 | chr12 | 124314612 | ||||||
| chr12:124314613 | C | A | 6 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0013 others(3): Show |
34 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*88C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 88 | chr12 | 124314613 | ||||||
| chr12:124314627 | G | A | 1 | a0001c0001t0024 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 102 | chr12 | 124314627 | ||||||
| chr12:124314642 | C | T | 1 | a0003c0006t0018 | 3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*117C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 117 | chr12 | 124314642 | ||||||
| chr12:124314677 | C | G | 1 | a0003c0006t0018 | 3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*152C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 152 | chr12 | 124314677 | ||||||
| chr12:124314778 | G | A | 1 | a0003c0006t0018 | 3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*253G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 253 | chr12 | 124314778 | ||||||
| chr12:124314841 | G | A | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(14): Show |
189 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*316G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 316 | chr12 | 124314841 | ||||||
| chr12:124314870 | G | A | 3 | a0001c0001t0011 a0001c0001t0026 a0001c0001t0029 |
9 | HG02129.hp1 HG03654.hp1 HG03704.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*345G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 345 | chr12 | 124314870 | ||||||
| chr12:124314906 | G | A | 1 | a0001c0003t0014 | 5 | HG02559.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*381G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 381 | chr12 | 124314906 | ||||||
| chr12:124314912 | G | A | 10 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(7): Show |
152 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*387G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 387 | chr12 | 124314912 | ||||||
| chr12:124314953 | C | T | 1 | a0003c0006t0018 | 3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*428C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 428 | chr12 | 124314953 | ||||||
| chr12:124314954 | T | G | 1 | a0003c0006t0018 | 3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*429T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 429 | chr12 | 124314954 | ||||||
| chr12:124315053 | G | T | 1 | a0003c0006t0018 | 3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*528G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 528 | chr12 | 124315053 | ||||||
| chr12:124315063 | A | G | 1 | a0003c0006t0018 | 3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*538A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 538 | chr12 | 124315063 | ||||||
| chr12:124315096 | C | T | 28 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(25): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*571C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 571 | chr12 | 124315096 | ||||||
| chr12:124315203 | G | A | 1 | a0001c0001t0033 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*678G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 678 | chr12 | 124315203 | ||||||
| chr12:124315229 | A | G | 1 | a0003c0006t0018 | 3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*704A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 704 | chr12 | 124315229 | ||||||
| chr12:124315252 | G | A | 1 | a0001c0002t0027 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*727G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 727 | chr12 | 124315252 | ||||||
| chr12:124315402 | C | A | 1 | a0001c0001t0028 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*877C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 877 | chr12 | 124315402 | ||||||
| chr12:124315414 | C | T | 1 | a0001c0003t0014 | 5 | HG02559.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*889C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 889 | chr12 | 124315414 | ||||||
| chr12:124315488 | C | T | 1 | a0001c0002t0020 | 2 | HG00408.hp2 NA18948.hp1 |
3_prime_UTR_variant | MODIFIER | c.*963C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 963 | chr12 | 124315488 | ||||||
| chr12:124315609 | C | T | 1 | a0001c0001t0015 | 4 | HG01257.hp2 HG01258.hp2 HG01433.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1084C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 1084 | chr12 | 124315609 | ||||||
| chr12:124315618 | G | C | 13 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0013 others(10): Show |
71 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1093G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 1093 | chr12 | 124315618 | ||||||
| chr12:124315651 | G | GAGCCCAC others(10): Show |
1 | a0001c0001t0034 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1131_*1132insACAG others(13): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 1132 | INFO_REALIGN_3_PRIME | chr12 | 124315651 | |||||
| chr12:124315694 | C | T | 1 | a0001c0001t0025 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1169C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 1169 | chr12 | 124315694 | ||||||
| chr12:124315772 | T | C | 22 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(19): Show |
200 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*1247T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 1247 | chr12 | 124315772 | ||||||
| chr12:124315866 | G | T | 2 | a0001c0002t0017 a0001c0002t0022 |
5 | HG01243.hp1 HG02647.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1341G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 1341 | chr12 | 124315866 | ||||||
| chr12:124315874 | G | A | 1 | a0001c0001t0021 | 2 | HG02055.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1349G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 3/3 | 1349 | chr12 | 124315874 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:124295655 | T | C | 28 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(25): Show |
29 | HG00280.hp1 HG00558.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.207+19T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295655 | |||||||
| chr12:124295658 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.207+22C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295658 | |||||||
| chr12:124295685 | G | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
7 | HG00673.hp2 HG02027.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+49G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295685 | |||||||
| chr12:124295729 | G | T | 6 | a0001c0002t0004g0373 a0001c0002t0004g0374 a0001c0002t0004g0375 others(3): Show |
6 | HG01255.hp1 HG01934.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+93G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295729 | |||||||
| chr12:124295732 | CCT | C | 32 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0011g0002 others(29): Show |
33 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.207+98_207+99delTC | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124295732 | ||||||
| chr12:124295748 | C | A | 1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+112C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295748 | |||||||
| chr12:124295753 | CAACCACG others(56): Show |
C | 1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+118_207+180del others(63): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295753 | |||||||
| chr12:124295757 | C | T | 27 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(24): Show |
28 | HG00280.hp1 HG00558.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.207+121C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295757 | |||||||
| chr12:124295801 | G | T | 3 | a0001c0002t0007g0083 a0001c0002t0007g0087 a0001c0002t0007g0099 |
3 | NA18939.hp1 NA18946.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.207+165G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295801 | |||||||
| chr12:124295820 | A | T | 1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+184A>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295820 | |||||||
| chr12:124295826 | G | A | 34 | a0001c0001t0005g0094 a0001c0001t0005g0102 a0001c0001t0005g0103 others(31): Show |
35 | HG01070.hp1 HG01071.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.207+190G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295826 | |||||||
| chr12:124295859 | G | T | 1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+223G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295859 | |||||||
| chr12:124295860 | T | G | 1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+224T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295860 | |||||||
| chr12:124295873 | A | G | 1 | a0001c0002t0007g0372 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.207+237A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124295873 | |||||||
| chr12:124296030 | G | A | 5 | a0001c0002t0002g0049 a0001c0004t0002g0045 a0001c0004t0002g0046 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+394G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296030 | |||||||
| chr12:124296072 | T | TTTTCTTT others(5): Show |
3 | a0001c0003t0009g0005 a0001c0003t0009g0132 a0001c0003t0036g0133 |
4 | HG02280.hp2 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+478_207+489dup others(12): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(8): Show |
5 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(2): Show |
5 | HG01358.hp2 HG01943.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+450_207+451ins others(15): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(12): Show |
1 | a0001c0001t0006g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.207+450_207+451ins others(19): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(16): Show |
1 | a0001c0001t0006g0004 | 2 | HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.207+450_207+451ins others(23): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(20): Show |
1 | a0001c0001t0008g0113 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.207+450_207+451ins others(27): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(24): Show |
7 | a0001c0001t0006g0111 a0001c0001t0006g0112 a0001c0001t0008g0114 others(4): Show |
7 | HG00735.hp1 HG01109.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.207+450_207+451ins others(31): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(9): Show |
2 | a0001c0003t0009g0006 a0001c0003t0009g0164 |
3 | HG02970.hp2 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.207+474_207+489dup others(16): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(13): Show |
3 | a0001c0002t0023g0192 a0001c0002t0023g0193 a0001c0003t0009g0194 |
3 | HG02717.hp1 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.207+470_207+489dup others(20): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(43): Show |
1 | a0001c0001t0011g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.207+469_207+470ins others(50): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(29): Show |
1 | a0001c0001t0006g0231 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.207+454_207+489dup others(36): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(51): Show |
1 | a0001c0001t0011g0051 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.207+477_207+478ins others(58): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(51): Show |
1 | a0001c0001t0011g0057 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.207+475_207+476ins others(58): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(39): Show |
1 | a0001c0002t0002g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.207+471_207+472ins others(46): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296072 | T | TTTTCTTT others(35): Show |
1 | a0001c0001t0011g0070 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.207+467_207+468ins others(42): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296072 | ||||||
| chr12:124296073 | T | TTTCTTTC others(4): Show |
3 | a0001c0001t0005g0013 a0001c0002t0007g0012 a0001c0002t0030g0011 |
3 | HG02451.hp1 HG03225.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.207+440_207+450dup others(11): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296073 | ||||||
| chr12:124296076 | C | CTTTCTTT others(38): Show |
1 | a0001c0001t0012g0294 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.207+443_207+487dup others(45): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296076 | ||||||
| chr12:124296076 | C | CTTTCTTT others(68): Show |
1 | a0001c0001t0001g0343 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.207+483_207+484ins others(75): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296076 | ||||||
| chr12:124296080 | C | CTTTCTTT others(40): Show |
1 | a0001c0001t0001g0010 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.207+475_207+476ins others(47): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296080 | ||||||
| chr12:124296081 | T | TTTC | 20 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0021 others(17): Show |
21 | HG00280.hp1 HG00558.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.207+448_207+450dup others(3): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296081 | ||||||
| chr12:124296084 | C | CTTTCTTT others(7): Show |
1 | a0001c0002t0010g0370 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.207+450_207+463dup others(14): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296084 | ||||||
| chr12:124296084 | C | CTTTCTTT others(60): Show |
1 | a0001c0001t0001g0342 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.207+483_207+484ins others(67): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296084 | ||||||
| chr12:124296084 | C | CTTTCTTT others(64): Show |
1 | a0001c0001t0015g0337 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.207+483_207+484ins others(71): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296084 | ||||||
| chr12:124296084 | C | CTTTCTTT others(52): Show |
2 | a0001c0001t0001g0367 a0001c0001t0001g0368 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.207+479_207+480ins others(59): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296084 | ||||||
| chr12:124296088 | C | CTTTCTTT others(22): Show |
1 | a0001c0002t0004g0378 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.207+455_207+483dup others(29): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296088 | ||||||
| chr12:124296088 | C | CTTTCTTT others(26): Show |
1 | a0001c0002t0004g0377 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.207+455_207+487dup others(33): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296088 | ||||||
| chr12:124296088 | C | CTTTCTTT others(52): Show |
4 | a0001c0001t0001g0348 a0001c0001t0001g0350 a0001c0001t0001g0352 others(1): Show |
4 | HG00408.hp1 HG01175.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+483_207+484ins others(59): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296088 | ||||||
| chr12:124296088 | C | CTTTCTTT others(56): Show |
1 | a0001c0001t0001g0341 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.207+483_207+484ins others(63): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296088 | ||||||
| chr12:124296088 | C | CTTTCTTT others(60): Show |
1 | a0001c0001t0001g0336 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.207+483_207+484ins others(67): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296088 | ||||||
| chr12:124296088 | C | CTTTCTTT others(48): Show |
2 | a0001c0001t0001g0365 a0001c0001t0001g0366 |
2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.207+479_207+480ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296088 | ||||||
| chr12:124296088 | C | CTTTCTTT others(56): Show |
1 | a0001c0001t0001g0354 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.207+479_207+480ins others(63): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296088 | ||||||
| chr12:124296090 | T | TTCTTTCT others(112): Show |
1 | a0001c0002t0002g0077 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.207+470_207+471ins others(119): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296090 | ||||||
| chr12:124296092 | C | CTTTCTTT others(48): Show |
2 | a0001c0001t0001g0044 a0001c0002t0004g0349 |
2 | HG02080.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.207+483_207+484ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296092 | ||||||
| chr12:124296092 | C | CTTTCTTT others(52): Show |
5 | a0001c0001t0001g0042 a0001c0001t0001g0338 a0001c0001t0001g0339 others(2): Show |
5 | HG02074.hp1 HG02080.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+483_207+484ins others(59): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296092 | ||||||
| chr12:124296092 | C | CTTTCTTT others(44): Show |
4 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0364 others(1): Show |
4 | HG01074.hp1 HG01934.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+479_207+480ins others(51): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296092 | ||||||
| chr12:124296092 | C | CTTTCTTT others(48): Show |
2 | a0001c0001t0001g0355 a0001c0001t0001g0356 |
2 | HG00438.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.207+479_207+480ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296092 | ||||||
| chr12:124296094 | T | TTCTTTTT others(108): Show |
1 | a0001c0002t0031g0371 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.207+463_207+464ins others(115): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296094 | ||||||
| chr12:124296096 | C | CTTTCTTT others(44): Show |
3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG00558.hp2 HG01074.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.207+483_207+484ins others(51): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296096 | ||||||
| chr12:124296096 | C | CTTTCTTT others(56): Show |
1 | a0001c0001t0001g0332 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.207+483_207+484ins others(63): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296096 | ||||||
| chr12:124296096 | C | CTTTCTTT others(40): Show |
3 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0004g0360 |
3 | HG01433.hp1 HG01952.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.207+479_207+480ins others(47): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296096 | ||||||
| chr12:124296096 | C | CTTTCTTT others(32): Show |
1 | a0001c0001t0001g0369 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.207+471_207+472ins others(39): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296096 | ||||||
| chr12:124296100 | C | CTT | 6 | a0001c0002t0002g0068 a0001c0002t0002g0073 a0001c0002t0002g0074 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+466_207+467dup others(2): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(40): Show |
1 | a0001c0001t0026g0344 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.207+483_207+484ins others(47): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(36): Show |
1 | a0001c0001t0012g0357 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.207+479_207+480ins others(43): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(48): Show |
3 | a0001c0001t0005g0058 a0001c0001t0021g0059 a0001c0001t0021g0060 |
3 | HG02055.hp2 HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.207+475_207+476ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(52): Show |
1 | a0001c0002t0002g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+475_207+476ins others(59): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(56): Show |
3 | a0001c0004t0002g0046 a0001c0004t0002g0047 a0001c0004t0002g0048 |
3 | HG02109.hp1 HG02257.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.207+475_207+476ins others(63): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(60): Show |
1 | a0001c0004t0002g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.207+475_207+476ins others(67): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(40): Show |
1 | a0001c0004t0002g0067 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.207+471_207+472ins others(47): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(48): Show |
2 | a0002c0005t0005g0065 a0002c0005t0005g0066 |
2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.207+471_207+472ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(52): Show |
1 | a0002c0005t0005g0064 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.207+471_207+472ins others(59): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(60): Show |
1 | a0002c0005t0005g0062 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.207+471_207+472ins others(67): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296100 | C | CTTTCTTT others(64): Show |
1 | a0001c0004t0002g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.207+471_207+472ins others(71): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296100 | ||||||
| chr12:124296104 | C | T | 2 | a0001c0001t0011g0002 a0001c0001t0011g0075 |
3 | NA18951.hp2 NA18994.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.207+468C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296104 | |||||||
| chr12:124296118 | T | TTCTTTTC others(54): Show |
1 | a0001c0002t0004g0293 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.207+487_207+488ins others(61): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296118 | ||||||
| chr12:124296118 | T | TTTTCTTT others(80): Show |
1 | a0001c0001t0005g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.207+483_207+484ins others(87): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296118 | ||||||
