Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8419 |
| ensemblid | ENSG00000170819.5 |
| hgncid | 1041 |
| symbol | BFSP2 |
| name | beaded filament structural protein 2 |
| refseq_nuc | NM_003571.4 |
| refseq_prot | NP_003562.1 |
| ensembl_nuc | ENST00000302334.3 |
| ensembl_prot | ENSP00000304987.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 133400056 |
| end | 133475208 |
| strand | + |
| ver | v1.2 |
| region | chr3:133400056-133475208 |
| region5000 | chr3:133395056-133480208 |
| regionname0 | BFSP2_chr3_133400056_133475208 |
| regionname5000 | BFSP2_chr3_133395056_133480208 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 414 | 263 | 80 | 52 | 90 | 8 | 31 | 65 | BFSP2_chr3_133395056_133480208 | BFSP2 | MSERR others(409): Show |
chr3 | 133395056 | 133480208 |
| a0002 | 0/0 | 414 | 9 | 1 | 2 | 2 | 2 | 2 | 2 | BFSP2_chr3_133395056_133480208 | BFSP2 | MSERR others(409): Show |
chr3 | 133395056 | 133480208 |
| a0003 | 0/0 | 414 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | MSERR others(409): Show |
chr3 | 133395056 | 133480208 |
| a0004 | 0/0 | 414 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | MSERR others(409): Show |
chr3 | 133395056 | 133480208 |
| a0005 | 0/0 | 414 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | MSERR others(409): Show |
chr3 | 133395056 | 133480208 |
| a0006 | 0/0 | 414 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | MSERR others(409): Show |
chr3 | 133395056 | 133480208 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1244 | 163 | 71 | 35 | 41 | 3 | 12 | BFSP2_chr3_133395056_133480208 | BFSP2 | ATGAG others(1239): Show |
chr3 | 133395056 | 133480208 | ||
| a0001c0002 | 0/1 | 1244 | 97 | 7 | 17 | 49 | 5 | 18 | BFSP2_chr3_133395056_133480208 | BFSP2 | ATGAG others(1239): Show |
chr3 | 133395056 | 133480208 | ||
| a0001c0004 | 0/0 | 1244 | 2 | 2 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | ATGAG others(1239): Show |
chr3 | 133395056 | 133480208 | ||
| a0001c0008 | 0/0 | 1244 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | ATGAG others(1239): Show |
chr3 | 133395056 | 133480208 | ||
| a0002c0003 | 0/0 | 1244 | 8 | 1 | 2 | 2 | 2 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | ATGAG others(1239): Show |
chr3 | 133395056 | 133480208 | ||
| a0002c0007 | 0/0 | 1244 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | ATGAG others(1239): Show |
chr3 | 133395056 | 133480208 | ||
| a0003c0010 | 0/0 | 1244 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | ATGAG others(1239): Show |
chr3 | 133395056 | 133480208 | ||
| a0004c0006 | 0/0 | 1244 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | ATGAG others(1239): Show |
chr3 | 133395056 | 133480208 | ||
| a0005c0005 | 0/0 | 1244 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | ATGAG others(1239): Show |
chr3 | 133395056 | 133480208 | ||
| a0006c0009 | 0/0 | 1244 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | ATGAG others(1239): Show |
chr3 | 133395056 | 133480208 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1511 | 163 | 71 | 35 | 41 | 3 | 12 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| a0001c0002t0001 | 0/1 | 1511 | 96 | 7 | 17 | 48 | 5 | 18 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| a0001c0002t0002 | 0/0 | 1511 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| a0001c0004t0001 | 0/0 | 1511 | 2 | 2 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| a0001c0008t0001 | 0/0 | 1511 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| a0002c0003t0001 | 0/0 | 1511 | 8 | 1 | 2 | 2 | 2 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| a0002c0007t0001 | 0/0 | 1511 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| a0003c0010t0001 | 0/0 | 1511 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| a0004c0006t0001 | 0/0 | 1511 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| a0005c0005t0001 | 0/0 | 1511 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| a0006c0009t0001 | 0/0 | 1511 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | ACTGG others(1506): Show |
chr3 | 133395056 | 133480208 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0004t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0001c0008t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0002c0007t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0003c0010t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0004c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0005c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| a0006c0009t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0227 | EUR | GBR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00558 | hp2 | a0003 | c0010 | t0001 | g0156 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | CHS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0262 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0257 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0178 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01515 | hp2 | a0002 | c0003 | t0001 | g0261 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0220 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0177 | EUR | IBS | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | CDX | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | CDX | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | KHV | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0145 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0131 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0219 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02738 | hp1 | a0002 | c0007 | t0001 | g0243 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0034 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0264 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0033 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03654 | hp1 | a0001 | c0008 | t0001 | g0125 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0211 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0263 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | PJL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0217 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0120 | SAS | BEB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0187 | SAS | STU | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | STU | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG04204 | hp2 | a0004 | c0006 | t0001 | g0172 | SAS | STU | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18952 | hp1 | a0005 | c0005 | t0001 | g0093 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0115 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18970 | hp1 | a0002 | c0003 | t0001 | g0119 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19030 | hp1 | a0006 | c0009 | t0001 | g0170 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0078 | EUR | TSI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0154 | EUR | TSI | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0083 | SAS | GIH | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | GIH | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | USA | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | USA | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | LWK | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0038 | REF | REF | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0167 | REF | REF | BFSP2_chr3_133395056_133480208 | BFSP2 | chr3 | 133395056 | 133480208 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:133400462 | C | G | 1 | a0003 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.379C>G | p.Gln127Glu | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/7 | 407/1512 | 379/1248 | 127/415 | chr3 | 133400462 | |||
| chr3:133400493 | G | A | 1 | a0005 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.410G>A | p.Arg137Gln | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/7 | 438/1512 | 410/1248 | 137/415 | chr3 | 133400493 | |||
| chr3:133400520 | G | A | 1 | a0004 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.437G>A | p.Arg146His | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/7 | 465/1512 | 437/1248 | 146/415 | chr3 | 133400520 | |||
| chr3:133447350 | A | G | 1 | a0006 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.523A>G | p.Met175Val | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/7 | 551/1512 | 523/1248 | 175/415 | chr3 | 133447350 | |||
| chr3:133472541 | C | A | 2 | a0002 a0004 |
10 | HG01069.hp2 HG01071.hp2 HG01515.hp2 others(7): Show |
missense_variant | MODERATE | c.1220C>A | p.Ala407Asp | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/7 | 1248/1512 | 1220/1248 | 407/415 | chr3 | 133472541 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:133400245 | C | T | 1 | a0001c0004 | 2 | HG03098.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.162C>T | p.Pro54Pro | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/7 | 190/1512 | 162/1248 | 54/415 | chr3 | 133400245 | |||
| chr3:133400452 | C | T | 1 | a0001c0004 | 2 | HG03098.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.369C>T | p.His123His | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/7 | 397/1512 | 369/1248 | 123/415 | chr3 | 133400452 | |||
| chr3:133448519 | G | A | 4 | a0001c0002 a0001c0008 a0002c0007 others(1): Show |
99 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
synonymous_variant | LOW | c.603G>A | p.Ala201Ala | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/7 | 631/1512 | 603/1248 | 201/415 | chr3 | 133448519 | |||
| chr3:133448636 | C | T | 1 | a0001c0008 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.720C>T | p.Asn240Asn | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/7 | 748/1512 | 720/1248 | 240/415 | chr3 | 133448636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:133475007 | C | T | 1 | a0001c0002t0002 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 7/7 | 35 | chr3 | 133475007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:133400782 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
136 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.489+210G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133400782 | |||||||
| chr3:133400858 | A | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0041 others(96): Show |
101 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.489+286A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133400858 | |||||||
| chr3:133400886 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(10): Show |
16 | HG01175.hp1 HG01255.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.489+314G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133400886 | |||||||
| chr3:133401437 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.489+865T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133401437 | |||||||
| chr3:133401512 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489+940T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133401512 | |||||||
| chr3:133402236 | A | G | 2 | a0001c0004t0001g0033 a0001c0004t0001g0034 |
2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.489+1664A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402236 | |||||||
| chr3:133402452 | A | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
7 | HG01175.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+1880A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402452 | |||||||
| chr3:133402497 | G | A | 1 | a0001c0002t0001g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.489+1925G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402497 | |||||||
| chr3:133402511 | TG | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | NA18522.hp2 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.489+1942delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133402511 | ||||||
| chr3:133402584 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.489+2012T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402584 | |||||||
| chr3:133402643 | C | CT | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(24): Show |
30 | HG01175.hp1 HG01255.hp2 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.489+2086dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133402643 | ||||||
| chr3:133402758 | A | G | 88 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0036 others(85): Show |
90 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.489+2186A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402758 | |||||||
| chr3:133402761 | G | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(25): Show |
31 | HG01175.hp1 HG01255.hp2 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.489+2189G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402761 | |||||||
| chr3:133402786 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.489+2214G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402786 | |||||||
| chr3:133402797 | C | T | 9 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+2225C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402797 | |||||||
| chr3:133402972 | C | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
7 | HG01175.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+2400C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133402972 | |||||||
| chr3:133403364 | C | A | 18 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(15): Show |
18 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+2792C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133403364 | |||||||
| chr3:133403364 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.489+2792C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133403364 | |||||||
| chr3:133403372 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(43): Show |
49 | HG00738.hp2 HG01175.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.489+2800A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133403372 | |||||||
| chr3:133403785 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(258): Show |
266 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.489+3213T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133403785 | |||||||
| chr3:133403961 | C | T | 2 | a0001c0002t0001g0131 a0001c0002t0001g0132 |
2 | HG02698.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.489+3389C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133403961 | |||||||
| chr3:133403998 | GA | G | 145 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(142): Show |
147 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.489+3428delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133403998 | ||||||
| chr3:133404086 | G | A | 2 | a0001c0004t0001g0033 a0001c0004t0001g0034 |
2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.489+3514G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404086 | |||||||
| chr3:133404113 | G | T | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0002t0001g0252 others(1): Show |
4 | NA18956.hp2 NA18969.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+3541G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404113 | |||||||
| chr3:133404419 | C | T | 1 | a0001c0002t0001g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.489+3847C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404419 | |||||||
| chr3:133404443 | A | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(36): Show |
42 | HG00738.hp2 HG01175.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.489+3871A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404443 | |||||||
| chr3:133404801 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.489+4229A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404801 | |||||||
| chr3:133404842 | C | A | 1 | a0001c0001t0001g0256 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.489+4270C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404842 | |||||||
| chr3:133404892 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
142 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.489+4320G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133404892 | |||||||
| chr3:133405113 | T | A | 2 | a0001c0002t0001g0016 a0001c0004t0001g0033 |
2 | HG03579.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.489+4541T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405113 | |||||||
| chr3:133405205 | C | T | 15 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0129 others(12): Show |
15 | HG01891.hp1 HG02056.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+4633C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405205 | |||||||
| chr3:133405519 | C | G | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02258.hp2 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+4947C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405519 | |||||||
| chr3:133405741 | G | A | 1 | a0001c0002t0001g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.489+5169G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405741 | |||||||
| chr3:133405755 | C | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(11): Show |
17 | HG01175.hp1 HG01255.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.489+5183C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405755 | |||||||
| chr3:133405812 | G | A | 1 | a0003c0010t0001g0156 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.489+5240G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405812 | |||||||
| chr3:133405878 | A | C | 1 | a0001c0004t0001g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.489+5306A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405878 | |||||||
| chr3:133405878 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(5): Show |
10 | HG01255.hp2 HG02109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+5306A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405878 | |||||||
| chr3:133405921 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(5): Show |
10 | HG01255.hp2 HG02109.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+5349C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405921 | |||||||
| chr3:133405982 | G | A | 1 | a0001c0004t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.489+5410G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133405982 | |||||||
| chr3:133406020 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0002t0001g0040 |
3 | HG01346.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.489+5448G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406020 | |||||||