| chr12:124296118 | T | TTTTCTTT others(72): Show |
1 | a0001c0001t0001g0333 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.207+483_207+484ins others(79): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296118 | ||||||
| chr12:124296118 | T | TTTTCTTT others(76): Show |
1 | a0001c0001t0001g0334 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.207+483_207+484ins others(83): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296118 | ||||||
| chr12:124296118 | T | TTTTCTTT others(80): Show |
1 | a0001c0001t0001g0335 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.207+483_207+484ins others(87): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296118 | ||||||
| chr12:124296122 | T | TTCTTTCT others(13): Show |
1 | a0001c0003t0014g0168 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(20): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296122 | ||||||
| chr12:124296122 | T | TTTTCTTT others(78): Show |
1 | a0001c0001t0001g0331 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.207+487_207+488ins others(85): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296122 | ||||||
| chr12:124296124 | C | CTTTCCTT others(48): Show |
1 | a0001c0002t0004g0127 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(7): Show |
1 | a0001c0001t0006g0165 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(14): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(19): Show |
1 | a0004c0008t0035g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(26): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(103): Show |
2 | a0001c0002t0002g0107 a0001c0002t0002g0108 |
2 | NA18995.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.207+489_207+490ins others(110): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(27): Show |
1 | a0001c0002t0003g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(34): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(25): Show |
4 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0002t0002g0020 others(1): Show |
4 | HG02280.hp1 HG03239.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+489_207+490ins others(32): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(31): Show |
8 | a0001c0001t0006g0205 a0001c0001t0006g0206 a0001c0001t0006g0211 others(5): Show |
8 | HG02300.hp2 NA18961.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+489_207+490ins others(38): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(29): Show |
5 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0036 others(2): Show |
6 | HG00280.hp1 HG01106.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+489_207+490ins others(36): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(35): Show |
7 | a0001c0001t0006g0218 a0001c0001t0008g0217 a0001c0002t0003g0213 others(4): Show |
7 | HG00323.hp2 HG00673.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+489_207+490ins others(42): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(33): Show |
3 | a0001c0002t0002g0027 a0001c0002t0007g0025 a0003c0006t0018g0026 |
3 | HG00558.hp1 HG01891.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.207+489_207+490ins others(40): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(39): Show |
12 | a0001c0001t0006g0221 a0001c0001t0006g0222 a0001c0001t0006g0226 others(9): Show |
13 | HG01496.hp2 HG02056.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.207+489_207+490ins others(46): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(37): Show |
3 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0005g0028 |
3 | HG01943.hp1 HG03710.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.207+489_207+490ins others(44): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(42): Show |
1 | a0001c0001t0033g0032 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(49): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(43): Show |
4 | a0001c0001t0006g0232 a0001c0002t0003g0233 a0001c0002t0003g0234 others(1): Show |
4 | HG02083.hp2 HG03669.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+489_207+490ins others(50): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(41): Show |
2 | a0001c0001t0002g0037 a0003c0006t0018g0033 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.207+489_207+490ins others(48): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(47): Show |
1 | a0001c0002t0003g0236 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(54): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(45): Show |
1 | a0001c0001t0002g0034 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(52): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(49): Show |
1 | a0003c0006t0018g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(56): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(43): Show |
3 | a0001c0001t0001g0240 a0001c0001t0024g0239 a0001c0002t0020g0238 |
3 | HG02818.hp2 NA18948.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.207+489_207+490ins others(50): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(47): Show |
1 | a0001c0002t0004g0237 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(54): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(67): Show |
1 | a0001c0001t0001g0243 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(74): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(71): Show |
1 | a0001c0001t0001g0242 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(78): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(67): Show |
1 | a0001c0002t0007g0052 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(74): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(63): Show |
2 | a0001c0001t0011g0075 a0001c0002t0022g0053 |
2 | HG01243.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.207+489_207+490ins others(70): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(59): Show |
2 | a0001c0001t0011g0002 a0001c0002t0002g0068 |
3 | HG02258.hp2 NA18951.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.207+489_207+490ins others(66): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(64): Show |
1 | a0001c0001t0001g0244 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(71): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(68): Show |
1 | a0001c0001t0001g0245 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(75): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(55): Show |
1 | a0001c0003t0014g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(62): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(72): Show |
1 | a0002c0005t0005g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(79): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(47): Show |
1 | a0001c0002t0022g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(54): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(43): Show |
3 | a0001c0002t0002g0073 a0001c0002t0002g0074 a0001c0003t0014g0072 |
3 | HG02818.hp1 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.207+489_207+490ins others(50): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(39): Show |
1 | a0001c0002t0002g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(46): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(31): Show |
1 | a0001c0001t0005g0246 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(38): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(70): Show |
1 | a0001c0001t0001g0247 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(77): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(32): Show |
1 | a0001c0002t0004g0252 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(39): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(36): Show |
2 | a0001c0002t0004g0253 a0001c0002t0004g0373 |
2 | HG01934.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.207+489_207+490ins others(43): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(40): Show |
1 | a0001c0002t0020g0255 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(47): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(100): Show |
1 | a0001c0001t0001g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(107): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(60): Show |
1 | a0001c0002t0004g0374 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(67): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(114): Show |
1 | a0001c0001t0001g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(121): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(36): Show |
3 | a0001c0001t0005g0258 a0001c0002t0004g0259 a0001c0002t0004g0375 |
3 | HG01169.hp2 HG02273.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.207+489_207+490ins others(43): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(48): Show |
1 | a0001c0002t0017g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(40): Show |
2 | a0001c0002t0017g0260 a0001c0002t0017g0261 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.207+489_207+490ins others(47): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(44): Show |
1 | a0001c0002t0004g0263 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(51): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(90): Show |
1 | a0001c0002t0004g0262 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(97): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(48): Show |
1 | a0001c0002t0004g0264 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(53): Show |
1 | a0001c0002t0004g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(60): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(58): Show |
1 | a0001c0001t0001g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(65): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTCTTT others(62): Show |
2 | a0001c0001t0001g0271 a0001c0002t0004g0272 |
2 | NA18945.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.207+489_207+490ins others(69): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTTCTT others(28): Show |
1 | a0001c0002t0004g0376 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(35): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTTCTT others(32): Show |
1 | a0001c0002t0027g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(39): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTTCTT others(44): Show |
1 | a0001c0002t0004g0274 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(51): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTTCTT others(102): Show |
1 | a0001c0001t0012g0275 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(109): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTTCTT others(56): Show |
1 | a0001c0001t0001g0276 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.207+489_207+490ins others(63): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTTCTT others(69): Show |
1 | a0001c0001t0001g0277 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(76): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTTTCT others(66): Show |
1 | a0001c0001t0001g0290 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(73): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTTTCT others(70): Show |
1 | a0001c0001t0001g0291 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(77): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | CTTTTTCT others(74): Show |
1 | a0001c0001t0001g0292 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.207+489_207+490ins others(81): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296124 | ||||||
| chr12:124296124 | C | T | 57 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(54): Show |
58 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.207+488C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296124 | |||||||
| chr12:124296126 | C | T | 181 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0042 others(178): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.207+490C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296126 | |||||||
| chr12:124296128 | C | T | 108 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(105): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.207+492C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296128 | |||||||
| chr12:124296130 | C | T | 148 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0042 others(145): Show |
151 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.207+494C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296130 | |||||||
| chr12:124296132 | C | CTTCTTTC others(36): Show |
1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+497_207+498ins others(43): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296132 | ||||||
| chr12:124296132 | C | T | 70 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(67): Show |
71 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.207+496C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296132 | |||||||
| chr12:124296134 | C | T | 96 | a0001c0001t0001g0038 a0001c0001t0001g0151 a0001c0001t0001g0156 others(93): Show |
97 | HG00438.hp2 HG00544.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.207+498C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296134 | |||||||
| chr12:124296136 | C | T | 78 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0041 others(75): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.207+500C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296136 | |||||||
| chr12:124296137 | TC | T | 42 | a0001c0001t0001g0038 a0001c0001t0001g0181 a0001c0001t0001g0199 others(39): Show |
43 | HG00544.hp2 HG00642.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.207+502delC | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296137 | |||||||
| chr12:124296138 | C | T | 42 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0157 others(39): Show |
42 | HG00438.hp2 HG01192.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.207+502C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296138 | |||||||
| chr12:124296139 | T | TC | 4 | a0001c0001t0001g0331 a0001c0001t0008g0118 a0001c0001t0008g0134 others(1): Show |
4 | HG02698.hp1 NA18967.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+503_207+504ins others(1): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296139 | |||||||
| chr12:124296139 | T | TCTCTTTC others(117): Show |
1 | a0001c0002t0002g0086 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.207+503_207+504ins others(124): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296139 | |||||||
| chr12:124296139 | T | TCTCTTTC others(139): Show |
1 | a0001c0002t0007g0087 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.207+503_207+504ins others(146): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296139 | |||||||
| chr12:124296139 | T | TCTCTTTC others(130): Show |
1 | a0001c0002t0007g0088 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.207+503_207+504ins others(137): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296139 | |||||||
| chr12:124296139 | T | TCTTTCTC others(112): Show |
1 | a0001c0002t0002g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.207+503_207+504ins others(119): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296139 | |||||||
| chr12:124296139 | T | TCTTTCTT others(122): Show |
1 | a0001c0001t0013g0090 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.207+503_207+504ins others(129): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296139 | |||||||
| chr12:124296139 | T | TCTTTCTT others(146): Show |
1 | a0001c0002t0002g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.207+503_207+504ins others(153): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296139 | |||||||
| chr12:124296139 | T | TCTTTCTT others(151): Show |
1 | a0001c0002t0002g0092 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.207+503_207+504ins others(158): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296139 | |||||||
| chr12:124296139 | T | TCTTTCTT others(171): Show |
1 | a0001c0002t0002g0093 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.207+503_207+504ins others(178): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296139 | |||||||
| chr12:124296139 | T | TCTTTCTT others(134): Show |
1 | a0001c0001t0005g0094 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.207+503_207+504ins others(141): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296139 | |||||||
| chr12:124296139 | T | TTCTTC | 2 | a0001c0003t0009g0005 a0001c0003t0009g0120 |
3 | HG02145.hp2 HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.207+545_207+549dup others(5): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTCTTCTC others(3): Show |
1 | a0001c0003t0009g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.207+540_207+549dup others(10): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTCTTCTC others(8): Show |
1 | a0001c0002t0023g0193 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.207+535_207+549dup others(15): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTCTTCTC others(13): Show |
1 | a0001c0002t0023g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.207+530_207+549dup others(20): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(233): Show |
1 | a0001c0001t0002g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.207+504_207+505ins others(240): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(112): Show |
1 | a0001c0001t0002g0131 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.207+504_207+505ins others(119): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(117): Show |
1 | a0001c0002t0002g0081 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.207+504_207+505ins others(124): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(122): Show |
1 | a0001c0002t0002g0079 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.207+504_207+505ins others(129): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(196): Show |
1 | a0001c0002t0002g0082 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.207+504_207+505ins others(203): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(135): Show |
1 | a0001c0002t0002g0095 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.207+504_207+505ins others(142): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(102): Show |
1 | a0001c0004t0002g0270 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.207+504_207+505ins others(109): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(121): Show |
1 | a0001c0002t0007g0003 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.207+504_207+505ins others(128): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(125): Show |
1 | a0001c0002t0002g0097 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.207+504_207+505ins others(132): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(140): Show |
2 | a0001c0002t0002g0096 a0001c0002t0007g0083 |
2 | HG01928.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.207+504_207+505ins others(147): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(113): Show |
1 | a0001c0007t0002g0098 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.207+504_207+505ins others(120): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(123): Show |
1 | a0001c0002t0007g0078 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.207+504_207+505ins others(130): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(122): Show |
1 | a0001c0002t0002g0084 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.207+504_207+505ins others(129): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(144): Show |
1 | a0001c0002t0007g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.207+504_207+505ins others(151): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(123): Show |
1 | a0001c0002t0002g0100 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.207+504_207+505ins others(130): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(122): Show |
1 | a0001c0002t0007g0080 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.207+504_207+505ins others(129): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(123): Show |
1 | a0001c0002t0002g0101 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.207+504_207+505ins others(130): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(121): Show |
1 | a0001c0001t0005g0102 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.207+504_207+505ins others(128): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(121): Show |
1 | a0001c0001t0005g0103 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.207+504_207+505ins others(128): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(125): Show |
1 | a0001c0001t0005g0104 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.207+504_207+505ins others(132): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(145): Show |
2 | a0001c0002t0007g0105 a0001c0002t0007g0106 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.207+504_207+505ins others(152): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | T | TTTCTTTC others(153): Show |
1 | a0001c0002t0007g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.207+504_207+505ins others(160): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296139 | TTC | T | 4 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(1): Show |
4 | HG02735.hp2 NA18993.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+505_207+506del others(2): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296139 | ||||||
| chr12:124296140 | T | C | 133 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0044 others(130): Show |
136 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.207+504T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296140 | |||||||