| chr3:133406098 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.489+5526C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406098 | |||||||
| chr3:133406114 | C | CT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
11 | HG01255.hp2 HG02109.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.489+5543dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133406114 | ||||||
| chr3:133406116 | A | AT | 110 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(107): Show |
112 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.489+5558dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133406116 | ||||||
| chr3:133406116 | A | ATT | 10 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0112 others(7): Show |
10 | HG01081.hp2 HG02738.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+5557_489+5558d others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133406116 | ||||||
| chr3:133406116 | A | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
11 | HG01255.hp2 HG02109.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.489+5544A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406116 | |||||||
| chr3:133406141 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(12): Show |
18 | HG01175.hp1 HG01255.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.489+5569T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406141 | |||||||
| chr3:133406144 | A | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.489+5572A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406144 | |||||||
| chr3:133406327 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.489+5755G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406327 | |||||||
| chr3:133406371 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.489+5799C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406371 | |||||||
| chr3:133406560 | GCCATCTA others(4): Show |
G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
7 | HG01175.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+5991_489+6001d others(13): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133406560 | ||||||
| chr3:133406604 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.489+6032C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406604 | |||||||
| chr3:133406753 | G | A | 30 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
30 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.489+6181G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406753 | |||||||
| chr3:133406841 | A | G | 1 | a0001c0002t0001g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.489+6269A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406841 | |||||||
| chr3:133406869 | A | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(112): Show |
118 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.489+6297A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406869 | |||||||
| chr3:133406896 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.489+6324G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406896 | |||||||
| chr3:133406967 | G | A | 11 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0002t0001g0120 others(8): Show |
11 | HG02056.hp1 HG02129.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+6395G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133406967 | |||||||
| chr3:133407666 | C | T | 2 | a0001c0001t0001g0110 a0001c0002t0001g0111 |
2 | NA18969.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.489+7094C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133407666 | |||||||
| chr3:133407710 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.489+7138A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133407710 | |||||||
| chr3:133407809 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.489+7237C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133407809 | |||||||
| chr3:133407888 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.489+7316T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133407888 | |||||||
| chr3:133408092 | A | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
9 | HG01255.hp2 HG02109.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+7520A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408092 | |||||||
| chr3:133408113 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
7 | HG01175.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+7541T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408113 | |||||||
| chr3:133408138 | C | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0042 others(72): Show |
77 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.489+7566C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408138 | |||||||
| chr3:133408186 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
11 | HG01255.hp2 HG02109.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+7614A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408186 | |||||||
| chr3:133408190 | CTCTTTTA others(11): Show |
C | 1 | a0001c0002t0001g0159 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.489+7620_489+7637d others(20): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133408190 | ||||||
| chr3:133408611 | A | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG03239.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.489+8039A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408611 | |||||||
| chr3:133408668 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.489+8096G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408668 | |||||||
| chr3:133408821 | T | TG | 78 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0036 others(75): Show |
80 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.489+8250dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133408821 | ||||||
| chr3:133408908 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0149 |
3 | HG02615.hp1 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.489+8336G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133408908 | |||||||
| chr3:133409114 | A | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG01081.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+8542A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409114 | |||||||
| chr3:133409166 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.489+8594C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409166 | |||||||
| chr3:133409227 | G | GGT | 125 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0030 others(122): Show |
125 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.489+8684_489+8685d others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | ||||||
| chr3:133409227 | G | GGTGT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(9): Show |
13 | HG01175.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+8682_489+8685d others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | ||||||
| chr3:133409227 | G | GGTGTGT | 82 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0041 others(79): Show |
84 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.489+8680_489+8685d others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | ||||||
| chr3:133409227 | G | GGTGTGTG others(1): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
15 | HG01081.hp1 HG01081.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+8678_489+8685d others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | ||||||
| chr3:133409227 | G | GGTGTGTG others(3): Show |
6 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+8676_489+8685d others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | ||||||
| chr3:133409227 | G | GGTGTGTG others(5): Show |
1 | a0001c0004t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.489+8674_489+8685d others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | ||||||
| chr3:133409227 | G | GGTGTGTG others(7): Show |
9 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+8672_489+8685d others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133409227 | ||||||
| chr3:133409286 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.489+8714T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409286 | |||||||
| chr3:133409380 | T | A | 105 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(102): Show |
107 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.489+8808T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409380 | |||||||
| chr3:133409605 | T | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
134 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.489+9033T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409605 | |||||||
| chr3:133409634 | C | A | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.489+9062C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409634 | |||||||
| chr3:133409704 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.489+9132C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133409704 | |||||||
| chr3:133410099 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.489+9527T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133410099 | |||||||
| chr3:133410260 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.489+9688C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133410260 | |||||||
| chr3:133410310 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.489+9738T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133410310 | |||||||
| chr3:133410428 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(89): Show |
94 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.489+9856C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133410428 | |||||||
| chr3:133410491 | C | T | 1 | a0002c0007t0001g0243 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.489+9919C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133410491 | |||||||
| chr3:133411061 | C | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
83 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.489+10489C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411061 | |||||||
| chr3:133411108 | T | G | 77 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0042 others(74): Show |
79 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.489+10536T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411108 | |||||||
| chr3:133411154 | T | A | 1 | a0001c0001t0001g0259 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.489+10582T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411154 | |||||||
| chr3:133411179 | C | T | 2 | a0001c0001t0001g0030 a0001c0002t0001g0031 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.489+10607C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411179 | |||||||
| chr3:133411180 | GA | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0022 others(38): Show |
41 | HG00738.hp2 HG01123.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.489+10627delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133411180 | ||||||
| chr3:133411180 | GAA | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(130): Show |
134 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.489+10626_489+1062 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133411180 | ||||||
| chr3:133411180 | GAAA | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(22): Show |
27 | HG00099.hp2 HG00438.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.489+10625_489+1062 others(7): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133411180 | ||||||
| chr3:133411180 | GAAAA | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0023 others(61): Show |
66 | HG00438.hp2 HG01069.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.489+10624_489+1062 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133411180 | ||||||
| chr3:133411199 | A | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0265 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.489+10627A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411199 | |||||||
| chr3:133411573 | A | C | 1 | a0001c0002t0001g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.489+11001A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411573 | |||||||
| chr3:133411625 | A | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0041 others(32): Show |
37 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.489+11053A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411625 | |||||||
| chr3:133411721 | CA | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
256 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(253): Show |
intron_variant | MODIFIER | c.489+11151delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133411721 | ||||||
| chr3:133411729 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(126): Show |
132 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.489+11157C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411729 | |||||||
| chr3:133411934 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.489+11362T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133411934 | |||||||
| chr3:133412004 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.489+11432G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412004 | |||||||
| chr3:133412005 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.489+11433A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412005 | |||||||
| chr3:133412026 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.489+11454C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412026 | |||||||
| chr3:133412035 | C | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(230): Show |
237 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.489+11463C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412035 | |||||||
| chr3:133412044 | G | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0015 others(7): Show |
10 | HG02257.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+11472G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412044 | |||||||
| chr3:133412080 | C | A | 7 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0149 others(4): Show |
7 | HG01258.hp1 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+11508C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412080 | |||||||
| chr3:133412161 | C | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+11589C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412161 | |||||||
| chr3:133412456 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.489+11884C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412456 | |||||||
| chr3:133412572 | T | C | 2 | a0001c0002t0001g0124 a0001c0008t0001g0125 |
2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.489+12000T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412572 | |||||||
| chr3:133412618 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.489+12046G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412618 | |||||||
| chr3:133412784 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.489+12212G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412784 | |||||||
| chr3:133412872 | G | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0250 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+12300G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133412872 | |||||||
| chr3:133413037 | C | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0149 |
3 | HG02922.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.489+12465C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413037 | |||||||
| chr3:133413055 | T | C | 10 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0100 others(7): Show |
10 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+12483T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413055 | |||||||
| chr3:133413149 | T | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0250 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+12577T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413149 | |||||||
| chr3:133413182 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0250 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+12610G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413182 | |||||||
| chr3:133413208 | C | T | 10 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0100 others(7): Show |
10 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+12636C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413208 | |||||||
| chr3:133413335 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.489+12763C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413335 | |||||||
| chr3:133413353 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.489+12781C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413353 | |||||||
| chr3:133413652 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.489+13080G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413652 | |||||||
| chr3:133413845 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489+13273T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413845 | |||||||
| chr3:133413846 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489+13274A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413846 | |||||||
| chr3:133413953 | C | T | 1 | a0001c0002t0001g0128 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.489+13381C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133413953 | |||||||
| chr3:133414035 | CCT | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0024 others(9): Show |
12 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+13469_489+1347 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414035 | ||||||
| chr3:133414243 | CCT | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0024 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+13672_489+1367 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133414243 | |||||||
| chr3:133414251 | G | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.489+13679G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133414251 | |||||||
| chr3:133414269 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.489+13697G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133414269 | |||||||
| chr3:133414281 | TACTC | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0032 others(19): Show |
22 | HG01123.hp2 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.489+13712_489+1371 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414281 | ||||||
| chr3:133414717 | A | ATCCCCTC others(42): Show |
1 | a0001c0001t0001g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489+14166_489+1416 others(53): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414717 | ||||||
| chr3:133414717 | A | ATCCCCTC others(41): Show |
9 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0100 others(6): Show |
9 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+14166_489+1416 others(52): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414717 | ||||||
| chr3:133414717 | A | ATCCCCTC others(41): Show |
20 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(17): Show |
20 | HG00639.hp1 HG02109.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.489+14166_489+1416 others(52): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414717 | ||||||
| chr3:133414717 | A | ATCCCCTC others(65): Show |
214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(211): Show |
219 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.489+14166_489+1416 others(76): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414717 | ||||||
| chr3:133414717 | A | ATCTCCTC others(41): Show |
24 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0018 others(21): Show |
24 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.489+14147_489+1414 others(52): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414717 | ||||||
| chr3:133414786 | AC | A | 43 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0018 others(40): Show |
43 | HG00621.hp2 HG00639.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.489+14224delC | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414786 | ||||||
| chr3:133414786 | ACC | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
199 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.489+14223_489+1422 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414786 | ||||||
| chr3:133414792 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.489+14220C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133414792 | |||||||
| chr3:133414853 | A | C | 10 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0100 others(7): Show |
10 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+14281A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133414853 | |||||||
| chr3:133414863 | ACCTGCCC others(17): Show |
A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.489+14296_489+1431 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414863 | ||||||
| chr3:133414958 | CCCTCTAC others(17): Show |
C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG01243.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.489+14400_489+1442 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133414958 | ||||||
| chr3:133415061 | C | T | 10 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0100 others(7): Show |
10 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+14489C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415061 | |||||||
| chr3:133415068 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.489+14496C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415068 | |||||||
| chr3:133415220 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.489+14648C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415220 | |||||||
| chr3:133415222 | CCTCACCT others(467): Show |
C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0024 others(9): Show |
12 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+14657_489+1513 others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133415222 | ||||||
| chr3:133415229 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(225): Show |
233 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.489+14657T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415229 | |||||||
| chr3:133415274 | A | ACCCTTGC others(5): Show |
1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14705_489+1470 others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133415274 | ||||||
| chr3:133415286 | A | G | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14714A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415286 | |||||||
| chr3:133415290 | T | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(10): Show |
13 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+14718T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415290 | |||||||
| chr3:133415293 | C | T | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14721C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415293 | |||||||
| chr3:133415297 | C | T | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14725C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415297 | |||||||
| chr3:133415310 | G | A | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14738G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415310 | |||||||
| chr3:133415314 | C | G | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14742C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415314 | |||||||
| chr3:133415321 | T | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(13): Show |
16 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(13): Show |
intron_variant | MODIFIER | c.489+14749T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415321 | |||||||
| chr3:133415338 | G | C | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14766G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415338 | |||||||
| chr3:133415341 | T | C | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+14769T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415341 | |||||||
| chr3:133415348 | C | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
74 | HG00099.hp2 HG00621.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.489+14776C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415348 | |||||||
| chr3:133415351 | T | C | 72 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
74 | HG00099.hp2 HG00621.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.489+14779T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415351 | |||||||
| chr3:133415351 | T | TCTACTCA others(17): Show |
184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(181): Show |
187 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.489+14791_489+1479 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133415351 | ||||||
| chr3:133415482 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.489+14910C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415482 | |||||||
| chr3:133415549 | CCTCTACT others(17): Show |
C | 20 | a0001c0001t0001g0056 a0001c0001t0001g0070 a0001c0001t0001g0079 others(17): Show |
20 | HG00621.hp2 HG00738.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.489+15016_489+1503 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133415549 | ||||||
| chr3:133415572 | C | T | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+15000C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415572 | |||||||
| chr3:133415596 | C | T | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+15024C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415596 | |||||||
| chr3:133415617 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.489+15045C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415617 | |||||||
| chr3:133415676 | TCCCCTCT others(5): Show |
T | 21 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0070 others(18): Show |
21 | HG00621.hp2 HG00738.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.489+15122_489+1513 others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133415676 | ||||||
| chr3:133415703 | CCT | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0149 |
3 | HG02922.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.489+15132_489+1513 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415703 | |||||||
| chr3:133415967 | G | T | 1 | a0001c0002t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.489+15395G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415967 | |||||||
| chr3:133415987 | CT | C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0001g0265 |
3 | HG02451.hp1 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.489+15416delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133415987 | |||||||
| chr3:133416012 | G | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0149 |
3 | HG02922.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.489+15440G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416012 | |||||||
| chr3:133416033 | CCT | C | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+15462_489+1546 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416033 | |||||||
| chr3:133416119 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.489+15547T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416119 | |||||||
| chr3:133416161 | CCTCTCCC others(17): Show |
C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.489+15599_489+1562 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133416161 | ||||||
| chr3:133416249 | TCCCCTGT others(17): Show |
T | 2 | a0001c0001t0001g0026 a0002c0003t0001g0145 |
2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.489+15690_489+1571 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133416249 | ||||||
| chr3:133416295 | T | C | 1 | a0002c0003t0001g0219 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.489+15723T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416295 | |||||||
| chr3:133416312 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(149): Show |
155 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.489+15740C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416312 | |||||||
| chr3:133416325 | G | A | 1 | a0001c0002t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.489+15753G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416325 | |||||||
| chr3:133416363 | A | G | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+15791A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416363 | |||||||
| chr3:133416398 | C | A | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0002t0001g0080 |
3 | HG00438.hp2 NA19084.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.489+15826C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416398 | |||||||
| chr3:133416405 | C | T | 2 | a0001c0001t0001g0251 a0001c0002t0001g0169 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+15833C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416405 | |||||||
| chr3:133416436 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(265): Show |
273 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.489+15864G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416436 | |||||||
| chr3:133416459 | T | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(22): Show |
25 | HG01099.hp2 HG02109.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.489+15887T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416459 | |||||||
| chr3:133416516 | C | T | 1 | a0001c0002t0001g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.489+15944C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416516 | |||||||
| chr3:133416574 | AC | A | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+16006delC | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133416574 | ||||||
| chr3:133416580 | TCCATCTC others(17): Show |
T | 1 | a0001c0002t0001g0121 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.489+16020_489+1604 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133416580 | ||||||
| chr3:133416633 | C | T | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+16061C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416633 | |||||||
| chr3:133416766 | C | T | 19 | a0001c0001t0001g0056 a0001c0001t0001g0070 a0001c0001t0001g0079 others(16): Show |
19 | HG00621.hp2 HG00738.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.489+16194C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416766 | |||||||
| chr3:133416821 | C | CCTCTCCC others(17): Show |
24 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0018 others(21): Show |
24 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.489+16256_489+1625 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133416821 | ||||||
| chr3:133416979 | C | T | 5 | a0001c0002t0001g0077 a0001c0002t0001g0090 a0001c0002t0001g0213 others(2): Show |
5 | NA18947.hp2 NA18952.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+16407C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133416979 | |||||||
| chr3:133417035 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0127 a0001c0001t0001g0209 |
3 | NA18946.hp1 NA18947.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.489+16463C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417035 | |||||||
| chr3:133417092 | C | CTCTCCCC others(17): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0222 a0001c0002t0001g0045 |
3 | NA18993.hp1 NA18999.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.489+16534_489+1655 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417092 | ||||||
| chr3:133417132 | C | T | 1 | a0001c0002t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.489+16560C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417132 | |||||||
| chr3:133417138 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0149 |
3 | HG02922.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.489+16566C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417138 | |||||||
| chr3:133417165 | C | G | 1 | a0001c0002t0001g0128 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.489+16593C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417165 | |||||||
| chr3:133417176 | T | G | 2 | a0001c0001t0001g0251 a0001c0002t0001g0169 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+16604T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417176 | |||||||
| chr3:133417206 | CGCCTCTC others(17): Show |
C | 2 | a0001c0001t0001g0251 a0001c0002t0001g0169 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+16635_489+1665 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417206 | |||||||
| chr3:133417231 | T | A | 2 | a0001c0001t0001g0251 a0001c0002t0001g0169 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+16659T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417231 | |||||||
| chr3:133417279 | CCCTCTCC others(17): Show |
C | 1 | a0001c0001t0001g0209 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.489+16712_489+1673 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417279 | ||||||
| chr3:133417285 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0149 |
3 | HG02922.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.489+16713C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417285 | |||||||
| chr3:133417309 | C | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0137 others(1): Show |
4 | HG02257.hp1 HG02615.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+16737C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417309 | |||||||
| chr3:133417309 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.489+16737C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417309 | |||||||
| chr3:133417373 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.489+16801C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417373 | |||||||
| chr3:133417443 | A | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0127 a0001c0001t0001g0209 |
3 | NA18946.hp1 NA18947.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.489+16871A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417443 | |||||||
| chr3:133417524 | C | CCCA | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
129 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.489+16953_489+1695 others(7): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417524 | ||||||
| chr3:133417592 | CCCTCTAC others(5): Show |
C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(12): Show |
15 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.489+17036_489+1704 others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417592 | ||||||
| chr3:133417594 | C | CTCTACTC others(24): Show |
1 | a0001c0002t0001g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.489+17025_489+1705 others(35): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417594 | ||||||
| chr3:133417674 | T | C | 1 | a0001c0002t0001g0091 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.489+17102T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417674 | |||||||
| chr3:133417677 | T | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0025 others(17): Show |
22 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.489+17105T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417677 | |||||||
| chr3:133417747 | C | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0018 others(21): Show |
24 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.489+17175C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417747 | |||||||
| chr3:133417831 | T | C | 1 | a0001c0002t0001g0111 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.489+17259T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417831 | |||||||
| chr3:133417839 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.489+17267C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417839 | |||||||
| chr3:133417843 | C | T | 2 | a0001c0001t0001g0134 a0001c0002t0001g0111 |
2 | NA18970.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.489+17271C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417843 | |||||||
| chr3:133417843 | CGTCCTCT others(17): Show |
C | 2 | a0001c0002t0001g0150 a0001c0002t0001g0151 |
2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.489+17317_489+1734 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133417843 | ||||||
| chr3:133417858 | AC | A | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+17287delC | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133417858 | |||||||
| chr3:133418007 | ATTCTACT others(101): Show |
A | 2 | a0001c0001t0001g0251 a0001c0002t0001g0169 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+17469_489+1757 others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133418007 | ||||||
| chr3:133418022 | GTCCTCTC others(17): Show |
G | 20 | a0001c0001t0001g0056 a0001c0001t0001g0070 a0001c0001t0001g0079 others(17): Show |
20 | HG00621.hp2 HG00738.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.489+17469_489+1749 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133418022 | ||||||