| chr12:124296141 | C | T | 303 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0039 others(300): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.207+505C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296141 | |||||||
| chr12:124296142 | T | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(129): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.207+506T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296142 | |||||||
| chr12:124296142 | T | TC | 7 | a0001c0001t0001g0331 a0001c0001t0008g0118 a0001c0001t0008g0134 others(4): Show |
7 | HG02698.hp1 NA18966.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+506_207+507ins others(1): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296142 | |||||||
| chr12:124296142 | T | TTTCTTTC others(50): Show |
1 | a0001c0002t0004g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.207+507_207+508ins others(57): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296142 | ||||||
| chr12:124296143 | T | TTCTTTCT others(59): Show |
1 | a0001c0002t0003g0212 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.207+507_207+508ins others(66): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296143 | |||||||
| chr12:124296143 | TC | T | 20 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0199 others(17): Show |
20 | HG01167.hp1 HG01167.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.207+508delC | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296143 | |||||||
| chr12:124296144 | C | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0040 others(87): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.207+508C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296144 | |||||||
| chr12:124296145 | T | C | 20 | a0001c0001t0001g0038 a0001c0001t0001g0181 a0001c0001t0006g0170 others(17): Show |
21 | HG00544.hp2 HG00642.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.207+509T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296145 | |||||||
| chr12:124296145 | TC | T | 4 | a0001c0001t0005g0249 a0001c0001t0013g0250 a0001c0002t0002g0248 others(1): Show |
4 | HG00735.hp2 HG02109.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+510delC | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296145 | |||||||
| chr12:124296146 | C | CTCTCTCT others(38): Show |
1 | a0001c0001t0008g0114 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.207+511_207+512ins others(45): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296146 | ||||||
| chr12:124296146 | C | CTTTCTTT others(2): Show |
3 | a0001c0002t0003g0228 a0001c0002t0016g0229 a0001c0002t0016g0230 |
3 | NA18993.hp2 NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.207+512_207+513ins others(9): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296146 | ||||||
| chr12:124296146 | C | CTTTCTTT others(10): Show |
1 | a0001c0001t0008g0227 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.207+512_207+513ins others(17): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296146 | ||||||
| chr12:124296146 | C | T | 82 | a0001c0001t0001g0038 a0001c0001t0001g0151 a0001c0001t0001g0181 others(79): Show |
85 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.207+510C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296146 | |||||||
| chr12:124296147 | T | TC | 121 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0042 others(118): Show |
122 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.207+511_207+512ins others(1): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296147 | |||||||
| chr12:124296147 | T | TCTC | 8 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(5): Show |
8 | HG01358.hp2 HG01943.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+511_207+512ins others(3): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296147 | |||||||
| chr12:124296147 | T | TCTCTC | 4 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(1): Show |
5 | HG01109.hp2 HG01891.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+511_207+512ins others(5): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296147 | |||||||
| chr12:124296147 | T | TCTTTCTT others(6): Show |
1 | a0001c0001t0005g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.207+511_207+512ins others(13): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296147 | |||||||
| chr12:124296147 | T | TCTTTCTT others(102): Show |
1 | a0001c0001t0001g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.207+511_207+512ins others(109): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296147 | |||||||
| chr12:124296147 | T | TTTC | 4 | a0001c0001t0001g0269 a0001c0001t0006g0205 a0001c0001t0006g0221 others(1): Show |
4 | HG02148.hp1 NA18961.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+512_207+513ins others(3): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296147 | ||||||
| chr12:124296147 | T | TTTCTTTC | 24 | a0001c0001t0006g0206 a0001c0001t0006g0211 a0001c0001t0006g0218 others(21): Show |
25 | HG00323.hp2 HG00673.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.207+512_207+513ins others(7): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296147 | ||||||
| chr12:124296147 | T | TTTCTTTC others(4): Show |
2 | a0001c0002t0002g0055 a0002c0005t0005g0054 |
2 | HG02258.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.207+512_207+513ins others(11): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296147 | ||||||
| chr12:124296147 | T | TTTCTTTC others(8): Show |
1 | a0001c0002t0017g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.207+512_207+513ins others(15): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296147 | ||||||
| chr12:124296147 | T | TTTCTTTC others(100): Show |
1 | a0001c0001t0013g0126 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.207+512_207+513ins others(107): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296147 | ||||||
| chr12:124296148 | TC | T | 45 | a0001c0001t0001g0041 a0001c0001t0001g0156 a0001c0001t0001g0157 others(42): Show |
45 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.207+513delC | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296148 | |||||||
| chr12:124296149 | C | T | 95 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0151 others(92): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.207+513C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296149 | |||||||
| chr12:124296150 | T | C | 55 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0199 others(52): Show |
57 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.207+514T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296150 | |||||||
| chr12:124296150 | T | TTTC | 3 | a0001c0002t0003g0228 a0001c0002t0016g0229 a0001c0002t0016g0230 |
3 | NA18993.hp2 NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.207+514_207+515ins others(3): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296150 | |||||||
| chr12:124296151 | C | CT | 7 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(4): Show |
8 | HG01109.hp2 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+517dupT | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296151 | ||||||
| chr12:124296151 | C | CTCTCTCT others(28): Show |
1 | a0001c0001t0008g0113 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.207+516_207+517ins others(35): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296151 | ||||||
| chr12:124296151 | C | CTCTCTCT others(32): Show |
3 | a0001c0001t0008g0115 a0001c0001t0008g0116 a0001c0001t0008g0117 |
3 | HG01361.hp2 HG01928.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.207+516_207+517ins others(39): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296151 | ||||||
| chr12:124296151 | C | CTCTCTTT others(30): Show |
1 | a0001c0001t0006g0231 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.207+516_207+517ins others(37): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296151 | ||||||
| chr12:124296151 | C | T | 128 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0040 others(125): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.207+515C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296151 | |||||||
| chr12:124296152 | T | TC | 122 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0042 others(119): Show |
124 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.207+516_207+517ins others(1): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296152 | |||||||
| chr12:124296152 | T | TCTTTCTT others(100): Show |
1 | a0001c0001t0013g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.207+516_207+517ins others(107): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296152 | |||||||
| chr12:124296152 | T | TCTTTCTT others(104): Show |
1 | a0001c0002t0002g0251 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.207+516_207+517ins others(111): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296152 | |||||||
| chr12:124296152 | T | TCTTTCTT others(115): Show |
1 | a0001c0002t0019g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.207+516_207+517ins others(122): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296152 | |||||||
| chr12:124296152 | T | TTTC | 7 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(4): Show |
7 | HG01358.hp2 HG01943.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+517_207+518ins others(3): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296152 | ||||||
| chr12:124296152 | T | TTTTCTTT others(103): Show |
1 | a0001c0003t0014g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.207+517_207+518ins others(110): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296152 | ||||||
| chr12:124296152 | T | TTTTCTTT others(103): Show |
1 | a0001c0002t0019g0186 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.207+517_207+518ins others(110): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296152 | ||||||
| chr12:124296153 | T | C | 1 | a0001c0001t0008g0227 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.207+517T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296153 | |||||||
| chr12:124296153 | TC | T | 14 | a0001c0001t0005g0129 a0001c0001t0005g0158 a0001c0001t0005g0159 others(11): Show |
14 | HG01099.hp2 HG02040.hp1 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.207+518delC | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296153 | |||||||
| chr12:124296154 | C | CTT | 23 | a0001c0001t0001g0040 a0001c0001t0001g0266 a0001c0001t0001g0296 others(20): Show |
23 | HG00673.hp2 HG01243.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.207+519_207+520ins others(2): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296154 | ||||||
| chr12:124296154 | C | CTTTCTTT others(7): Show |
2 | a0001c0001t0011g0002 a0001c0001t0011g0075 |
3 | NA18951.hp2 NA18994.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.207+519_207+520ins others(14): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296154 | ||||||
| chr12:124296154 | C | T | 72 | a0001c0001t0001g0041 a0001c0001t0001g0156 a0001c0001t0001g0157 others(69): Show |
73 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.207+518C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296154 | |||||||
| chr12:124296155 | T | C | 52 | a0001c0001t0001g0041 a0001c0001t0001g0156 a0001c0001t0001g0157 others(49): Show |
53 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.207+519T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296155 | |||||||
| chr12:124296155 | TC | T | 49 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0240 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.207+520delC | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296155 | |||||||
| chr12:124296156 | C | CT | 58 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0044 others(55): Show |
59 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.207+522dupT | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296156 | ||||||
| chr12:124296156 | C | CTCTCTCT others(54): Show |
1 | a0001c0002t0003g0150 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.207+521_207+522ins others(61): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296156 | ||||||
| chr12:124296156 | C | CTCTCTCT others(50): Show |
1 | a0001c0001t0006g0170 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.207+521_207+522ins others(57): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296156 | ||||||
| chr12:124296156 | C | CTCTCTTT others(48): Show |
1 | a0001c0002t0003g0171 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.207+521_207+522ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296156 | ||||||
| chr12:124296156 | C | CTTTCTCT others(44): Show |
1 | a0001c0001t0006g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.207+522_207+523ins others(51): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296156 | ||||||
| chr12:124296156 | C | CTTTCTCT others(26): Show |
2 | a0001c0001t0006g0165 a0001c0001t0008g0110 |
2 | NA18906.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.207+522_207+523ins others(33): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296156 | ||||||
| chr12:124296156 | C | CTTTCTTT others(10): Show |
1 | a0001c0001t0008g0118 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.207+522_207+523ins others(17): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296156 | ||||||
| chr12:124296156 | C | CTTTCTTT others(102): Show |
1 | a0001c0001t0001g0285 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.207+522_207+523ins others(109): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296156 | ||||||
| chr12:124296156 | C | T | 160 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0156 others(157): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.207+520C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296156 | |||||||
| chr12:124296156 | CT | C | 10 | a0001c0001t0006g0172 a0001c0001t0006g0178 a0001c0001t0037g0174 others(7): Show |
11 | HG00544.hp2 HG00642.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+522delT | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296156 | ||||||
| chr12:124296157 | T | TC | 8 | a0001c0001t0008g0134 a0001c0001t0008g0167 a0001c0001t0008g0197 others(5): Show |
8 | HG02886.hp1 HG03195.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+521_207+522ins others(1): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TCTTTCTT others(104): Show |
1 | a0001c0002t0004g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.207+521_207+522ins others(111): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TCTTTCTT others(118): Show |
1 | a0001c0002t0004g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.207+521_207+522ins others(125): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TCTTTCTT others(30): Show |
1 | a0001c0001t0001g0333 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.207+521_207+522ins others(37): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TCTTTCTT others(104): Show |
1 | a0001c0001t0005g0249 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.207+521_207+522ins others(111): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TCTTTCTT others(34): Show |
3 | a0001c0002t0002g0128 a0001c0002t0004g0265 a0001c0002t0004g0374 |
3 | HG02698.hp1 HG03834.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.207+521_207+522ins others(41): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TCTTTCTT others(42): Show |
1 | a0001c0002t0004g0293 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.207+521_207+522ins others(49): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TCTTTCTT others(50): Show |
2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.207+521_207+522ins others(57): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TCTTTCTT others(117): Show |
1 | a0001c0002t0007g0372 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.207+521_207+522ins others(124): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TCTTTCTT others(115): Show |
1 | a0001c0001t0005g0200 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.207+521_207+522ins others(122): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TCTTTTTT others(103): Show |
1 | a0001c0002t0007g0201 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.207+521_207+522ins others(110): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296157 | |||||||
| chr12:124296157 | T | TTTCTTTC | 4 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(1): Show |
5 | HG01109.hp2 HG01891.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+522_207+523ins others(7): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296157 | ||||||
| chr12:124296157 | T | TTTCTTTC others(112): Show |
2 | a0001c0001t0001g0286 a0001c0001t0001g0322 |
2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.207+522_207+523ins others(119): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296157 | ||||||
| chr12:124296157 | T | TTTCTTTC others(112): Show |
1 | a0001c0001t0001g0269 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.207+522_207+523ins others(119): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296157 | ||||||
| chr12:124296157 | T | TTTCTTTC others(114): Show |
1 | a0001c0002t0004g0329 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.207+522_207+523ins others(121): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296157 | ||||||
| chr12:124296157 | T | TTTCTTTC others(104): Show |
1 | a0001c0003t0014g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.207+522_207+523ins others(111): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296157 | ||||||
| chr12:124296158 | T | C | 3 | a0001c0002t0003g0228 a0001c0002t0016g0229 a0001c0002t0016g0230 |
3 | NA18993.hp2 NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.207+522T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296158 | |||||||
| chr12:124296158 | TC | T | 18 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(15): Show |
18 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(15): Show |
intron_variant | MODIFIER | c.207+523delC | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296158 | |||||||
| chr12:124296159 | C | CTTTCTTT others(107): Show |
1 | a0001c0001t0001g0202 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.207+524_207+525ins others(114): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296159 | ||||||
| chr12:124296159 | C | T | 46 | a0001c0001t0001g0040 a0001c0001t0001g0181 a0001c0001t0001g0199 others(43): Show |
48 | HG00673.hp2 HG01099.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.207+523C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296159 | |||||||
| chr12:124296160 | T | C | 20 | a0001c0001t0005g0129 a0001c0001t0005g0158 a0001c0001t0005g0159 others(17): Show |
21 | HG01099.hp2 HG01243.hp1 HG02129.hp2 others(18): Show |
intron_variant | MODIFIER | c.207+524T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296160 | |||||||
| chr12:124296161 | C | CTCTCTCT others(38): Show |
7 | a0001c0001t0006g0139 a0001c0001t0006g0141 a0001c0002t0003g0137 others(4): Show |
7 | HG01256.hp2 HG01258.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+526_207+527ins others(45): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296161 | ||||||
| chr12:124296161 | C | CTCTCTCT others(36): Show |
1 | a0001c0002t0016g0135 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.207+526_207+527ins others(43): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296161 | ||||||
| chr12:124296161 | C | CTCTCTCT others(32): Show |
1 | a0001c0002t0003g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.207+526_207+527ins others(39): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296161 | ||||||
| chr12:124296161 | C | CTCTCTTT others(48): Show |
3 | a0001c0001t0008g0197 a0001c0002t0003g0196 a0001c0002t0010g0198 |
3 | HG02886.hp1 NA19066.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.207+526_207+527ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296161 | ||||||
| chr12:124296161 | C | CTTTCTCT others(44): Show |
10 | a0001c0001t0006g0172 a0001c0001t0006g0178 a0001c0001t0037g0174 others(7): Show |
11 | HG00544.hp2 HG00642.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+527_207+528ins others(51): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296161 | ||||||
| chr12:124296161 | C | CTTTCTTT others(54): Show |
1 | a0001c0001t0001g0348 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(61): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296161 | ||||||
| chr12:124296161 | C | T | 193 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0041 others(190): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.207+525C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296161 | |||||||
| chr12:124296162 | T | TC | 16 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0005g0056 others(13): Show |
16 | HG00438.hp2 HG02132.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.207+526_207+527ins others(1): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(96): Show |
1 | a0001c0002t0004g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.207+526_207+527ins others(103): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(102): Show |
1 | a0001c0001t0001g0156 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.207+526_207+527ins others(109): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(106): Show |
1 | a0001c0001t0001g0157 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.207+526_207+527ins others(113): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(100): Show |
1 | a0001c0002t0004g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.207+526_207+527ins others(107): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(98): Show |
4 | a0001c0001t0001g0268 a0001c0001t0001g0311 a0001c0001t0001g0312 others(1): Show |