| chr3:133418032 | CTCTACTC others(77): Show |
C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG02109.hp1 HG02717.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.489+17469_489+1755 others(88): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133418032 | ||||||
| chr3:133418046 | ATCCTCTC others(77): Show |
A | 1 | a0001c0001t0001g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.489+17498_489+1758 others(88): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133418046 | ||||||
| chr3:133418089 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0071 others(8): Show |
11 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.489+17517C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418089 | |||||||
| chr3:133418095 | A | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(28): Show |
33 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.489+17523A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418095 | |||||||
| chr3:133418244 | T | C | 39 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(36): Show |
39 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.489+17672T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418244 | |||||||
| chr3:133418355 | C | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(34): Show |
37 | HG00639.hp1 HG00639.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.489+17783C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418355 | |||||||
| chr3:133418440 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(171): Show |
177 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.489+17868G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418440 | |||||||
| chr3:133418579 | T | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0056 others(28): Show |
31 | HG00621.hp2 HG00738.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.489+18007T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418579 | |||||||
| chr3:133418590 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(167): Show |
174 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.489+18018G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418590 | |||||||
| chr3:133418710 | C | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0072 others(9): Show |
13 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+18138C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418710 | |||||||
| chr3:133418820 | A | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.489+18248A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418820 | |||||||
| chr3:133418843 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.489+18271G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418843 | |||||||
| chr3:133418982 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.489+18410C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133418982 | |||||||
| chr3:133419132 | A | ATCTGTGT others(4699): Show |
1 | a0001c0002t0001g0252 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.489+18695_489+1869 others(4710): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133419132 | ||||||
| chr3:133419146 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.489+18574T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419146 | |||||||
| chr3:133419192 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(105): Show |
111 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.489+18620G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419192 | |||||||
| chr3:133419268 | C | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.489+18696C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419268 | |||||||
| chr3:133419318 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.489+18746C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419318 | |||||||
| chr3:133419351 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.489+18779G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419351 | |||||||
| chr3:133419459 | C | A | 2 | a0001c0001t0001g0112 a0001c0004t0001g0033 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.489+18887C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419459 | |||||||
| chr3:133419495 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.489+18923T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419495 | |||||||
| chr3:133419636 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0148 a0001c0001t0001g0265 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+19064C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419636 | |||||||
| chr3:133419834 | A | G | 1 | a0001c0002t0001g0128 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.489+19262A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419834 | |||||||
| chr3:133419922 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0056 others(26): Show |
29 | HG00621.hp2 HG00738.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.489+19350C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419922 | |||||||
| chr3:133419944 | C | T | 2 | a0001c0002t0001g0131 a0001c0002t0001g0211 |
2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.489+19372C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133419944 | |||||||
| chr3:133420134 | G | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.489+19562G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420134 | |||||||
| chr3:133420166 | T | C | 10 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0100 others(7): Show |
10 | HG01099.hp2 HG02165.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+19594T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420166 | |||||||
| chr3:133420409 | G | T | 2 | a0001c0002t0001g0088 a0001c0002t0001g0089 |
2 | HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.489+19837G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420409 | |||||||
| chr3:133420553 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.489+19981A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420553 | |||||||
| chr3:133420601 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.489+20029C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420601 | |||||||
| chr3:133420628 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.489+20056A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420628 | |||||||
| chr3:133420730 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0265 |
2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.489+20158C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420730 | |||||||
| chr3:133420941 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.489+20369C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133420941 | |||||||
| chr3:133421002 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
173 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.489+20430C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421002 | |||||||
| chr3:133421046 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.489+20474G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421046 | |||||||
| chr3:133421148 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.489+20576G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421148 | |||||||
| chr3:133421175 | T | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(4): Show |
10 | HG01255.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+20603T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421175 | |||||||
| chr3:133421264 | G | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0072 others(10): Show |
14 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+20692G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421264 | |||||||
| chr3:133421348 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0188 a0001c0001t0001g0214 |
3 | NA18962.hp1 NA18990.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.489+20776A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421348 | |||||||
| chr3:133421353 | C | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0072 others(10): Show |
14 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+20781C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421353 | |||||||
| chr3:133421354 | A | G | 1 | a0001c0002t0001g0262 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.489+20782A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421354 | |||||||
| chr3:133421374 | G | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
264 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.489+20802G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421374 | |||||||
| chr3:133421383 | C | G | 1 | a0001c0002t0001g0255 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.489+20811C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421383 | |||||||
| chr3:133421383 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.489+20811C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421383 | |||||||
| chr3:133421410 | G | A | 2 | a0001c0001t0001g0251 a0001c0002t0001g0169 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.489+20838G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421410 | |||||||
| chr3:133421417 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.489+20845C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421417 | |||||||
| chr3:133421426 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.489+20854C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421426 | |||||||
| chr3:133421479 | C | T | 16 | a0001c0001t0001g0056 a0001c0001t0001g0070 a0001c0001t0001g0079 others(13): Show |
16 | HG00621.hp2 HG00738.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.489+20907C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421479 | |||||||
| chr3:133421481 | A | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0072 others(10): Show |
14 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+20909A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421481 | |||||||
| chr3:133421497 | A | ACTTCCTC others(2347): Show |
1 | a0001c0002t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.489+20925_489+2092 others(2358): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421497 | |||||||
| chr3:133421501 | T | C | 1 | a0001c0002t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.489+20929T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421501 | |||||||
| chr3:133421658 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(173): Show |
180 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.489+21086G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421658 | |||||||
| chr3:133421834 | C | T | 1 | a0001c0002t0001g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.489+21262C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421834 | |||||||
| chr3:133421886 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.489+21314A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421886 | |||||||
| chr3:133421920 | T | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
37 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.489+21348T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133421920 | |||||||
| chr3:133422000 | G | A | 10 | a0001c0001t0001g0032 a0001c0001t0001g0158 a0001c0001t0001g0162 others(7): Show |
10 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+21428G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422000 | |||||||
| chr3:133422063 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.489+21491C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422063 | |||||||
| chr3:133422076 | C | CAGCCTGG others(6): Show |
1 | a0001c0001t0001g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.489+21508_489+2152 others(17): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422076 | ||||||
| chr3:133422105 | C | CA | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(139): Show |
145 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.489+21554dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422105 | ||||||
| chr3:133422105 | C | CAA | 37 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0044 others(34): Show |
37 | HG00423.hp2 HG00738.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.489+21553_489+2155 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422105 | ||||||
| chr3:133422105 | C | CAAA | 22 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
23 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.489+21552_489+2155 others(7): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422105 | ||||||
| chr3:133422105 | C | CAAAA | 11 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0001g0141 others(8): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+21551_489+2155 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422105 | ||||||
| chr3:133422105 | C | CAAAAA | 23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
23 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.489+21550_489+2155 others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422105 | ||||||
| chr3:133422164 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.489+21592T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422164 | |||||||
| chr3:133422375 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.489+21803G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422375 | |||||||
| chr3:133422476 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0212 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.489+21904C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422476 | |||||||
| chr3:133422765 | C | CTGCCAGA others(15): Show |
221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
226 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.489+22199_489+2222 others(26): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422765 | ||||||
| chr3:133422765 | C | CTGCCAGA others(14): Show |
1 | a0001c0001t0001g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.489+22209_489+2221 others(25): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422765 | ||||||
| chr3:133422784 | G | GTGTTGCC others(15): Show |
1 | a0001c0001t0001g0212 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.489+22220_489+2222 others(26): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422784 | ||||||
| chr3:133422791 | C | CAGAATAT others(16): Show |
1 | a0001c0002t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.489+22220_489+2222 others(27): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133422791 | ||||||
| chr3:133422796 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.489+22224A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422796 | |||||||
| chr3:133422803 | T | G | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.489+22231T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422803 | |||||||
| chr3:133422830 | T | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0026 others(13): Show |
17 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.489+22258T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422830 | |||||||
| chr3:133422853 | C | T | 11 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0110 others(8): Show |
11 | HG02055.hp1 HG02165.hp1 HG03471.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+22281C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133422853 | |||||||
| chr3:133423270 | G | A | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.489+22698G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423270 | |||||||
| chr3:133423316 | T | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(36): Show |
40 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.489+22744T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423316 | |||||||
| chr3:133423458 | T | G | 1 | a0001c0001t0001g0044 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.489+22886T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423458 | |||||||
| chr3:133423478 | G | A | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(49): Show |
52 | HG00735.hp2 HG01106.hp2 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.489+22906G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423478 | |||||||
| chr3:133423540 | G | T | 1 | a0001c0002t0001g0208 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.489+22968G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423540 | |||||||
| chr3:133423610 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.489+23038A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423610 | |||||||
| chr3:133423706 | G | T | 1 | a0001c0002t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.489+23134G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423706 | |||||||
| chr3:133423748 | T | G | 1 | a0001c0002t0001g0208 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.489+23176T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423748 | |||||||
| chr3:133423749 | G | T | 1 | a0001c0002t0001g0208 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.489+23177G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423749 | |||||||
| chr3:133423767 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.489+23195C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423767 | |||||||
| chr3:133423903 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0022 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+23331C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423903 | |||||||
| chr3:133423916 | C | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.489+23344C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133423916 | |||||||
| chr3:133424009 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.490-23308G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424009 | |||||||
| chr3:133424039 | C | CT | 59 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(56): Show |
60 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.490-23267dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424039 | ||||||
| chr3:133424212 | ATTTTTTT others(5): Show |
A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(45): Show |
49 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.490-23087_490-2307 others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424212 | ||||||
| chr3:133424214 | T | TTGTGTGT others(17): Show |
1 | a0001c0001t0001g0004 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.490-23102_490-2310 others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424214 | ||||||
| chr3:133424214 | T | TTGTGTGT others(19): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0266 |