4 | HG01169.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+526_207+527ins others(105): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(106): Show |
1 | a0001c0001t0001g0314 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.207+526_207+527ins others(113): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(118): Show |
1 | a0001c0001t0001g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.207+526_207+527ins others(125): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(122): Show |
1 | a0001c0002t0004g0305 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.207+526_207+527ins others(129): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(114): Show |
3 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0004g0306 |
3 | HG02015.hp2 NA19070.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.207+526_207+527ins others(121): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(118): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0282 a0001c0001t0004g0281 |
4 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+526_207+527ins others(125): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(126): Show |
1 | a0001c0001t0001g0283 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.207+526_207+527ins others(133): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(112): Show |
1 | a0001c0002t0004g0203 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.207+526_207+527ins others(119): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(114): Show |
1 | a0001c0001t0001g0309 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.207+526_207+527ins others(121): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(118): Show |
2 | a0001c0001t0001g0315 a0001c0002t0004g0183 |
2 | HG01243.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.207+526_207+527ins others(125): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(122): Show |
1 | a0001c0001t0001g0284 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.207+526_207+527ins others(129): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(110): Show |
1 | a0001c0001t0015g0184 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.207+526_207+527ins others(117): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(106): Show |
2 | a0001c0001t0001g0267 a0001c0001t0001g0310 |
2 | HG01175.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.207+526_207+527ins others(113): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(126): Show |
1 | a0001c0001t0001g0041 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.207+526_207+527ins others(133): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(46): Show |
1 | a0001c0001t0001g0242 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.207+526_207+527ins others(53): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(58): Show |
2 | a0001c0001t0001g0331 a0001c0002t0004g0163 |
2 | HG02145.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.207+526_207+527ins others(65): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(159): Show |
1 | a0001c0001t0001g0316 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.207+526_207+527ins others(166): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(147): Show |
1 | a0001c0001t0001g0317 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.207+526_207+527ins others(154): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTCTT others(127): Show |
1 | a0001c0001t0001g0318 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.207+526_207+527ins others(134): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TCTTTTCT others(143): Show |
1 | a0001c0002t0004g0319 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.207+526_207+527ins others(150): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296162 | |||||||
| chr12:124296162 | T | TTTCTTTC others(24): Show |
8 | a0001c0001t0005g0058 a0001c0001t0011g0070 a0001c0001t0021g0059 others(5): Show |
8 | HG01099.hp1 HG02055.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+527_207+528ins others(31): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(117): Show |
1 | a0001c0001t0001g0320 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(124): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(100): Show |
1 | a0001c0001t0001g0321 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.207+527_207+528ins others(107): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(112): Show |
2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | HG01256.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.207+527_207+528ins others(119): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(116): Show |
1 | a0001c0001t0001g0325 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.207+527_207+528ins others(123): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(124): Show |
1 | a0001c0001t0001g0326 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(131): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(128): Show |
1 | a0001c0002t0004g0295 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.207+527_207+528ins others(135): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(28): Show |
3 | a0001c0002t0017g0260 a0001c0002t0017g0261 a0002c0005t0005g0066 |
3 | HG02647.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.207+527_207+528ins others(35): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(108): Show |
1 | a0001c0001t0001g0287 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.207+527_207+528ins others(115): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(120): Show |
1 | a0001c0001t0001g0327 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(127): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(132): Show |
1 | a0001c0001t0001g0296 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(139): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(144): Show |
1 | a0001c0001t0001g0297 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(151): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(110): Show |
3 | a0001c0001t0001g0266 a0001c0001t0015g0278 a0001c0001t0015g0279 |
3 | HG01257.hp2 HG01258.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.207+527_207+528ins others(117): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(114): Show |
1 | a0001c0001t0025g0280 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.207+527_207+528ins others(121): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(111): Show |
1 | a0001c0001t0001g0199 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.207+527_207+528ins others(118): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(117): Show |
1 | a0001c0001t0001g0328 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(124): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(108): Show |
1 | a0001c0001t0001g0288 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(115): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(116): Show |
1 | a0001c0001t0001g0298 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.207+527_207+528ins others(123): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(128): Show |
5 | a0001c0001t0001g0040 a0001c0001t0001g0299 a0001c0001t0001g0300 others(2): Show |
5 | HG00673.hp2 NA18947.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+527_207+528ins others(135): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(136): Show |
1 | a0001c0001t0012g0303 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(143): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(140): Show |
1 | a0001c0001t0001g0304 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(147): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(36): Show |
2 | a0001c0001t0001g0345 a0001c0001t0001g0350 |
2 | HG00558.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.207+527_207+528ins others(43): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(116): Show |
1 | a0001c0001t0001g0289 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.207+527_207+528ins others(123): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(126): Show |
1 | a0001c0001t0001g0181 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(133): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(40): Show |
5 | a0001c0001t0001g0247 a0001c0001t0001g0338 a0001c0001t0024g0239 others(2): Show |
5 | HG00639.hp2 HG02135.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+527_207+528ins others(47): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(120): Show |
1 | a0001c0001t0001g0330 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.207+527_207+528ins others(127): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(44): Show |
12 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0346 others(9): Show |
12 | HG00408.hp2 HG01074.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+527_207+528ins others(51): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(48): Show |
17 | a0001c0001t0001g0010 a0001c0001t0001g0243 a0001c0001t0001g0244 others(14): Show |
18 | HG00408.hp1 HG00621.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.207+527_207+528ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(52): Show |
8 | a0001c0001t0001g0290 a0001c0001t0001g0347 a0001c0001t0001g0364 others(5): Show |
8 | HG01515.hp2 HG01934.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+527_207+528ins others(59): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(56): Show |
10 | a0001c0001t0001g0291 a0001c0001t0001g0341 a0001c0001t0001g0343 others(7): Show |
10 | HG00544.hp1 HG01975.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+527_207+528ins others(63): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(60): Show |
9 | a0001c0001t0001g0044 a0001c0001t0001g0292 a0001c0001t0001g0336 others(6): Show |
9 | HG01106.hp2 HG01109.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+527_207+528ins others(67): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(68): Show |
2 | a0001c0001t0001g0245 a0001c0001t0001g0340 |
2 | NA19084.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.207+527_207+528ins others(75): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296162 | T | TTTCTTTC others(72): Show |
1 | a0001c0001t0001g0332 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.207+527_207+528ins others(79): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296162 | ||||||
| chr12:124296163 | T | C | 28 | a0001c0001t0006g0205 a0001c0001t0006g0206 a0001c0001t0006g0211 others(25): Show |
29 | HG00323.hp2 HG00673.hp1 HG02056.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+527T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296163 | |||||||
| chr12:124296163 | T | TTCTTTCT others(15): Show |
1 | a0001c0002t0010g0370 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.207+527_207+528ins others(22): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296163 | |||||||
| chr12:124296163 | TC | T | 12 | a0001c0001t0001g0240 a0001c0001t0001g0356 a0001c0001t0005g0258 others(9): Show |
12 | HG00438.hp1 HG01169.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+528delC | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296163 | |||||||
| chr12:124296164 | C | T | 38 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(35): Show |
40 | HG00323.hp2 HG00673.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.207+528C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296164 | |||||||
| chr12:124296165 | T | C | 9 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(6): Show |
10 | HG01109.hp2 HG01891.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+529T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296165 | |||||||
| chr12:124296166 | C | CTCTCTCT others(32): Show |
6 | a0001c0001t0008g0143 a0001c0001t0008g0147 a0001c0001t0029g0146 others(3): Show |
6 | HG00438.hp2 HG02132.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+531_207+532ins others(39): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296166 | ||||||
| chr12:124296166 | C | CTTTCTCT others(26): Show |
1 | a0001c0001t0008g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.207+532_207+533ins others(33): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296166 | ||||||
| chr12:124296166 | C | CTTTCTTT others(20): Show |
1 | a0001c0001t0008g0134 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.207+532_207+533ins others(27): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296166 | ||||||
| chr12:124296166 | C | T | 331 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(328): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.207+530C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296166 | |||||||
| chr12:124296167 | T | TC | 9 | a0001c0001t0011g0002 a0001c0001t0011g0075 a0001c0002t0002g0068 others(6): Show |
10 | HG01243.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+531_207+532ins others(1): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296167 | |||||||
| chr12:124296167 | T | TCTCTCTT others(70): Show |
1 | a0001c0001t0005g0129 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.207+531_207+532ins others(77): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296167 | |||||||
| chr12:124296167 | T | TCTTTCTT others(102): Show |
2 | a0001c0001t0005g0158 a0001c0001t0005g0159 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.207+531_207+532ins others(109): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296167 | |||||||
| chr12:124296167 | T | TCTTTCTT others(86): Show |
1 | a0001c0001t0034g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.207+531_207+532ins others(93): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296167 | |||||||
| chr12:124296167 | T | TCTTTCTT others(78): Show |
1 | a0001c0001t0032g0189 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.207+531_207+532ins others(85): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296167 | |||||||
| chr12:124296167 | T | TCTTTCTT others(86): Show |
1 | a0001c0001t0005g0161 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.207+531_207+532ins others(93): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296167 | |||||||
| chr12:124296167 | T | TCTTTCTT others(110): Show |
1 | a0001c0001t0005g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.207+531_207+532ins others(117): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296167 | |||||||
| chr12:124296167 | T | TCTTTCTT others(90): Show |
1 | a0001c0001t0005g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.207+531_207+532ins others(97): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296167 | |||||||
| chr12:124296167 | T | TCTTTCTT others(94): Show |
1 | a0001c0001t0005g0191 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.207+531_207+532ins others(101): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296167 | |||||||
| chr12:124296167 | T | TTTCTCTC others(64): Show |
1 | a0001c0001t0013g0124 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.207+532_207+533ins others(71): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296167 | ||||||
| chr12:124296167 | T | TTTCTCTC others(76): Show |
1 | a0001c0001t0005g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.207+532_207+533ins others(83): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296167 | ||||||
| chr12:124296167 | T | TTTCTTTC others(20): Show |
1 | a0001c0001t0011g0057 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.207+532_207+533ins others(27): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296167 | ||||||
| chr12:124296167 | T | TTTCTTTC others(24): Show |
3 | a0001c0001t0011g0051 a0001c0002t0002g0063 a0001c0004t0002g0067 |
3 | HG03471.hp2 HG03942.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.207+532_207+533ins others(31): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296167 | ||||||
| chr12:124296167 | T | TTTCTTTC others(28): Show |
3 | a0001c0002t0002g0049 a0001c0004t0002g0045 a0001c0004t0002g0046 |
3 | HG02109.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.207+532_207+533ins others(35): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296167 | ||||||
| chr12:124296167 | T | TTTCTTTC others(32): Show |
1 | a0001c0004t0002g0048 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.207+532_207+533ins others(39): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296167 | ||||||
| chr12:124296167 | T | TTTCTTTC others(36): Show |
1 | a0001c0001t0011g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.207+532_207+533ins others(43): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296167 | ||||||
| chr12:124296167 | T | TTTCTTTC others(44): Show |
1 | a0001c0001t0005g0258 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.207+532_207+533ins others(51): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296167 | ||||||
| chr12:124296167 | T | TTTCTTTC others(52): Show |
1 | a0001c0001t0001g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.207+532_207+533ins others(59): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296167 | ||||||
| chr12:124296167 | T | TTTCTTTC others(56): Show |
1 | a0001c0001t0001g0356 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.207+532_207+533ins others(63): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296167 | ||||||
| chr12:124296168 | T | C | 2 | a0001c0002t0003g0195 a0001c0002t0003g0220 |
2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.207+532T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296168 | |||||||
| chr12:124296169 | C | T | 3 | a0001c0001t0001g0348 a0001c0002t0003g0195 a0001c0002t0003g0220 |
3 | HG02129.hp2 HG02132.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.207+533C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296169 | |||||||
| chr12:124296171 | C | T | 359 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(356): Show |
367 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.207+535C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296171 | |||||||
| chr12:124296172 | T | TCTTTCTT others(94): Show |
1 | a0001c0002t0002g0248 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.207+536_207+537ins others(101): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296172 | |||||||
| chr12:124296172 | T | TCTTTCTT others(22): Show |
1 | a0001c0004t0002g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.207+536_207+537ins others(29): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296172 | |||||||
| chr12:124296172 | T | TCTTTCTT others(112): Show |
2 | a0001c0002t0002g0152 a0001c0002t0002g0241 |
2 | HG02040.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.207+536_207+537ins others(119): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296172 | |||||||
| chr12:124296173 | T | C | 4 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(1): Show |
5 | HG01109.hp2 HG01891.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+537T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296173 | |||||||
| chr12:124296174 | C | T | 5 | a0001c0001t0001g0348 a0001c0001t0006g0004 a0001c0001t0006g0109 others(2): Show |
6 | HG01109.hp2 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+538C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296174 | |||||||
| chr12:124296176 | C | T | 360 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(357): Show |
368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.207+540C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296176 | |||||||
| chr12:124296181 | C | CCCTCTCT others(138): Show |
1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+545_207+546ins others(145): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296181 | |||||||
| chr12:124296181 | C | CTTCTCTT others(35): Show |
1 | a0004c0008t0035g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.207+549_207+550ins others(42): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296181 | ||||||
| chr12:124296181 | C | CTTTTCTT others(15): Show |
1 | a0001c0001t0005g0246 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.207+547_207+548ins others(22): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296181 | ||||||
| chr12:124296181 | C | T | 361 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(358): Show |
369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.207+545C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296181 | |||||||
| chr12:124296190 | T | TTTCCTTT others(43): Show |
1 | a0001c0002t0007g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.207+556_207+557ins others(50): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTCCTTT others(38): Show |
1 | a0001c0001t0002g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.207+556_207+557ins others(45): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(58): Show |
1 | a0001c0001t0005g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.207+561_207+562ins others(65): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(63): Show |
1 | a0001c0002t0019g0018 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.207+561_207+562ins others(70): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(53): Show |
1 | a0002c0005t0002g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.207+561_207+562ins others(60): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(63): Show |
1 | a0001c0001t0002g0019 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.207+566_207+567ins others(70): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(53): Show |
2 | a0001c0001t0002g0037 a0001c0002t0002g0020 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.207+566_207+567ins others(60): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(48): Show |
2 | a0003c0006t0018g0026 a0003c0006t0018g0033 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.207+566_207+567ins others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(38): Show |
1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+566_207+567ins others(45): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(73): Show |
1 | a0001c0001t0002g0029 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.207+567_207+568ins others(80): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(58): Show |
1 | a0001c0002t0007g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.207+567_207+568ins others(65): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(53): Show |
2 | a0001c0002t0007g0031 a0003c0006t0018g0035 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+567_207+568ins others(60): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(63): Show |
1 | a0001c0001t0002g0030 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.207+567_207+568ins others(70): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(63): Show |
1 | a0001c0001t0002g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.207+567_207+568ins others(70): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(73): Show |
1 | a0001c0001t0002g0034 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.207+567_207+568ins others(80): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(68): Show |
1 | a0001c0001t0013g0024 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.207+567_207+568ins others(75): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(73): Show |
2 | a0001c0001t0002g0021 a0001c0002t0002g0027 |
2 | HG00558.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.207+567_207+568ins others(80): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(78): Show |
2 | a0001c0001t0002g0001 a0001c0001t0033g0032 |
3 | HG01106.hp1 NA18612.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.207+567_207+568ins others(85): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(83): Show |
2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.207+567_207+568ins others(90): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(88): Show |
1 | a0001c0001t0002g0016 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.207+567_207+568ins others(95): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(88): Show |
1 | a0001c0001t0005g0013 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.207+567_207+568ins others(95): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296190 | T | TTTTCTTT others(93): Show |
1 | a0001c0001t0002g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.207+567_207+568ins others(100): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296190 | ||||||
| chr12:124296194 | C | CTT | 249 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(246): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.207+561_207+562dup others(2): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296194 | ||||||
| chr12:124296194 | C | T | 1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+558C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296194 | |||||||
| chr12:124296199 | C | T | 1 | a0001c0002t0002g0097 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.207+563C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296199 | |||||||
| chr12:124296253 | G | C | 4 | a0001c0001t0001g0156 a0001c0002t0004g0263 a0001c0002t0020g0238 others(1): Show |
4 | HG00408.hp2 HG02135.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+617G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296253 | |||||||
| chr12:124296358 | C | G | 13 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(10): Show |
13 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.207+722C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296358 | |||||||
| chr12:124296380 | C | T | 15 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(12): Show |
16 | HG00280.hp1 HG00558.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.207+744C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296380 | |||||||
| chr12:124296400 | C | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0240 a0001c0002t0004g0183 |
3 | HG01192.hp1 HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.207+764C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296400 | |||||||
| chr12:124296405 | G | A | 72 | a0001c0001t0006g0139 a0001c0001t0006g0141 a0001c0001t0006g0148 others(69): Show |
74 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.207+769G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296405 | |||||||
| chr12:124296484 | T | TCCCTGCC others(15): Show |
11 | a0001c0001t0005g0125 a0001c0001t0005g0129 a0001c0001t0005g0158 others(8): Show |
11 | HG01099.hp2 HG02602.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+857_207+878dup others(22): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124296484 | ||||||
| chr12:124296555 | A | G | 1 | a0001c0001t0006g0231 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.207+919A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296555 | |||||||
| chr12:124296655 | C | T | 31 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0011g0002 others(28): Show |
32 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.207+1019C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296655 | |||||||
| chr12:124296722 | G | C | 1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+1086G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296722 | |||||||
| chr12:124296723 | G | T | 1 | a0001c0001t0002g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.207+1087G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296723 | |||||||
| chr12:124296837 | G | T | 1 | a0001c0001t0004g0360 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.207+1201G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296837 | |||||||
| chr12:124296878 | G | A | 1 | a0001c0004t0002g0270 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.207+1242G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296878 | |||||||
| chr12:124296926 | C | T | 4 | a0001c0001t0005g0249 a0001c0002t0002g0152 a0001c0002t0002g0241 others(1): Show |
4 | HG00735.hp2 HG02040.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+1290C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124296926 | |||||||
| chr12:124297146 | T | G | 363 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(360): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.207+1510T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124297146 | |||||||
| chr12:124297237 | C | T | 7 | a0001c0001t0011g0002 a0001c0001t0011g0050 a0001c0001t0011g0051 others(4): Show |
8 | HG02129.hp1 HG03704.hp1 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+1601C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124297237 | |||||||
| chr12:124297246 | C | T | 1 | a0001c0001t0006g0211 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.207+1610C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124297246 | |||||||
| chr12:124297348 | T | A | 1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+1712T>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124297348 | |||||||
| chr12:124297536 | G | A | 1 | a0001c0003t0014g0168 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.207+1900G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124297536 | |||||||
| chr12:124297691 | A | AT | 82 | a0001c0001t0001g0362 a0001c0001t0006g0004 a0001c0001t0006g0109 others(79): Show |
85 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.207+2065dupT | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124297691 | ||||||
| chr12:124297691 | AT | A | 258 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(255): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.207+2065delT | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124297691 | ||||||
| chr12:124297816 | C | G | 4 | a0001c0001t0002g0015 a0001c0001t0005g0246 a0001c0003t0014g0168 others(1): Show |
4 | HG02155.hp1 HG03209.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+2180C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124297816 | |||||||
| chr12:124297917 | C | T | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+2281C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124297917 | |||||||
| chr12:124297918 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0271 |
2 | NA18945.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.207+2282G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124297918 | |||||||
| chr12:124297944 | C | T | 4 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(1): Show |
5 | HG01109.hp2 HG01891.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+2308C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124297944 | |||||||
| chr12:124298275 | C | A | 93 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(90): Show |
96 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.207+2639C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124298275 | |||||||
| chr12:124298276 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.207+2640G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124298276 | |||||||
| chr12:124298381 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.207+2745G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124298381 | |||||||
| chr12:124298512 | G | A | 364 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(361): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.207+2876G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124298512 | |||||||
| chr12:124298627 | C | T | 2 | a0001c0001t0005g0246 a0004c0008t0035g0169 |
2 | HG02155.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.207+2991C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124298627 | |||||||
| chr12:124298697 | C | T | 1 | a0001c0001t0008g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.207+3061C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124298697 | |||||||
| chr12:124298892 | A | G | 1 | a0001c0001t0005g0094 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.207+3256A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124298892 | |||||||
| chr12:124298902 | C | T | 1 | a0001c0002t0004g0272 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.207+3266C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124298902 | |||||||
| chr12:124299194 | C | T | 1 | a0001c0002t0010g0370 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.207+3558C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299194 | |||||||
| chr12:124299195 | G | A | 2 | a0001c0001t0033g0032 a0001c0002t0002g0027 |
2 | HG00558.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.207+3559G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299195 | |||||||
| chr12:124299260 | C | T | 234 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(231): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.207+3624C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299260 | |||||||
| chr12:124299411 | T | G | 90 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0246 others(87): Show |
93 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.207+3775T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299411 | |||||||
| chr12:124299412 | C | A | 90 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0246 others(87): Show |
93 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.207+3776C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299412 | |||||||
| chr12:124299414 | A | G | 90 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0246 others(87): Show |
93 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.207+3778A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299414 | |||||||
| chr12:124299415 | T | C | 90 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0246 others(87): Show |
93 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.207+3779T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299415 | |||||||
| chr12:124299426 | C | T | 90 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0246 others(87): Show |
93 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.207+3790C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299426 | |||||||
| chr12:124299429 | T | C | 106 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(103): Show |
110 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.207+3793T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299429 | |||||||
| chr12:124299435 | G | A | 90 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0246 others(87): Show |
93 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.207+3799G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299435 | |||||||
| chr12:124299440 | T | G | 90 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0246 others(87): Show |
93 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.207+3804T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299440 | |||||||
| chr12:124299651 | A | G | 16 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(13): Show |
17 | HG00280.hp1 HG00558.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.207+4015A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299651 | |||||||
| chr12:124299790 | G | A | 20 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0246 others(17): Show |
20 | HG00735.hp2 HG02040.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.207+4154G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299790 | |||||||
| chr12:124299810 | C | CTGAGCAG others(6): Show |
49 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0056 others(46): Show |
50 | HG00735.hp2 HG01099.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.207+4176_207+4177i others(15): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124299810 | ||||||
| chr12:124299850 | G | A | 5 | a0001c0001t0005g0246 a0001c0003t0014g0069 a0001c0003t0014g0072 others(2): Show |
5 | HG02155.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+4214G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299850 | |||||||
| chr12:124299861 | T | C | 1 | a0001c0001t0005g0103 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.207+4225T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299861 | |||||||
| chr12:124299868 | A | G | 1 | a0001c0002t0004g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.207+4232A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299868 | |||||||
| chr12:124299895 | C | T | 234 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(231): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.207+4259C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299895 | |||||||
| chr12:124299937 | G | A | 29 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0011g0002 others(26): Show |
30 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.207+4301G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299937 | |||||||
| chr12:124299957 | T | C | 1 | a0001c0001t0011g0057 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.207+4321T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124299957 | |||||||
| chr12:124300016 | A | G | 5 | a0001c0001t0005g0246 a0001c0003t0014g0069 a0001c0003t0014g0072 others(2): Show |
5 | HG02155.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+4380A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300016 | |||||||
| chr12:124300060 | A | C | 234 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(231): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.207+4424A>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300060 | |||||||
| chr12:124300164 | G | A | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+4528G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300164 | |||||||
| chr12:124300464 | C | G | 1 | a0001c0002t0003g0212 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.207+4828C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300464 | |||||||
| chr12:124300544 | T | A | 11 | a0001c0001t0005g0249 a0001c0001t0013g0126 a0001c0002t0002g0152 others(8): Show |
11 | HG00735.hp2 HG02040.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+4908T>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300544 | |||||||
| chr12:124300552 | G | A | 234 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(231): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.207+4916G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300552 | |||||||
| chr12:124300561 | A | AGGAT | 85 | a0001c0001t0005g0094 a0001c0001t0006g0004 a0001c0001t0006g0109 others(82): Show |
88 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.207+4946_207+4949d others(6): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300561 | ||||||
| chr12:124300592 | A | ATGGATGG others(25): Show |
2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.207+4977_207+5008d others(34): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300592 | ||||||
| chr12:124300687 | AATAG | A | 11 | a0001c0001t0005g0249 a0001c0001t0013g0126 a0001c0002t0002g0152 others(8): Show |
11 | HG00735.hp2 HG02040.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+5057_207+5060d others(6): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300687 | ||||||
| chr12:124300720 | GTGGATGG others(5): Show |
G | 8 | a0001c0001t0005g0249 a0001c0001t0013g0126 a0001c0002t0002g0152 others(5): Show |
8 | HG00735.hp2 HG02040.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+5095_207+5106d others(14): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300720 | ||||||
| chr12:124300720 | GTGGATGG others(9): Show |
G | 2 | a0001c0003t0014g0153 a0001c0003t0014g0185 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.207+5095_207+5110d others(18): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300720 | ||||||
| chr12:124300731 | C | G | 7 | a0001c0001t0005g0246 a0001c0001t0008g0134 a0001c0001t0008g0167 others(4): Show |
7 | HG02155.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+5095C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300731 | |||||||
| chr12:124300731 | CATGG | C | 7 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(4): Show |
8 | HG01109.hp2 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+5134_207+5137d others(6): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300731 | ||||||
| chr12:124300731 | CATGGATG others(1): Show |
C | 6 | a0001c0001t0008g0113 a0001c0001t0008g0114 a0001c0001t0008g0115 others(3): Show |
6 | HG00735.hp1 HG01361.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+5130_207+5137d others(10): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300731 | ||||||
| chr12:124300731 | CATGGATG others(5): Show |
C | 162 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0039 others(159): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.207+5126_207+5137d others(14): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300731 | ||||||
| chr12:124300733 | TGGATGGA others(6): Show |
T | 1 | a0001c0002t0002g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.207+5099_207+5111d others(15): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300733 | ||||||
| chr12:124300737 | TGGATGGA others(33): Show |
T | 1 | a0001c0001t0002g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.207+5138_207+5177d others(42): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300737 | ||||||
| chr12:124300741 | TGGATGGA others(29): Show |
T | 1 | a0001c0001t0002g0131 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.207+5138_207+5173d others(38): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300741 | ||||||
| chr12:124300749 | TGGATGGA others(21): Show |
T | 1 | a0001c0001t0001g0267 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.207+5138_207+5165d others(30): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300749 | ||||||
| chr12:124300750 | G | T | 5 | a0001c0001t0005g0246 a0001c0003t0014g0069 a0001c0003t0014g0072 others(2): Show |
5 | HG02155.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+5114G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300750 | |||||||
| chr12:124300753 | T | C | 5 | a0001c0001t0005g0246 a0001c0003t0014g0069 a0001c0003t0014g0072 others(2): Show |
5 | HG02155.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+5117T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300753 | |||||||
| chr12:124300757 | TGGATGGA others(13): Show |
T | 5 | a0001c0001t0005g0246 a0001c0003t0014g0069 a0001c0003t0014g0072 others(2): Show |
5 | HG02155.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+5138_207+5157d others(22): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300757 | ||||||
| chr12:124300762 | G | T | 69 | a0001c0001t0001g0009 a0001c0001t0001g0243 a0001c0001t0001g0244 others(66): Show |
71 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.207+5126G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300762 | |||||||
| chr12:124300765 | T | C | 69 | a0001c0001t0001g0009 a0001c0001t0001g0243 a0001c0001t0001g0244 others(66): Show |
71 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.207+5129T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300765 | |||||||
| chr12:124300766 | G | T | 1 | a0001c0002t0002g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.207+5130G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300766 | |||||||
| chr12:124300769 | T | C | 1 | a0001c0002t0002g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.207+5133T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300769 | |||||||
| chr12:124300769 | TGGATTGA others(1): Show |