2 | HG01081.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.490-23102_490-2310 others(30): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424214 | ||||||
| chr3:133424214 | T | TTGTGTGT others(31): Show |
1 | a0001c0001t0001g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.490-23102_490-2310 others(42): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424214 | ||||||
| chr3:133424216 | T | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0140 others(2): Show |
6 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-23101T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424216 | |||||||
| chr3:133424216 | T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.490-23101_490-2310 others(23): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424216 | |||||||
| chr3:133424216 | T | TTG | 16 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0061 others(13): Show |
16 | HG02055.hp1 HG02165.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.490-23100_490-2309 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | ||||||
| chr3:133424216 | T | TTGTG | 10 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0134 others(7): Show |
10 | HG01099.hp1 HG01167.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-23100_490-2309 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | ||||||
| chr3:133424216 | T | TTGTGTG | 5 | a0001c0001t0001g0070 a0001c0001t0001g0157 a0001c0002t0001g0063 others(2): Show |
5 | HG00738.hp1 HG01069.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-23100_490-2309 others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | ||||||
| chr3:133424216 | T | TTGTGTGT others(9): Show |
8 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0024 others(5): Show |
8 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-23100_490-2309 others(20): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | ||||||
| chr3:133424216 | T | TTGTGTGT others(13): Show |
1 | a0001c0001t0001g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-23100_490-2309 others(24): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | ||||||
| chr3:133424216 | T | TTGTGTGT others(21): Show |
1 | a0001c0001t0001g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.490-23100_490-2309 others(32): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | ||||||
| chr3:133424216 | T | TTGTGTGT others(29): Show |
1 | a0001c0001t0001g0141 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.490-23100_490-2309 others(40): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | ||||||
| chr3:133424216 | T | TTGTGTGT others(31): Show |
1 | a0001c0001t0001g0142 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.490-23100_490-2309 others(42): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | ||||||
| chr3:133424216 | T | TTGTGTGT others(33): Show |
1 | a0001c0002t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-23100_490-2309 others(44): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424216 | ||||||
| chr3:133424218 | T | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(47): Show |
51 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.490-23099T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424218 | |||||||
| chr3:133424218 | T | TTGTG | 17 | a0001c0001t0001g0108 a0001c0001t0001g0155 a0001c0001t0001g0242 others(14): Show |
17 | HG00438.hp1 HG00438.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.490-23098_490-2309 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424218 | ||||||
| chr3:133424220 | T | G | 68 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(65): Show |
69 | HG00438.hp1 HG00438.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.490-23097T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424220 | |||||||
| chr3:133424220 | T | TTGTG | 43 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(40): Show |
45 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.490-23096_490-2309 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424220 | ||||||
| chr3:133424220 | T | TTGTGTG | 11 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0210 others(8): Show |
11 | HG00639.hp1 HG01516.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-23096_490-2309 others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424220 | ||||||
| chr3:133424222 | T | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(121): Show |
127 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.490-23095T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424222 | |||||||
| chr3:133424222 | T | TGTGTG | 3 | a0001c0001t0001g0228 a0001c0002t0001g0120 a0001c0002t0001g0223 |
3 | HG04184.hp2 NA18964.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.490-23095_490-2309 others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424222 | |||||||
| chr3:133424222 | T | TTGTG | 49 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0043 others(46): Show |
50 | HG00558.hp1 HG00558.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.490-23094_490-2309 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424222 | ||||||
| chr3:133424222 | T | TTGTGTG | 10 | a0001c0001t0001g0052 a0001c0001t0001g0205 a0001c0001t0001g0209 others(7): Show |
10 | NA18946.hp1 NA18946.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-23094_490-2309 others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424222 | ||||||
| chr3:133424222 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-23094_490-2309 others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424222 | ||||||
| chr3:133424224 | T | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(188): Show |
195 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.490-23093T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424224 | |||||||
| chr3:133424226 | T | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
198 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.490-23091T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424226 | |||||||
| chr3:133424228 | T | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(193): Show |
200 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.490-23089T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424228 | |||||||
| chr3:133424230 | T | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(193): Show |
200 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.490-23087T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424230 | |||||||
| chr3:133424232 | T | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(206): Show |
213 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.490-23085T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424232 | |||||||
| chr3:133424234 | T | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-23083T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424234 | |||||||
| chr3:133424236 | T | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-23081T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424236 | |||||||
| chr3:133424238 | T | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-23079T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424238 | |||||||
| chr3:133424240 | T | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-23077T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424240 | |||||||
| chr3:133424244 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.490-23073A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424244 | |||||||
| chr3:133424244 | A | T | 1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-23073A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424244 | |||||||
| chr3:133424413 | C | CTTTTTCA others(38): Show |
1 | a0001c0001t0001g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.490-22902_490-2285 others(49): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424413 | ||||||
| chr3:133424474 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-22843A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424474 | |||||||
| chr3:133424511 | TG | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-22805delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424511 | |||||||
| chr3:133424548 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-22769T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424548 | |||||||
| chr3:133424583 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-22734T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424583 | |||||||
| chr3:133424605 | GGTTT | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0147 a0001c0002t0001g0206 |
3 | HG00423.hp1 HG00423.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.490-22703_490-2270 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133424605 | ||||||
| chr3:133424625 | T | G | 1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.490-22692T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424625 | |||||||
| chr3:133424661 | A | C | 1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.490-22656A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424661 | |||||||
| chr3:133424668 | C | T | 1 | a0001c0002t0001g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.490-22649C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424668 | |||||||
| chr3:133424669 | T | G | 10 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0163 others(7): Show |
10 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-22648T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424669 | |||||||
| chr3:133424786 | A | C | 1 | a0001c0001t0001g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-22531A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424786 | |||||||
| chr3:133424812 | T | G | 1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.490-22505T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424812 | |||||||
| chr3:133424880 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.490-22437T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133424880 | |||||||
| chr3:133425026 | T | TG | 3 | a0001c0001t0001g0148 a0001c0002t0001g0131 a0001c0002t0001g0215 |
3 | HG02622.hp2 HG02698.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.490-22288dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425026 | ||||||
| chr3:133425177 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0158 |
2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-22140T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425177 | |||||||
| chr3:133425195 | A | C | 1 | a0001c0002t0001g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490-22122A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425195 | |||||||
| chr3:133425224 | A | G | 1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-22093A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425224 | |||||||
| chr3:133425225 | G | GGGGGGGG others(9): Show |
1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-22092_490-2209 others(20): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425225 | |||||||
| chr3:133425235 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-22082T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425235 | |||||||
| chr3:133425423 | C | T | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(45): Show |
49 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.490-21894C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425423 | |||||||
| chr3:133425433 | G | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0138 a0002c0003t0001g0145 |
3 | HG02280.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.490-21884G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425433 | |||||||
| chr3:133425451 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490-21866C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425451 | |||||||
| chr3:133425527 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-21790G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425527 | |||||||
| chr3:133425539 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(239): Show |
247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.490-21778A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425539 | |||||||
| chr3:133425611 | A | G | 1 | a0001c0002t0001g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.490-21706A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425611 | |||||||
| chr3:133425644 | G | A | 1 | a0001c0002t0001g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.490-21673G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425644 | |||||||
| chr3:133425762 | G | GACGGGAA others(5): Show |
1 | a0006c0009t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-21554_490-2155 others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425762 | ||||||
| chr3:133425762 | GATGGGA | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0024 others(13): Show |
16 | HG00738.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.490-21553_490-2154 others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425762 | ||||||
| chr3:133425764 | T | A | 2 | a0001c0001t0001g0148 a0006c0009t0001g0170 |
2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.490-21553T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425764 | |||||||
| chr3:133425764 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(223): Show |
231 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.490-21553T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425764 | |||||||
| chr3:133425768 | AAAGGGAA others(4): Show |
A | 1 | a0001c0001t0001g0265 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.490-21546_490-2153 others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425768 | ||||||
| chr3:133425770 | A | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0024 others(13): Show |
16 | HG00738.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.490-21547A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425770 | |||||||
| chr3:133425774 | AAAGGGAA others(4): Show |
A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(23): Show |
27 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-21535_490-2152 others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425774 | ||||||
| chr3:133425777 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.490-21540G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425777 | |||||||
| chr3:133425780 | AAAGGG | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(162): Show |
168 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.490-21518_490-2151 others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425780 | ||||||
| chr3:133425784 | G | GGAAGGGA others(6): Show |
12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-21531_490-2151 others(17): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425784 | ||||||
| chr3:133425785 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.490-21532G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425785 | |||||||
| chr3:133425785 | G | GAAAGGGA | 3 | a0001c0001t0001g0015 a0001c0001t0001g0137 a0001c0001t0001g0168 |
3 | HG02257.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.490-21530_490-2152 others(11): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425785 | ||||||
| chr3:133425785 | G | GAAAGGGA others(6): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0158 |
2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-21530_490-2152 others(17): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425785 | ||||||
| chr3:133425787 | A | AAG | 26 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
27 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-21530_490-2152 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425787 | |||||||
| chr3:133425788 | G | GGGAAGGG others(52): Show |
2 | a0001c0002t0001g0217 a0001c0002t0001g0226 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.490-21519_490-2151 others(63): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425788 | ||||||
| chr3:133425790 | G | A | 11 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0032 others(8): Show |
11 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-21527G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425790 | |||||||
| chr3:133425793 | G | A | 1 | a0002c0003t0001g0219 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.490-21524G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425793 | |||||||
| chr3:133425800 | GAAGAAGG others(21): Show |
G | 1 | a0001c0001t0001g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490-21516_490-2148 others(32): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425800 | |||||||
| chr3:133425803 | G | A | 1 | a0006c0009t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-21514G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425803 | |||||||
| chr3:133425804 | A | T | 1 | a0006c0009t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-21513A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425804 | |||||||
| chr3:133425806 | G | A | 1 | a0006c0009t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-21511G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425806 | |||||||
| chr3:133425807 | G | A | 1 | a0006c0009t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-21510G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425807 | |||||||
| chr3:133425807 | G | GGAAGGGA others(11): Show |
45 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(42): Show |
46 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.490-21483_490-2146 others(22): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425807 | ||||||
| chr3:133425807 | G | GGAAGGGA others(29): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0158 a0001c0001t0001g0212 |
3 | HG02109.hp2 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-21501_490-2146 others(40): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425807 | ||||||
| chr3:133425807 | GGAAGGGA others(11): Show |
G | 2 | a0001c0002t0001g0191 a0001c0002t0001g0220 |
2 | HG00735.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.490-21483_490-2146 others(22): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425807 | ||||||
| chr3:133425825 | A | AGAAGGGA others(16): Show |
1 | a0001c0001t0001g0193 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.490-21488_490-2146 others(27): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425825 | ||||||