T | 59 | a0001c0001t0001g0009 a0001c0001t0001g0243 a0001c0001t0001g0244 others(56): Show |
61 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.207+5138_207+5145d others(10): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300769 | ||||||
| chr12:124300773 | TTGAC | T | 15 | a0001c0001t0001g0298 a0001c0001t0001g0317 a0001c0001t0001g0348 others(12): Show |
15 | HG00323.hp2 HG00642.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+5138_207+5141d others(6): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300773 | |||||||
| chr12:124300774 | T | G | 1 | a0001c0001t0008g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.207+5138T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300774 | |||||||
| chr12:124300777 | C | T | 1 | a0001c0001t0008g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.207+5141C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300777 | |||||||
| chr12:124300777 | CGGAT | C | 46 | a0001c0001t0001g0156 a0001c0001t0001g0240 a0001c0001t0005g0056 others(43): Show |
47 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.207+5177_207+5180d others(6): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300777 | ||||||
| chr12:124300777 | CGGATGGA others(1): Show |
C | 76 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(73): Show |
79 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.207+5173_207+5180d others(10): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300777 | ||||||
| chr12:124300777 | CGGATGGA others(9): Show |
C | 1 | a0001c0002t0003g0208 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.207+5165_207+5180d others(18): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300777 | ||||||
| chr12:124300782 | G | T | 5 | a0001c0001t0006g0141 a0001c0001t0006g0178 a0001c0001t0008g0167 others(2): Show |
5 | HG00323.hp2 HG00642.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+5146G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300782 | |||||||
| chr12:124300785 | T | C | 5 | a0001c0001t0006g0141 a0001c0001t0006g0178 a0001c0001t0008g0167 others(2): Show |
5 | HG00323.hp2 HG00642.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+5149T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300785 | |||||||
| chr12:124300790 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.207+5154G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300790 | |||||||
| chr12:124300793 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.207+5157T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300793 | |||||||
| chr12:124300800 | A | ATGGATGG others(21): Show |
1 | a0001c0003t0009g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.207+5209_207+5236d others(30): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300800 | ||||||
| chr12:124300916 | G | A | 1 | a0001c0002t0007g0083 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.207+5280G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300916 | |||||||
| chr12:124300916 | G | GTGGA | 119 | a0001c0001t0005g0094 a0001c0001t0005g0102 a0001c0001t0005g0103 others(116): Show |
123 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.207+5305_207+5308d others(6): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300916 | ||||||
| chr12:124300916 | G | GTGGATGG others(1): Show |
3 | a0001c0001t0005g0246 a0001c0001t0006g0112 a0004c0008t0035g0169 |
3 | HG01109.hp2 HG02155.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.207+5301_207+5308d others(10): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124300916 | ||||||
| chr12:124300998 | A | G | 80 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(77): Show |
83 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.207+5362A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124300998 | |||||||
| chr12:124301004 | T | G | 1 | a0001c0001t0024g0239 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.207+5368T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301004 | |||||||
| chr12:124301113 | C | A | 80 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(77): Show |
83 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.207+5477C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301113 | |||||||
| chr12:124301212 | C | T | 1 | a0001c0002t0007g0372 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.207+5576C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301212 | |||||||
| chr12:124301234 | G | A | 1 | a0001c0007t0002g0098 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.207+5598G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301234 | |||||||
| chr12:124301236 | G | C | 26 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0011g0002 others(23): Show |
27 | HG01099.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.207+5600G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301236 | |||||||
| chr12:124301471 | T | A | 234 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(231): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.207+5835T>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301471 | |||||||
| chr12:124301507 | C | T | 234 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(231): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.207+5871C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301507 | |||||||
| chr12:124301508 | G | A | 3 | a0001c0003t0014g0069 a0001c0003t0014g0072 a0001c0003t0014g0168 |
3 | HG02615.hp1 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.207+5872G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301508 | |||||||
| chr12:124301542 | G | A | 80 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(77): Show |
83 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.207+5906G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301542 | |||||||
| chr12:124301551 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.207+5915G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301551 | |||||||
| chr12:124301607 | C | T | 1 | a0001c0002t0004g0376 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.207+5971C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301607 | |||||||
| chr12:124301638 | C | CG | 3 | a0001c0001t0006g0205 a0001c0002t0003g0166 a0001c0002t0003g0236 |
3 | NA18981.hp2 NA19011.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.207+6002_207+6003i others(3): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301638 | |||||||
| chr12:124301639 | A | G | 77 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(74): Show |
80 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.207+6003A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301639 | |||||||
| chr12:124301639 | A | T | 3 | a0001c0001t0006g0205 a0001c0002t0003g0166 a0001c0002t0003g0236 |
3 | NA18981.hp2 NA19011.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.207+6003A>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301639 | |||||||
| chr12:124301686 | G | A | 1 | a0001c0002t0027g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.207+6050G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301686 | |||||||
| chr12:124301945 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(23): Show |
27 | HG00280.hp1 HG00558.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.207+6309G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301945 | |||||||
| chr12:124301963 | C | T | 28 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0011g0002 others(25): Show |
29 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+6327C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301963 | |||||||
| chr12:124301964 | G | A | 1 | a0001c0001t0006g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.207+6328G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124301964 | |||||||
| chr12:124302191 | A | T | 1 | a0001c0001t0001g0366 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.207+6555A>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302191 | |||||||
| chr12:124302241 | G | A | 13 | a0001c0001t0005g0249 a0001c0001t0013g0126 a0001c0002t0002g0152 others(10): Show |
13 | HG00735.hp2 HG02040.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.207+6605G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302241 | |||||||
| chr12:124302339 | G | A | 4 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(1): Show |
5 | HG01109.hp2 HG01891.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+6703G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302339 | |||||||
| chr12:124302341 | C | A | 1 | a0001c0003t0009g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.207+6705C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302341 | |||||||
| chr12:124302435 | T | G | 1 | a0001c0002t0017g0260 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.207+6799T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302435 | |||||||
| chr12:124302443 | C | T | 364 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(361): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.207+6807C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302443 | |||||||
| chr12:124302550 | C | A | 1 | a0001c0001t0001g0365 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.207+6914C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302550 | |||||||
| chr12:124302555 | C | G | 364 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(361): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.207+6919C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302555 | |||||||
| chr12:124302651 | C | T | 364 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(361): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.207+7015C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302651 | |||||||
| chr12:124302685 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.207+7049C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302685 | |||||||
| chr12:124302790 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.207+7154G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302790 | |||||||
| chr12:124302805 | T | C | 316 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(313): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.207+7169T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302805 | |||||||
| chr12:124302813 | G | GGGGCCGA others(7): Show |
79 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(76): Show |
82 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.207+7190_207+7191i others(16): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124302813 | ||||||
| chr12:124302813 | G | GGGGCCGA others(20): Show |
10 | a0001c0001t0001g0342 a0001c0001t0005g0246 a0001c0001t0015g0337 others(7): Show |
10 | HG00621.hp1 HG02004.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+7204_207+7230d others(29): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124302813 | ||||||
| chr12:124302813 | G | GGGGCCGA others(46): Show |
1 | a0001c0003t0014g0168 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.207+7194_207+7195i others(55): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124302813 | ||||||
| chr12:124302813 | GGGGCCGA others(20): Show |
G | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+7204_207+7230d others(29): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124302813 | ||||||
| chr12:124302826 | G | GAGGGCCG others(21): Show |
54 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(51): Show |
55 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.207+7190_207+7191i others(30): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302826 | |||||||
| chr12:124302826 | G | GGGGGCCG others(21): Show |
1 | a0001c0001t0005g0104 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.207+7193_207+7194i others(30): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124302826 | ||||||
| chr12:124302839 | GA | G | 55 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(52): Show |
56 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.207+7204delA | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302839 | |||||||
| chr12:124302840 | A | AGGGCCGA others(6): Show |
2 | a0001c0001t0001g0333 a0001c0001t0001g0368 |
2 | HG01515.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.207+7234_207+7246d others(15): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124302840 | ||||||
| chr12:124302840 | A | AGGGCCGA others(33): Show |
156 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(153): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.207+7230_207+7231i others(42): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124302840 | ||||||
| chr12:124302840 | A | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0030 |
2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.207+7204A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302840 | |||||||
| chr12:124302846 | G | A | 3 | a0001c0002t0002g0074 a0001c0002t0022g0053 a0001c0002t0022g0071 |
3 | HG01243.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.207+7210G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302846 | |||||||
| chr12:124302853 | G | GGGGCCGA others(60): Show |
2 | a0001c0001t0002g0021 a0001c0001t0002g0030 |
2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.207+7246_207+7247i others(69): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124302853 | ||||||
| chr12:124302853 | G | GGGGGCCG others(61): Show |
2 | a0001c0001t0033g0032 a0001c0002t0002g0027 |
2 | HG00558.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.207+7220_207+7221i others(70): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124302853 | ||||||
| chr12:124302853 | G | GGGGGCCG others(74): Show |
12 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(9): Show |
13 | HG00280.hp1 HG01106.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.207+7220_207+7221i others(83): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124302853 | ||||||
| chr12:124302929 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.207+7293G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302929 | |||||||
| chr12:124302985 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.207+7349A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302985 | |||||||
| chr12:124302993 | C | G | 220 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(217): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.207+7357C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302993 | |||||||
| chr12:124302994 | T | C | 5 | a0001c0001t0005g0246 a0001c0003t0014g0069 a0001c0003t0014g0072 others(2): Show |
5 | HG02155.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+7358T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124302994 | |||||||
| chr12:124303146 | G | A | 228 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(225): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.207+7510G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303146 | |||||||
| chr12:124303275 | G | A | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+7639G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303275 | |||||||
| chr12:124303309 | G | A | 1 | a0004c0008t0035g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.207+7673G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303309 | |||||||
| chr12:124303428 | C | G | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+7792C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303428 | |||||||
| chr12:124303535 | C | G | 4 | a0001c0001t0005g0249 a0001c0002t0002g0152 a0001c0002t0002g0241 others(1): Show |
4 | HG00735.hp2 HG02040.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+7899C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303535 | |||||||
| chr12:124303591 | C | T | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+7955C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303591 | |||||||
| chr12:124303754 | C | G | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-8064C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303754 | |||||||
| chr12:124303755 | C | T | 4 | a0001c0001t0013g0250 a0001c0002t0002g0020 a0001c0002t0002g0251 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-8063C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303755 | |||||||
| chr12:124303778 | C | T | 1 | a0001c0001t0011g0057 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.208-8040C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303778 | |||||||
| chr12:124303806 | C | A | 80 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(77): Show |
83 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.208-8012C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303806 | |||||||
| chr12:124303815 | G | T | 1 | a0001c0001t0006g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.208-8003G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303815 | |||||||
| chr12:124303886 | C | G | 2 | a0001c0001t0008g0147 a0001c0001t0008g0217 |
2 | HG02132.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.208-7932C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303886 | |||||||
| chr12:124303950 | T | C | 364 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(361): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.208-7868T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303950 | |||||||
| chr12:124303988 | C | T | 5 | a0001c0001t0005g0102 a0001c0002t0002g0082 a0001c0002t0002g0093 others(2): Show |
5 | HG01346.hp2 HG01928.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-7830C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124303988 | |||||||
| chr12:124304032 | G | A | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-7786G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304032 | |||||||
| chr12:124304148 | T | C | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-7670T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304148 | |||||||
| chr12:124304166 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.208-7652G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304166 | |||||||
| chr12:124304245 | C | T | 4 | a0001c0003t0014g0069 a0001c0003t0014g0072 a0001c0003t0014g0168 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-7573C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304245 | |||||||
| chr12:124304247 | C | T | 3 | a0001c0002t0017g0257 a0001c0002t0017g0260 a0001c0002t0017g0261 |
3 | HG02647.hp2 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.208-7571C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304247 | |||||||
| chr12:124304310 | G | A | 2 | a0001c0001t0011g0050 a0001c0001t0011g0051 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.208-7508G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304310 | |||||||
| chr12:124304361 | C | T | 1 | a0004c0008t0035g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.208-7457C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304361 | |||||||
| chr12:124304438 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.208-7380C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304438 | |||||||
| chr12:124304500 | C | T | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-7318C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304500 | |||||||
| chr12:124304543 | T | C | 364 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(361): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.208-7275T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304543 | |||||||
| chr12:124304551 | G | A | 4 | a0001c0003t0014g0069 a0001c0003t0014g0072 a0001c0003t0014g0168 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-7267G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304551 | |||||||
| chr12:124304608 | G | A | 2 | a0001c0001t0005g0190 a0001c0001t0005g0200 |
2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.208-7210G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304608 | |||||||
| chr12:124304732 | C | G | 4 | a0001c0001t0005g0125 a0001c0001t0005g0158 a0001c0001t0005g0159 others(1): Show |
4 | HG02738.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-7086C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304732 | |||||||
| chr12:124304771 | C | G | 1 | a0001c0001t0001g0354 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.208-7047C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304771 | |||||||
| chr12:124304776 | C | T | 1 | a0001c0001t0013g0024 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208-7042C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304776 | |||||||
| chr12:124304784 | T | C | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-7034T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304784 | |||||||
| chr12:124304818 | C | T | 7 | a0001c0002t0002g0068 a0001c0002t0007g0052 a0001c0002t0030g0011 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-7000C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304818 | |||||||
| chr12:124304936 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.208-6882C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304936 | |||||||
| chr12:124304961 | C | T | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-6857C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124304961 | |||||||
| chr12:124304987 | AGT | A | 15 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0021g0059 others(12): Show |
15 | HG01099.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.208-6826_208-6825d others(4): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124304987 | ||||||
| chr12:124305004 | A | G | 364 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(361): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.208-6814A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305004 | |||||||