| chr3:133425846 | A | C | 1 | a0001c0001t0001g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.490-21471A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425846 | |||||||
| chr3:133425853 | G | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(45): Show |
49 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.490-21464G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425853 | |||||||
| chr3:133425856 | A | C | 1 | a0001c0002t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.490-21461A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425856 | |||||||
| chr3:133425864 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-21453G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425864 | |||||||
| chr3:133425900 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.490-21417A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425900 | |||||||
| chr3:133425913 | G | GGGCAAGG others(3): Show |
18 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0022 others(15): Show |
19 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.490-21400_490-2139 others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425913 | ||||||
| chr3:133425943 | A | AGGCTAGG others(85): Show |
2 | a0001c0002t0001g0040 a0001c0002t0001g0192 |
2 | HG00735.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.490-21372_490-2137 others(96): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(90): Show |
11 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0072 others(8): Show |
12 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-21372_490-2137 others(101): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(79): Show |
1 | a0001c0001t0001g0212 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.490-21372_490-2137 others(90): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(90): Show |
5 | a0001c0001t0001g0026 a0001c0001t0001g0138 a0001c0001t0001g0162 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-21372_490-2137 others(101): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(101): Show |
7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0163 others(4): Show |
7 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-21372_490-2137 others(112): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(145): Show |
1 | a0001c0001t0001g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-21372_490-2137 others(156): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(97): Show |
1 | a0001c0001t0001g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490-21372_490-2137 others(108): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(80): Show |
1 | a0001c0001t0001g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490-21372_490-2137 others(91): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(73): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0158 |
2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-21372_490-2137 others(84): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(74): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0137 a0001c0001t0001g0168 |
3 | HG02257.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.490-21372_490-2137 others(85): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(69): Show |
18 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0044 others(15): Show |
18 | HG02055.hp1 HG02165.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.490-21372_490-2137 others(80): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(80): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0250 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-21372_490-2137 others(91): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(114): Show |
1 | a0001c0001t0001g0180 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.490-21372_490-2137 others(125): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGCTAGG others(77): Show |
1 | a0001c0001t0001g0070 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.490-21372_490-2137 others(88): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425943 | A | AGGGAGGG others(435): Show |
1 | a0001c0001t0001g0123 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.490-21366_490-2136 others(446): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425943 | ||||||
| chr3:133425946 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.490-21371G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425946 | |||||||
| chr3:133425952 | A | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0018 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.490-21365A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425952 | |||||||
| chr3:133425953 | G | A | 51 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0014 others(48): Show |
52 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.490-21364G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425953 | |||||||
| chr3:133425953 | G | GGGGGAAG others(81): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG02717.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.490-21359_490-2135 others(92): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(92): Show |
8 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
8 | HG02109.hp1 HG02970.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-21359_490-2135 others(103): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(150): Show |
1 | a0001c0002t0001g0221 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(161): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(145): Show |
2 | a0001c0001t0001g0152 a0001c0002t0001g0132 |
2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.490-21359_490-2135 others(156): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(151): Show |
1 | a0001c0002t0001g0175 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(162): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(162): Show |
3 | a0001c0001t0001g0056 a0001c0001t0001g0101 a0001c0002t0001g0252 |
3 | HG03669.hp1 NA18969.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.490-21359_490-2135 others(173): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(167): Show |
1 | a0001c0001t0001g0099 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(178): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(151): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0108 a0001c0001t0001g0189 others(7): Show |
11 | HG01255.hp2 HG02129.hp2 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-21359_490-2135 others(162): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(167): Show |
1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(178): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(140): Show |
1 | a0001c0008t0001g0125 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(151): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(152): Show |
1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(163): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(153): Show |
1 | a0001c0001t0001g0105 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(164): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(93): Show |
1 | a0001c0001t0001g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(104): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(154): Show |
1 | a0001c0002t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(165): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAAG others(163): Show |
1 | a0001c0002t0001g0049 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(174): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAGG others(574): Show |
1 | a0001c0001t0001g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490-21355_490-2135 others(585): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425953 | G | GGGGGAGG others(564): Show |
1 | a0001c0001t0001g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-21355_490-2135 others(575): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425953 | ||||||
| chr3:133425957 | G | A | 2 | a0001c0001t0001g0070 a0001c0002t0001g0183 |
2 | HG00738.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.490-21360G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425957 | |||||||
| chr3:133425957 | G | GGAAGTGG others(154): Show |
1 | a0001c0002t0001g0206 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.490-21360_490-2135 others(165): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425957 | |||||||
| chr3:133425958 | A | AAGTGGAG others(165): Show |
1 | a0001c0002t0001g0065 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(176): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425958 | |||||||
| chr3:133425958 | A | AAGTGGAG others(231): Show |
1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(242): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425958 | |||||||
| chr3:133425958 | A | AAGTGGAG others(152): Show |
1 | a0002c0007t0001g0243 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.490-21359_490-2135 others(163): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425958 | |||||||
| chr3:133425958 | A | AAGTGGAG others(164): Show |
1 | a0001c0002t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.490-21359_490-2135 others(175): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425958 | |||||||
| chr3:133425958 | A | AGTGGAGG others(148): Show |
1 | a0001c0002t0001g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.490-21358_490-2135 others(159): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425958 | ||||||
| chr3:133425958 | A | G | 1 | a0001c0002t0001g0206 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.490-21359A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425958 | |||||||
| chr3:133425959 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
146 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.490-21358G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425959 | |||||||
| chr3:133425959 | G | GGGGAGGG others(441): Show |
1 | a0002c0003t0001g0219 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.490-21355_490-2135 others(452): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425959 | ||||||
| chr3:133425959 | G | GGGGAGGG others(176): Show |
1 | a0001c0002t0001g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.490-21355_490-2135 others(187): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425959 | ||||||
| chr3:133425959 | G | GGGGGGAG others(511): Show |
1 | a0001c0001t0001g0186 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.490-21354_490-2135 others(522): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425959 | ||||||
| chr3:133425961 | G | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
146 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.490-21356G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425961 | |||||||
| chr3:133425963 | G | A | 24 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(21): Show |
24 | HG02055.hp1 HG02165.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-21354G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425963 | |||||||
| chr3:133425964 | A | AGGGGAGG others(503): Show |
1 | a0001c0001t0001g0188 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(514): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(505): Show |
1 | a0001c0001t0001g0062 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(516): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(498): Show |
1 | a0001c0001t0001g0214 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(509): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(510): Show |
1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(521): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(517): Show |
1 | a0001c0002t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(528): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(439): Show |
1 | a0001c0001t0001g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(450): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(406): Show |
1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(417): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(413): Show |
1 | a0001c0001t0001g0193 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(424): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(444): Show |
1 | a0001c0001t0001g0235 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(455): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(423): Show |
1 | a0001c0001t0001g0079 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(434): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(435): Show |
1 | a0001c0001t0001g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(446): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(384): Show |
1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(395): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(448): Show |
1 | a0001c0001t0001g0144 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(459): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(418): Show |
1 | a0001c0002t0001g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(429): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGAGG others(371): Show |
1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(382): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | AGGGGATG others(241): Show |
1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.490-21344_490-2134 others(252): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425964 | ||||||
| chr3:133425964 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.490-21353A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425964 | |||||||
| chr3:133425966 | G | GGGAGGGG others(506): Show |
1 | a0001c0001t0001g0239 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490-21348_490-2134 others(517): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425966 | ||||||
| chr3:133425968 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-21349G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425968 | |||||||
| chr3:133425969 | A | AGGGGGAG others(90): Show |
1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.490-21348_490-2134 others(101): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425969 | |||||||
| chr3:133425969 | A | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0069 others(4): Show |
7 | HG00099.hp2 HG01175.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-21348A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425969 | |||||||
| chr3:133425969 | AT | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(115): Show |
119 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.490-21347delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425969 | |||||||
| chr3:133425969 | ATG | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(70): Show |
75 | HG00423.hp1 HG00735.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.490-21347_490-2134 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425969 | |||||||
| chr3:133425970 | T | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0032 others(5): Show |
8 | HG00099.hp2 HG01175.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-21347T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425970 | |||||||
| chr3:133425970 | T | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(45): Show |
49 | HG00558.hp1 HG00738.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.490-21347T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425970 | |||||||
| chr3:133425971 | G | GGGA | 23 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(20): Show |
23 | HG02055.hp1 HG02165.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.490-21344_490-2134 others(7): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | ||||||
| chr3:133425971 | G | GGGGAGGG others(105): Show |
1 | a0001c0001t0001g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.490-21343_490-2134 others(116): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | ||||||
| chr3:133425971 | G | GGGGAGGG others(100): Show |
9 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0027 others(6): Show |
9 | HG02451.hp2 HG02572.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-21343_490-2134 others(111): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | ||||||
| chr3:133425971 | G | GGGGAGGG others(116): Show |
1 | a0001c0001t0001g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-21343_490-2134 others(127): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | ||||||
| chr3:133425971 | G | GGGGAGGG others(122): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG01243.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.490-21343_490-2134 others(133): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | ||||||
| chr3:133425971 | G | GGGGAGGG others(111): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0266 |
4 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-21343_490-2134 others(122): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | ||||||
| chr3:133425971 | G | GGGGAGGG others(151): Show |
1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-21343_490-2134 others(162): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | ||||||
| chr3:133425971 | G | GGGGAGGG others(52): Show |
1 | a0001c0001t0001g0254 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.490-21343_490-2134 others(63): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425971 | ||||||
| chr3:133425975 | G | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(22): Show |
25 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-21342G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425975 | |||||||
| chr3:133425980 | G | GAGGGGGA others(159): Show |
1 | a0001c0001t0001g0069 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(170): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(143): Show |
2 | a0001c0001t0001g0103 a0001c0001t0001g0230 |
2 | HG01081.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.490-21336_490-2133 others(154): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(127): Show |
1 | a0001c0001t0001g0074 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(138): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(154): Show |
7 | a0001c0001t0001g0053 a0001c0001t0001g0075 a0001c0001t0001g0076 others(4): Show |
7 | HG01255.hp1 HG01346.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-21336_490-2133 others(165): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(155): Show |
1 | a0001c0001t0001g0241 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(166): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(154): Show |
1 | a0001c0001t0001g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(165): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(84): Show |
2 | a0001c0002t0001g0111 a0001c0002t0001g0240 |
2 | NA18962.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.490-21336_490-2133 others(95): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(150): Show |
1 | a0001c0001t0001g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(161): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(159): Show |
1 | a0001c0001t0001g0146 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(170): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(203): Show |
1 | a0001c0001t0001g0102 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(214): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(188): Show |
1 | a0001c0002t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(199): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(171): Show |
9 | a0001c0001t0001g0043 a0001c0001t0001g0095 a0001c0001t0001g0157 others(6): Show |
9 | HG00558.hp2 HG00621.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-21336_490-2133 others(182): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(172): Show |
1 | a0001c0002t0001g0045 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(183): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(155): Show |
1 | a0001c0001t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(166): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(172): Show |
1 | a0001c0001t0001g0198 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(183): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(208): Show |
1 | a0001c0001t0001g0046 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(219): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(192): Show |
1 | a0001c0002t0001g0159 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(203): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(160): Show |
62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(59): Show |
63 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.490-21336_490-2133 others(171): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(165): Show |
1 | a0001c0002t0001g0050 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(176): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(181): Show |
4 | a0001c0001t0001g0085 a0001c0001t0001g0106 a0001c0001t0001g0205 others(1): Show |
4 | NA18946.hp2 NA18956.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-21336_490-2133 others(192): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(161): Show |
1 | a0001c0001t0001g0190 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(161): Show |
1 | a0001c0002t0001g0220 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(144): Show |
1 | a0001c0002t0001g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(155): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(149): Show |
1 | a0001c0001t0001g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(160): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(161): Show |
1 | a0001c0002t0001g0064 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(161): Show |
1 | a0001c0002t0001g0215 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(171): Show |
3 | a0001c0001t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0116 |
3 | NA18960.hp2 NA18983.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.490-21336_490-2133 others(182): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(161): Show |
2 | a0001c0002t0001g0039 a0001c0002t0001g0080 |
2 | HG00438.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(149): Show |
1 | a0001c0002t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(160): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(161): Show |
1 | a0001c0001t0001g0231 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(172): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(176): Show |
2 | a0001c0002t0001g0177 a0001c0002t0001g0178 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.490-21336_490-2133 others(187): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(162): Show |
1 | a0001c0002t0001g0191 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(173): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(166): Show |
1 | a0001c0002t0001g0257 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(177): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(162): Show |
1 | a0001c0002t0001g0121 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(173): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGA others(162): Show |
1 | a0001c0002t0001g0234 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(173): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGG others(155): Show |
1 | a0001c0001t0001g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(166): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGG others(168): Show |
1 | a0001c0002t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490-21336_490-2133 others(179): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GAGGGGGG others(173): Show |
1 | a0001c0002t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.490-21336_490-2133 others(184): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425980 | ||||||
| chr3:133425980 | G | GGAGGGGG others(168): Show |
1 | a0001c0002t0001g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.490-21337_490-2133 others(179): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425980 | |||||||
| chr3:133425981 | A | G | 2 | a0001c0001t0001g0097 a0001c0002t0001g0035 |
2 | HG01175.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.490-21336A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425981 | |||||||
| chr3:133425982 | A | AGGGGAGG others(504): Show |
1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-21333_490-2133 others(515): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425982 | ||||||
| chr3:133425982 | A | AGGGGGAG others(193): Show |
1 | a0001c0001t0001g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.490-21333_490-2133 others(204): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425982 | ||||||
| chr3:133425982 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.490-21335A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425982 | |||||||
| chr3:133425983 | G | GGGGGAGG others(460): Show |
1 | a0001c0001t0001g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.490-21333_490-2133 others(471): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425983 | ||||||
| chr3:133425985 | C | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.490-21332C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425985 | |||||||
| chr3:133425985 | C | CAGGGCAG others(3): Show |
2 | a0001c0002t0001g0183 a0001c0002t0001g0206 |
2 | HG00423.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.490-21323_490-2132 others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425985 | ||||||
| chr3:133425985 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490-21332C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425985 | |||||||
| chr3:133425987 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490-21330G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425987 | |||||||
| chr3:133425991 | A | AGGGAAGG others(4): Show |
2 | a0001c0001t0001g0105 a0002c0007t0001g0243 |
2 | HG02273.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.490-21323_490-2132 others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133425991 | ||||||
| chr3:133425994 | G | T | 1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.490-21323G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425994 | |||||||
| chr3:133425995 | C | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0099 others(23): Show |
27 | HG01255.hp2 HG02056.hp1 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-21322C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425995 | |||||||
| chr3:133425995 | C | G | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-21322C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133425995 | |||||||
| chr3:133426000 | C | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.490-21317C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426000 | |||||||
| chr3:133426002 | G | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.490-21315G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426002 | |||||||
| chr3:133426004 | G | GCAGGGCA others(33): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0099 others(20): Show |
24 | HG01255.hp2 HG02056.hp1 HG02129.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-21313_490-2131 others(44): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426004 | |||||||
| chr3:133426004 | G | GCAGGGCA others(43): Show |
2 | a0001c0001t0001g0224 a0001c0001t0001g0228 |
2 | NA18964.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.490-21313_490-2131 others(54): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426004 | |||||||
| chr3:133426004 | G | GGCAGGGC others(36): Show |
1 | a0001c0002t0001g0065 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.490-21313_490-2131 others(47): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426004 | |||||||
| chr3:133426005 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-21312A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426005 | |||||||
| chr3:133426007 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(46): Show |
50 | HG01123.hp2 HG01175.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.490-21310A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426007 | |||||||
| chr3:133426007 | AGGAAG | A | 6 | a0001c0001t0001g0079 a0001c0001t0001g0127 a0001c0001t0001g0193 others(3): Show |
6 | HG00621.hp2 HG02015.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-21280_490-2127 others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426007 | ||||||
| chr3:133426014 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0099 others(23): Show |
27 | HG01255.hp2 HG02056.hp1 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-21303G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426014 | |||||||
| chr3:133426014 | G | GAAGGAAA others(18): Show |
21 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(18): Show |
21 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.490-21299_490-2129 others(29): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426014 | ||||||
| chr3:133426014 | G | GAAGGGAA others(23): Show |
193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(190): Show |
196 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.490-21294_490-2129 others(34): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426014 | ||||||
| chr3:133426019 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-21298G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426019 | |||||||
| chr3:133426022 | G | A | 1 | a0001c0002t0001g0065 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.490-21295G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426022 | |||||||
| chr3:133426024 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(233): Show |
241 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.490-21293G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426024 | |||||||
| chr3:133426025 | A | AAGGGAAA others(24): Show |
1 | a0001c0002t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.490-21286_490-2128 others(35): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426025 | ||||||
| chr3:133426026 | A | AGGAAAGA others(23): Show |
1 | a0001c0002t0001g0215 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.490-21289_490-2128 others(34): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426026 | ||||||
| chr3:133426026 | A | AGGGAAAG others(24): Show |
1 | a0001c0001t0001g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490-21286_490-2128 others(35): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133426026 | ||||||
| chr3:133426032 | G | A | 1 | a0001c0002t0001g0065 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.490-21285G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426032 | |||||||
| chr3:133426055 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-21262G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426055 | |||||||
| chr3:133426095 | C | T | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-21222C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426095 | |||||||
| chr3:133426102 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-21215C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426102 | |||||||
| chr3:133426103 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-21214A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426103 | |||||||
| chr3:133426184 | C | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0138 a0002c0003t0001g0145 |
3 | HG02280.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.490-21133C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426184 | |||||||
| chr3:133426298 | G | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0137 a0001c0001t0001g0168 |
3 | HG02257.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.490-21019G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426298 | |||||||
| chr3:133426308 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490-21009A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426308 | |||||||
| chr3:133426436 | A | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.490-20881A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426436 | |||||||
| chr3:133426451 | A | G | 7 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(4): Show |
7 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-20866A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426451 | |||||||
| chr3:133426486 | G | C | 34 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(31): Show |
35 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.490-20831G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426486 | |||||||
| chr3:133426615 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.490-20702G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426615 | |||||||
| chr3:133426624 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490-20693T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426624 | |||||||
| chr3:133426625 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490-20692C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426625 | |||||||
| chr3:133426646 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.490-20671C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426646 | |||||||
| chr3:133426727 | T | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(22): Show |
25 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-20590T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426727 | |||||||
| chr3:133426743 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
237 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.490-20574A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426743 | |||||||
| chr3:133426762 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-20555G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426762 | |||||||
| chr3:133426911 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.490-20406T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426911 | |||||||
| chr3:133426926 | G | T | 1 | a0001c0001t0001g0190 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.490-20391G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426926 | |||||||
| chr3:133426945 | T | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG01243.hp2 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.490-20372T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133426945 | |||||||
| chr3:133427028 | C | A | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG01243.hp2 HG03471.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-20289C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427028 | |||||||
| chr3:133427117 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.490-20200C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427117 | |||||||
| chr3:133427379 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
265 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.490-19938G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427379 | |||||||
| chr3:133427403 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.490-19914G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427403 | |||||||
| chr3:133427514 | T | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(22): Show |
25 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-19803T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427514 | |||||||
| chr3:133427517 | A | T | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.490-19800A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427517 | |||||||
| chr3:133427578 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.490-19739C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427578 | |||||||
| chr3:133427585 | C | A | 1 | a0001c0002t0001g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.490-19732C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427585 | |||||||
| chr3:133427683 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.490-19634C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427683 | |||||||
| chr3:133427696 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.490-19621T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427696 | |||||||
| chr3:133427705 | C | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0022 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-19612C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427705 | |||||||
| chr3:133427818 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.490-19499A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427818 | |||||||
| chr3:133427941 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.490-19376A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133427941 | |||||||
| chr3:133428016 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.490-19301A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428016 | |||||||
| chr3:133428061 | T | C | 1 | a0001c0002t0002g0225 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.490-19256T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428061 | |||||||