| chr12:124305021 | A | G | 4 | a0001c0003t0014g0069 a0001c0003t0014g0072 a0001c0003t0014g0168 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-6797A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305021 | |||||||
| chr12:124305183 | C | T | 12 | a0001c0001t0005g0028 a0001c0001t0005g0249 a0001c0001t0013g0126 others(9): Show |
12 | HG00735.hp2 HG01943.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.208-6635C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305183 | |||||||
| chr12:124305242 | C | T | 233 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(230): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.208-6576C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305242 | |||||||
| chr12:124305268 | C | T | 10 | a0001c0001t0001g0181 a0001c0001t0001g0254 a0001c0001t0001g0256 others(7): Show |
10 | HG01884.hp2 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.208-6550C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305268 | |||||||
| chr12:124305286 | C | G | 81 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(78): Show |
84 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.208-6532C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305286 | |||||||
| chr12:124305324 | G | A | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-6494G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305324 | |||||||
| chr12:124305331 | G | GGGAGGCG others(6): Show |
1 | a0001c0001t0011g0075 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.208-6486_208-6474d others(15): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124305331 | ||||||
| chr12:124305362 | G | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.208-6456G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305362 | |||||||
| chr12:124305479 | C | T | 233 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(230): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.208-6339C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305479 | |||||||
| chr12:124305606 | C | G | 2 | a0001c0001t0001g0324 a0001c0001t0001g0328 |
2 | HG01256.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.208-6212C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305606 | |||||||
| chr12:124305607 | C | T | 6 | a0001c0002t0002g0079 a0001c0002t0002g0081 a0001c0002t0002g0084 others(3): Show |
6 | NA18940.hp2 NA18944.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-6211C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305607 | |||||||
| chr12:124305636 | C | G | 97 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0028 others(94): Show |
100 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208-6182C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305636 | |||||||
| chr12:124305648 | G | A | 39 | a0001c0001t0005g0094 a0001c0001t0005g0102 a0001c0001t0005g0103 others(36): Show |
40 | HG01070.hp1 HG01071.hp1 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.208-6170G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305648 | |||||||
| chr12:124305695 | A | C | 131 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0005g0028 others(128): Show |
135 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.208-6123A>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305695 | |||||||
| chr12:124305746 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0271 a0001c0001t0001g0339 |
3 | HG02074.hp1 NA18945.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.208-6072C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305746 | |||||||
| chr12:124305757 | A | G | 4 | a0001c0001t0006g0226 a0001c0001t0013g0090 a0001c0002t0010g0180 others(1): Show |
4 | NA18947.hp2 NA18950.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-6061A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305757 | |||||||
| chr12:124305791 | C | T | 1 | a0001c0001t0008g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.208-6027C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305791 | |||||||
| chr12:124305842 | G | T | 1 | a0001c0003t0009g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.208-5976G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305842 | |||||||
| chr12:124305843 | C | G | 1 | a0001c0003t0009g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.208-5975C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305843 | |||||||
| chr12:124305881 | C | T | 4 | a0001c0003t0014g0069 a0001c0003t0014g0072 a0001c0003t0014g0168 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-5937C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305881 | |||||||
| chr12:124305922 | C | T | 1 | a0001c0001t0029g0146 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.208-5896C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305922 | |||||||
| chr12:124305971 | C | T | 233 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(230): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.208-5847C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124305971 | |||||||
| chr12:124306010 | G | A | 2 | a0001c0004t0002g0061 a0001c0004t0002g0270 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208-5808G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306010 | |||||||
| chr12:124306013 | C | T | 1 | a0001c0001t0001g0355 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.208-5805C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306013 | |||||||
| chr12:124306119 | G | A | 163 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(160): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.208-5699G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306119 | |||||||
| chr12:124306150 | C | T | 27 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0011g0002 others(24): Show |
28 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.208-5668C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306150 | |||||||
| chr12:124306228 | G | A | 27 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0011g0002 others(24): Show |
28 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.208-5590G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306228 | |||||||
| chr12:124306259 | G | A | 1 | a0001c0007t0002g0098 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.208-5559G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306259 | |||||||
| chr12:124306468 | G | A | 1 | a0001c0001t0025g0280 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.208-5350G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306468 | |||||||
| chr12:124306534 | C | T | 1 | a0004c0008t0035g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.208-5284C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306534 | |||||||
| chr12:124306668 | C | A | 39 | a0001c0001t0005g0094 a0001c0001t0005g0102 a0001c0001t0005g0103 others(36): Show |
40 | HG01070.hp1 HG01071.hp1 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.208-5150C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306668 | |||||||
| chr12:124306723 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.208-5095G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306723 | |||||||
| chr12:124306937 | T | C | 9 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0021g0059 others(6): Show |
9 | HG01099.hp1 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-4881T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124306937 | |||||||
| chr12:124307012 | C | T | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.208-4806C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307012 | |||||||
| chr12:124307098 | C | G | 168 | a0001c0001t0001g0317 a0001c0001t0002g0130 a0001c0001t0002g0131 others(165): Show |
173 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.208-4720C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307098 | |||||||
| chr12:124307104 | G | T | 129 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(126): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.208-4714G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307104 | |||||||
| chr12:124307160 | G | A | 4 | a0001c0003t0014g0069 a0001c0003t0014g0072 a0001c0003t0014g0168 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-4658G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307160 | |||||||
| chr12:124307252 | C | T | 27 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0011g0002 others(24): Show |
28 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.208-4566C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307252 | |||||||
| chr12:124307382 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.208-4436C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307382 | |||||||
| chr12:124307488 | A | C | 1 | a0001c0002t0002g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.208-4330A>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307488 | |||||||
| chr12:124307496 | C | T | 3 | a0001c0002t0017g0257 a0001c0002t0017g0260 a0001c0002t0017g0261 |
3 | HG02647.hp2 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.208-4322C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307496 | |||||||
| chr12:124307499 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0286 |
2 | HG01167.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.208-4319C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307499 | |||||||
| chr12:124307525 | G | A | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-4293G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307525 | |||||||
| chr12:124307535 | C | T | 1 | a0001c0001t0005g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.208-4283C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307535 | |||||||
| chr12:124307669 | G | T | 40 | a0001c0001t0005g0094 a0001c0001t0005g0102 a0001c0001t0005g0103 others(37): Show |
41 | HG01070.hp1 HG01071.hp1 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.208-4149G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307669 | |||||||
| chr12:124307679 | C | T | 6 | a0001c0001t0005g0028 a0001c0001t0005g0249 a0001c0001t0013g0126 others(3): Show |
6 | HG00735.hp2 HG01943.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-4139C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307679 | |||||||
| chr12:124307727 | T | G | 10 | a0001c0001t0001g0346 a0001c0001t0001g0358 a0001c0001t0001g0361 others(7): Show |
10 | HG01074.hp2 HG01361.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-4091T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307727 | |||||||
| chr12:124307793 | C | G | 1 | a0001c0001t0001g0322 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.208-4025C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307793 | |||||||
| chr12:124307803 | G | T | 1 | a0001c0002t0003g0216 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.208-4015G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307803 | |||||||
| chr12:124307851 | A | G | 6 | a0001c0002t0007g0372 a0001c0002t0019g0182 a0001c0002t0019g0186 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-3967A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307851 | |||||||
| chr12:124307898 | T | A | 1 | a0001c0001t0011g0070 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.208-3920T>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307898 | |||||||
| chr12:124307905 | G | A | 38 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0181 others(35): Show |
38 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.208-3913G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307905 | |||||||
| chr12:124307936 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.208-3882C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307936 | |||||||
| chr12:124307969 | C | T | 2 | a0001c0002t0019g0182 a0001c0002t0019g0186 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.208-3849C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124307969 | |||||||
| chr12:124307983 | C | CT | 83 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0181 others(80): Show |
84 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.208-3819dupT | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124307983 | ||||||
| chr12:124307983 | CT | C | 16 | a0001c0001t0001g0367 a0001c0001t0006g0148 a0001c0001t0006g0165 others(13): Show |
16 | HG01517.hp1 HG03688.hp1 NA18943.hp1 others(13): Show |
intron_variant | MODIFIER | c.208-3819delT | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124307983 | ||||||
| chr12:124308012 | C | T | 1 | a0004c0008t0035g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.208-3806C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308012 | |||||||
| chr12:124308069 | C | T | 1 | a0001c0002t0004g0259 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.208-3749C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308069 | |||||||
| chr12:124308102 | G | C | 144 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(141): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.208-3716G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308102 | |||||||
| chr12:124308126 | C | T | 37 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0181 others(34): Show |
37 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.208-3692C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308126 | |||||||
| chr12:124308349 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.208-3469C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308349 | |||||||
| chr12:124308416 | C | T | 1 | a0001c0002t0007g0201 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208-3402C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308416 | |||||||
| chr12:124308433 | G | C | 6 | a0001c0001t0005g0028 a0001c0001t0005g0249 a0001c0001t0013g0126 others(3): Show |
6 | HG00735.hp2 HG01943.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-3385G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308433 | |||||||
| chr12:124308457 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.208-3361C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308457 | |||||||
| chr12:124308460 | C | CG | 19 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0011g0002 others(16): Show |
20 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.208-3358_208-3357i others(3): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308460 | |||||||
| chr12:124308461 | C | G | 45 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0181 others(42): Show |
45 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.208-3357C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308461 | |||||||
| chr12:124308462 | C | T | 19 | a0001c0001t0005g0056 a0001c0001t0005g0058 a0001c0001t0011g0002 others(16): Show |
20 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.208-3356C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308462 | |||||||
| chr12:124308465 | G | T | 1 | a0001c0002t0002g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.208-3353G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308465 | |||||||
| chr12:124308466 | T | G | 1 | a0001c0002t0002g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.208-3352T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308466 | |||||||
| chr12:124308467 | C | T | 1 | a0001c0002t0002g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.208-3351C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308467 | |||||||
| chr12:124308503 | C | T | 15 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(12): Show |
16 | HG00280.hp1 HG00558.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.208-3315C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308503 | |||||||
| chr12:124308694 | G | C | 1 | a0001c0002t0003g0223 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.208-3124G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308694 | |||||||
| chr12:124308741 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0001g0328 |
2 | HG01256.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.208-3077G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308741 | |||||||
| chr12:124308954 | G | A | 3 | a0001c0003t0014g0069 a0001c0003t0014g0072 a0001c0003t0014g0168 |
3 | HG02615.hp1 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.208-2864G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308954 | |||||||
| chr12:124308983 | C | A | 1 | a0001c0001t0008g0217 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.208-2835C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124308983 | |||||||
| chr12:124309019 | C | T | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-2799C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309019 | |||||||
| chr12:124309049 | C | T | 1 | a0001c0002t0030g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208-2769C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309049 | |||||||
| chr12:124309093 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.208-2725C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309093 | |||||||
| chr12:124309148 | G | T | 4 | a0001c0003t0014g0069 a0001c0003t0014g0072 a0001c0003t0014g0168 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-2670G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309148 | |||||||
| chr12:124309273 | C | A | 1 | a0001c0001t0001g0348 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.208-2545C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309273 | |||||||
| chr12:124309274 | C | A | 1 | a0001c0001t0002g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.208-2544C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309274 | |||||||
| chr12:124309276 | T | C | 1 | a0001c0001t0001g0348 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.208-2542T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309276 | |||||||
| chr12:124309387 | G | A | 1 | a0001c0001t0006g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.208-2431G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309387 | |||||||
| chr12:124309395 | G | C | 1 | a0001c0001t0006g0170 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.208-2423G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309395 | |||||||
| chr12:124309423 | A | G | 1 | a0001c0001t0005g0028 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.208-2395A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309423 | |||||||
| chr12:124309433 | G | T | 1 | a0002c0005t0005g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.208-2385G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309433 | |||||||
| chr12:124309581 | A | G | 1 | a0001c0001t0001g0309 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.208-2237A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309581 | |||||||
| chr12:124309634 | T | G | 6 | a0001c0002t0002g0074 a0001c0002t0017g0257 a0001c0002t0017g0260 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-2184T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309634 | |||||||
| chr12:124309651 | C | T | 1 | a0001c0002t0019g0018 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.208-2167C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309651 | |||||||
| chr12:124309725 | T | C | 134 | a0001c0001t0001g0336 a0001c0001t0001g0348 a0001c0001t0002g0036 others(131): Show |
136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.208-2093T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309725 | |||||||
| chr12:124309734 | A | G | 128 | a0001c0001t0001g0336 a0001c0001t0001g0348 a0001c0001t0002g0036 others(125): Show |
130 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.208-2084A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309734 | |||||||
| chr12:124309893 | G | A | 4 | a0001c0001t0005g0129 a0001c0001t0013g0124 a0001c0001t0024g0239 others(1): Show |
4 | HG01099.hp2 HG02602.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-1925G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124309893 | |||||||
| chr12:124310116 | T | G | 1 | a0001c0001t0001g0311 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.208-1702T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310116 | |||||||
| chr12:124310136 | G | A | 1 | a0001c0001t0025g0280 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.208-1682G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310136 | |||||||
| chr12:124310165 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.208-1653T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310165 | |||||||
| chr12:124310172 | C | CA | 9 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(6): Show |
10 | HG00280.hp1 HG01106.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-1622dupA | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAA | 18 | a0001c0001t0006g0226 a0001c0002t0002g0082 a0001c0002t0007g0003 others(15): Show |
19 | HG01070.hp1 HG01071.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.208-1625_208-1622d others(6): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAA | 11 | a0001c0001t0006g0205 a0001c0001t0006g0232 a0001c0001t0013g0090 others(8): Show |
11 | HG02055.hp1 HG02056.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.208-1626_208-1622d others(7): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAA | 26 | a0001c0001t0001g0181 a0001c0001t0001g0240 a0001c0001t0001g0256 others(23): Show |
26 | HG00140.hp1 HG00642.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.208-1627_208-1622d others(8): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA | 9 | a0001c0001t0001g0254 a0001c0001t0002g0022 a0001c0001t0002g0131 others(6): Show |
10 | HG01884.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.208-1628_208-1622d others(9): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0003g0210 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.208-1631_208-1622d others(12): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0302 a0001c0002t0004g0293 |
2 | HG02735.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.208-1632_208-1622d others(13): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(5): Show |
2 | a0001c0002t0002g0095 a0001c0002t0007g0372 |
2 | HG02622.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.208-1633_208-1622d others(14): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(6): Show |
3 | a0001c0002t0002g0091 a0001c0002t0031g0371 a0001c0003t0014g0069 |
3 | HG02615.hp1 HG03195.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.208-1634_208-1622d others(15): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0002t0002g0084 others(2): Show |
5 | HG02818.hp1 NA18982.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.208-1635_208-1622d others(16): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(8): Show |
44 | a0001c0001t0008g0118 a0001c0001t0008g0143 a0001c0001t0008g0147 others(41): Show |
45 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.208-1636_208-1622d others(17): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(9): Show |
41 | a0001c0001t0005g0103 a0001c0001t0013g0250 a0001c0001t0029g0146 others(38): Show |
42 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.208-1637_208-1622d others(18): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(10): Show |
14 | a0001c0001t0001g0199 a0001c0001t0001g0323 a0001c0001t0001g0348 others(11): Show |
14 | HG01167.hp1 HG01943.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.208-1638_208-1622d others(19): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(11): Show |
42 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0156 others(39): Show |
43 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.208-1639_208-1622d others(20): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(12): Show |
45 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
46 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.208-1640_208-1622d others(21): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(13): Show |
23 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0157 others(20): Show |
23 | HG01099.hp1 HG01952.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.208-1641_208-1622d others(22): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(14): Show |
7 | a0001c0001t0001g0277 a0001c0001t0001g0312 a0001c0001t0001g0324 others(4): Show |
7 | HG01255.hp2 HG01256.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-1642_208-1622d others(23): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(15): Show |
6 | a0001c0001t0001g0242 a0001c0001t0001g0284 a0001c0001t0005g0056 others(3): Show |
6 | HG00639.hp1 HG01071.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-1643_208-1622d others(24): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0282 a0001c0001t0001g0352 a0001c0001t0005g0249 |
3 | HG00140.hp2 HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.208-1644_208-1622d others(25): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0364 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.208-1645_208-1622d others(26): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0326 a0002c0005t0005g0054 |
2 | HG02258.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.208-1622_208-1621i others(27): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | C | CAAAAAAA others(20): Show |
1 | a0002c0005t0005g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.208-1622_208-1621i others(29): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | CA | C | 20 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0191 others(17): Show |
21 | HG02027.hp1 HG02109.hp1 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.208-1622delA | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310172 | CAA | C | 8 | a0001c0002t0002g0049 a0001c0002t0017g0257 a0001c0002t0017g0260 others(5): Show |
8 | HG01243.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.208-1623_208-1622d others(4): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310172 | ||||||
| chr12:124310228 | C | G | 2 | a0001c0003t0014g0069 a0001c0003t0014g0072 |
2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.208-1590C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310228 | |||||||
| chr12:124310244 | C | T | 1 | a0001c0002t0004g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.208-1574C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310244 | |||||||
| chr12:124310281 | A | G | 1 | a0001c0002t0002g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.208-1537A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310281 | |||||||
| chr12:124310300 | C | A | 1 | a0001c0001t0001g0316 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.208-1518C>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310300 | |||||||
| chr12:124310329 | G | A | 3 | a0001c0001t0001g0297 a0001c0001t0001g0332 a0001c0001t0012g0303 |
3 | NA18944.hp2 NA18948.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.208-1489G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310329 | |||||||
| chr12:124310492 | GGGGAGGG others(14): Show |
G | 352 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(349): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(357): Show |
intron_variant | MODIFIER | c.208-1302_208-1282d others(23): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310492 | ||||||
| chr12:124310493 | GGGAGGGG others(13): Show |
G | 1 | a0002c0005t0002g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.208-1322_208-1303d others(22): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310493 | ||||||
| chr12:124310510 | TGCAGGGA others(56): Show |
T | 5 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0047 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-1302_208-1240d others(65): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310510 | ||||||
| chr12:124310516 | G | A | 2 | a0001c0001t0004g0306 a0001c0001t0005g0258 |
2 | HG01169.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.208-1302G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310516 | |||||||
| chr12:124310517 | A | T | 2 | a0001c0001t0004g0306 a0001c0001t0005g0258 |
2 | HG01169.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.208-1301A>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310517 | |||||||
| chr12:124310522 | G | T | 2 | a0001c0001t0004g0306 a0001c0001t0005g0258 |
2 | HG01169.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.208-1296G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310522 | |||||||
| chr12:124310526 | T | G | 2 | a0001c0001t0004g0306 a0001c0001t0005g0258 |
2 | HG01169.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.208-1292T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310526 | |||||||
| chr12:124310528 | G | T | 2 | a0001c0001t0004g0306 a0001c0001t0005g0258 |
2 | HG01169.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.208-1290G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310528 | |||||||
| chr12:124310529 | A | C | 2 | a0001c0001t0004g0306 a0001c0001t0005g0258 |
2 | HG01169.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.208-1289A>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310529 | |||||||
| chr12:124310531 | T | TTAGGCCA others(14): Show |
2 | a0001c0001t0004g0306 a0001c0001t0005g0258 |
2 | HG01169.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.208-1287_208-1286i others(23): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310531 | |||||||
| chr12:124310544 | A | G | 2 | a0001c0001t0004g0306 a0001c0001t0005g0258 |
2 | HG01169.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.208-1274A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310544 | |||||||
| chr12:124310573 | A | G | 48 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(45): Show |
50 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.208-1245A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310573 | |||||||
| chr12:124310586 | G | A | 5 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0047 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-1232G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310586 | |||||||
| chr12:124310608 | G | GT | 5 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0047 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-1209dupT | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124310608 | ||||||
| chr12:124310737 | G | A | 1 | a0001c0001t0012g0357 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.208-1081G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124310737 | |||||||
| chr12:124311102 | C | T | 1 | a0001c0001t0011g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.208-716C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311102 | |||||||
| chr12:124311174 | G | A | 5 | a0001c0004t0002g0061 a0001c0004t0002g0270 a0003c0006t0018g0026 others(2): Show |
5 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-644G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311174 | |||||||
| chr12:124311270 | TCTGCTAT others(113): Show |
T | 70 | a0001c0001t0001g0314 a0001c0001t0002g0001 a0001c0001t0002g0014 others(67): Show |
73 | HG00140.hp1 HG00280.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.208-543_208-424del | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124311270 | ||||||
| chr12:124311274 | C | T | 1 | a0001c0003t0009g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208-544C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311274 | |||||||
| chr12:124311359 | C | T | 10 | a0001c0001t0005g0058 a0001c0001t0008g0110 a0001c0001t0008g0197 others(7): Show |
10 | HG01099.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.208-459C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311359 | |||||||
| chr12:124311461 | T | C | 257 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(254): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.208-357T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311461 | |||||||
| chr12:124311467 | G | C | 3 | a0003c0006t0018g0026 a0003c0006t0018g0033 a0003c0006t0018g0035 |
3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.208-351G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311467 | |||||||
| chr12:124311505 | G | A | 2 | a0001c0003t0014g0069 a0001c0003t0014g0072 |
2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.208-313G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311505 | |||||||
| chr12:124311548 | A | G | 2 | a0001c0001t0015g0278 a0001c0001t0015g0279 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.208-270A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311548 | |||||||
| chr12:124311564 | T | G | 145 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(142): Show |
148 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.208-254T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311564 | |||||||
| chr12:124311631 | C | T | 9 | a0001c0002t0002g0055 a0001c0002t0007g0372 a0001c0002t0017g0257 others(6): Show |
9 | HG01243.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-187C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311631 | |||||||
| chr12:124311651 | G | T | 1 | a0001c0001t0008g0217 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.208-167G>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311651 | |||||||
| chr12:124311651 | GGGCTTCC others(18): Show |
G | 1 | a0001c0002t0004g0263 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.208-146_208-122del others(25): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 124311651 | ||||||
| chr12:124311720 | G | C | 1 | a0001c0001t0001g0315 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.208-98G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311720 | |||||||
| chr12:124311756 | A | G | 1 | a0001c0002t0031g0371 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208-62A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 1/2 | chr12 | 124311756 | |||||||
| chr12:124311952 | C | T | 1 | a0001c0003t0014g0168 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.317+25C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124311952 | |||||||
| chr12:124311965 | T | C | 7 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(4): Show |
7 | HG00140.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.317+38T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124311965 | |||||||
| chr12:124312007 | G | A | 1 | a0004c0008t0035g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.317+80G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312007 | |||||||
| chr12:124312027 | G | A | 7 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(4): Show |
7 | HG00140.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.317+100G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312027 | |||||||
| chr12:124312173 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.317+246C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312173 | |||||||
| chr12:124312245 | T | G | 7 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(4): Show |
7 | HG00140.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.317+318T>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312245 | |||||||
| chr12:124312316 | A | AT | 137 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(134): Show |
141 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.317+403dupT | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 124312316 | ||||||
| chr12:124312316 | A | ATT | 27 | a0001c0002t0002g0049 a0001c0002t0002g0068 a0001c0002t0002g0073 others(24): Show |
28 | HG01070.hp1 HG01071.hp1 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.317+402_317+403dup others(2): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 124312316 | ||||||
| chr12:124312460 | G | A | 33 | a0001c0002t0007g0003 a0001c0002t0007g0012 a0001c0002t0007g0025 others(30): Show |
34 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.317+533G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312460 | |||||||
| chr12:124312519 | C | T | 1 | a0001c0002t0007g0372 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.317+592C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312519 | |||||||
| chr12:124312792 | TGCATATG others(2): Show |
T | 366 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(363): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.317+875_317+883del others(9): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 124312792 | ||||||
| chr12:124312912 | A | G | 10 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(7): Show |
10 | HG00140.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.317+985A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312912 | |||||||
| chr12:124312928 | G | A | 3 | a0003c0006t0018g0026 a0003c0006t0018g0033 a0003c0006t0018g0035 |
3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.317+1001G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312928 | |||||||
| chr12:124312943 | A | G | 7 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(4): Show |
7 | HG00140.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.317+1016A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312943 | |||||||
| chr12:124312957 | C | G | 10 | a0001c0001t0005g0058 a0001c0001t0008g0110 a0001c0001t0008g0197 others(7): Show |
10 | HG01099.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.317+1030C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312957 | |||||||
| chr12:124312963 | A | T | 10 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(7): Show |
10 | HG00140.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.317+1036A>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124312963 | |||||||
| chr12:124313195 | C | T | 10 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(7): Show |
10 | HG00140.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.318-997C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313195 | |||||||
| chr12:124313258 | T | C | 332 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(329): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.318-934T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313258 | |||||||
| chr12:124313336 | T | C | 1 | a0004c0008t0035g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.318-856T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313336 | |||||||
| chr12:124313396 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.318-796C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313396 | |||||||
| chr12:124313404 | C | T | 18 | a0001c0002t0007g0003 a0001c0002t0007g0078 a0001c0002t0007g0080 others(15): Show |
19 | HG01070.hp1 HG01071.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.318-788C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313404 | |||||||
| chr12:124313405 | G | A | 5 | a0001c0002t0017g0257 a0001c0002t0017g0260 a0001c0002t0017g0261 others(2): Show |
5 | HG01243.hp1 HG02647.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.318-787G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313405 | |||||||
| chr12:124313416 | T | C | 1 | a0001c0001t0001g0010 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.318-776T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313416 | |||||||
| chr12:124313445 | G | A | 1 | a0001c0002t0002g0027 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.318-747G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313445 | |||||||
| chr12:124313450 | G | A | 1 | a0001c0002t0003g0208 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.318-742G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313450 | |||||||
| chr12:124313453 | C | T | 10 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(7): Show |
10 | HG00140.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.318-739C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313453 | |||||||
| chr12:124313540 | A | G | 122 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(119): Show |
126 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.318-652A>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313540 | |||||||
| chr12:124313547 | C | T | 10 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(7): Show |
10 | HG00140.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.318-645C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313547 | |||||||
| chr12:124313565 | G | A | 1 | a0001c0002t0004g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.318-627G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313565 | |||||||
| chr12:124313678 | CA | C | 231 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(228): Show |
235 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.318-499delA | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 124313678 | ||||||
| chr12:124313819 | C | T | 3 | a0001c0001t0006g0141 a0001c0001t0006g0178 a0001c0001t0012g0363 |
3 | HG00642.hp1 HG01074.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.318-373C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313819 | |||||||
| chr12:124313867 | G | A | 150 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0038 others(147): Show |
152 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.318-325G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313867 | |||||||
| chr12:124313891 | C | T | 5 | a0001c0003t0014g0069 a0001c0003t0014g0072 a0001c0003t0014g0153 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.318-301C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313891 | |||||||
| chr12:124313915 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.318-277G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313915 | |||||||
| chr12:124313919 | C | G | 3 | a0003c0006t0018g0026 a0003c0006t0018g0033 a0003c0006t0018g0035 |
3 | HG01891.hp2 HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.318-273C>G | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313919 | |||||||
| chr12:124313919 | C | T | 1 | a0004c0008t0035g0169 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.318-273C>T | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313919 | |||||||
| chr12:124313972 | G | C | 10 | a0001c0001t0005g0058 a0001c0001t0008g0110 a0001c0001t0008g0197 others(7): Show |
10 | HG01099.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.318-220G>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313972 | |||||||
| chr12:124313980 | T | C | 2 | a0001c0002t0023g0192 a0001c0002t0023g0193 |
2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.318-212T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124313980 | |||||||
| chr12:124314036 | CCTT | C | 32 | a0001c0001t0006g0004 a0001c0001t0006g0109 a0001c0001t0006g0111 others(29): Show |
33 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.318-152_318-150del others(3): Show |
RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 124314036 | ||||||
| chr12:124314057 | T | C | 4 | a0001c0002t0002g0049 a0001c0002t0002g0068 a0001c0002t0002g0073 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-135T>C | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124314057 | |||||||
| chr12:124314117 | G | A | 7 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0037 others(4): Show |
7 | HG00140.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.318-75G>A | RFLNA | ENSG00000178882.15 | transcript | ENST00000546355.4 | protein_coding | 2/2 | chr12 | 124314117 |