| chr3:133428226 | C | G | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(44): Show |
48 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-19091C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428226 | |||||||
| chr3:133428240 | G | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(22): Show |
25 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-19077G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428240 | |||||||
| chr3:133428257 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.490-19060C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428257 | |||||||
| chr3:133428277 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0022 others(16): Show |
20 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-19040G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428277 | |||||||
| chr3:133428282 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.490-19035A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428282 | |||||||
| chr3:133428289 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.490-19028A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428289 | |||||||
| chr3:133428331 | G | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(22): Show |
25 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-18986G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428331 | |||||||
| chr3:133428334 | AG | A | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(44): Show |
48 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-18980delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133428334 | ||||||
| chr3:133428339 | G | A | 16 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0026 others(13): Show |
17 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-18978G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428339 | |||||||
| chr3:133428384 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(239): Show |
247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.490-18933A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428384 | |||||||
| chr3:133428431 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.490-18886A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428431 | |||||||
| chr3:133428482 | C | CA | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
221 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.490-18824dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133428482 | ||||||
| chr3:133428498 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-18819A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428498 | |||||||
| chr3:133428592 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-18725G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428592 | |||||||
| chr3:133428657 | GA | G | 16 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0026 others(13): Show |
17 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-18657delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133428657 | ||||||
| chr3:133428673 | T | A | 1 | a0001c0002t0001g0233 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.490-18644T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428673 | |||||||
| chr3:133428769 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0023 |
2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.490-18548C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428769 | |||||||
| chr3:133428796 | C | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
250 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.490-18521C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428796 | |||||||
| chr3:133428803 | G | A | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(44): Show |
48 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-18514G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428803 | |||||||
| chr3:133428805 | C | T | 1 | a0001c0002t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.490-18512C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428805 | |||||||
| chr3:133428824 | C | A | 1 | a0001c0001t0001g0190 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.490-18493C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428824 | |||||||
| chr3:133428825 | C | T | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(44): Show |
48 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-18492C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428825 | |||||||
| chr3:133428875 | C | T | 3 | a0001c0002t0001g0077 a0001c0002t0001g0090 a0001c0002t0001g0216 |
3 | NA18952.hp2 NA19063.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.490-18442C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428875 | |||||||
| chr3:133428876 | C | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.490-18441C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428876 | |||||||
| chr3:133428945 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.490-18372C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133428945 | |||||||
| chr3:133429022 | T | TA | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(171): Show |
177 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.490-18289dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133429022 | ||||||
| chr3:133429030 | C | T | 2 | a0001c0001t0001g0014 a0001c0002t0001g0177 |
2 | HG01517.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.490-18287C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429030 | |||||||
| chr3:133429110 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490-18207C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429110 | |||||||
| chr3:133429111 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490-18206A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429111 | |||||||
| chr3:133429116 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.490-18201C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429116 | |||||||
| chr3:133429118 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-18199C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429118 | |||||||
| chr3:133429136 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490-18181T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429136 | |||||||
| chr3:133429286 | T | G | 1 | a0001c0001t0001g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490-18031T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429286 | |||||||
| chr3:133429326 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0137 a0001c0001t0001g0168 |
3 | HG02257.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.490-17991G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429326 | |||||||
| chr3:133429379 | T | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.490-17938T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429379 | |||||||
| chr3:133429391 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.490-17926A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429391 | |||||||
| chr3:133429498 | A | G | 60 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(57): Show |
62 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.490-17819A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429498 | |||||||
| chr3:133429507 | C | T | 1 | a0001c0002t0001g0179 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.490-17810C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429507 | |||||||
| chr3:133429574 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.490-17743G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429574 | |||||||
| chr3:133429659 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.490-17658G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429659 | |||||||
| chr3:133429765 | T | TA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(32): Show |
36 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.490-17552_490-1755 others(5): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429765 | |||||||
| chr3:133429765 | T | TTA | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(198): Show |
205 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.490-17551_490-1755 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133429765 | ||||||
| chr3:133429774 | C | T | 1 | a0001c0002t0001g0045 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.490-17543C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429774 | |||||||
| chr3:133429803 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.490-17514G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429803 | |||||||
| chr3:133429828 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-17489A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429828 | |||||||
| chr3:133429838 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.490-17479T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429838 | |||||||
| chr3:133429897 | C | A | 1 | a0006c0009t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-17420C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429897 | |||||||
| chr3:133429904 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.490-17413A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429904 | |||||||
| chr3:133429907 | A | AC | 21 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0042 others(18): Show |
21 | HG00738.hp1 HG01106.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.490-17405dupC | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133429907 | ||||||
| chr3:133429907 | A | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17410A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429907 | |||||||
| chr3:133429920 | A | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17397A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429920 | |||||||
| chr3:133429925 | T | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17392T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429925 | |||||||
| chr3:133429929 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17388C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429929 | |||||||
| chr3:133429934 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(10): Show |
13 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-17383C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429934 | |||||||
| chr3:133429947 | T | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17370T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429947 | |||||||
| chr3:133429959 | T | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17358T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429959 | |||||||
| chr3:133429964 | T | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17353T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429964 | |||||||
| chr3:133429967 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.490-17350C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429967 | |||||||
| chr3:133429976 | A | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17341A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133429976 | |||||||
| chr3:133430001 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17316C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430001 | |||||||
| chr3:133430010 | G | C | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-17307G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430010 | |||||||
| chr3:133430015 | T | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17302T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430015 | |||||||
| chr3:133430024 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(238): Show |
246 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.490-17293T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430024 | |||||||
| chr3:133430025 | G | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-17292G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430025 | |||||||
| chr3:133430027 | T | C | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-17290T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430027 | |||||||
| chr3:133430063 | T | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0022 others(11): Show |
15 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-17254T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430063 | |||||||
| chr3:133430114 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-17203C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430114 | |||||||
| chr3:133430192 | T | G | 2 | a0001c0002t0001g0039 a0001c0002t0001g0080 |
2 | HG00438.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.490-17125T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430192 | |||||||
| chr3:133430236 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0137 |
2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490-17081A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430236 | |||||||
| chr3:133430250 | T | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0022 others(11): Show |
15 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-17067T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430250 | |||||||
| chr3:133430291 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.490-17026A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430291 | |||||||
| chr3:133430292 | A | C | 15 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0026 others(12): Show |
16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-17025A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430292 | |||||||
| chr3:133430315 | C | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0026 others(12): Show |
16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-17002C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430315 | |||||||
| chr3:133430345 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(239): Show |
247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.490-16972C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430345 | |||||||
| chr3:133430391 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-16926A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430391 | |||||||
| chr3:133430517 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.490-16800G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430517 | |||||||
| chr3:133430533 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.490-16784T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430533 | |||||||
| chr3:133430565 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.490-16752G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430565 | |||||||
| chr3:133430626 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-16691G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430626 | |||||||
| chr3:133430634 | G | A | 2 | a0001c0001t0001g0235 a0002c0003t0001g0115 |
2 | HG02071.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.490-16683G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430634 | |||||||
| chr3:133430642 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.490-16675C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430642 | |||||||
| chr3:133430691 | A | G | 15 | a0001c0001t0001g0053 a0001c0001t0001g0066 a0001c0001t0001g0075 others(12): Show |
15 | HG01081.hp1 HG01255.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.490-16626A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430691 | |||||||
| chr3:133430692 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.490-16625T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430692 | |||||||
| chr3:133430694 | C | A | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(44): Show |
48 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-16623C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430694 | |||||||
| chr3:133430695 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(217): Show |
225 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.490-16622A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430695 | |||||||
| chr3:133430761 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG01243.hp2 HG02622.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-16556G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430761 | |||||||
| chr3:133430793 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.490-16524A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430793 | |||||||
| chr3:133430837 | C | T | 10 | a0001c0001t0001g0052 a0001c0001t0001g0101 a0001c0001t0001g0102 others(7): Show |
10 | HG01070.hp2 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-16480C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430837 | |||||||
| chr3:133430841 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.490-16476C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430841 | |||||||
| chr3:133430862 | C | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0266 |
4 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-16455C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430862 | |||||||
| chr3:133430873 | C | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(13): Show |
17 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-16444C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430873 | |||||||
| chr3:133430884 | T | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
14 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-16433T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430884 | |||||||
| chr3:133430939 | C | A | 1 | a0001c0001t0001g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.490-16378C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133430939 | |||||||
| chr3:133431063 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0105 |
2 | HG01993.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.490-16254C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431063 | |||||||
| chr3:133431067 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.490-16250G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431067 | |||||||
| chr3:133431077 | TGGTTCGT others(2): Show |
T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.490-16237_490-1622 others(13): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133431077 | ||||||
| chr3:133431104 | G | A | 26 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(23): Show |
26 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-16213G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431104 | |||||||
| chr3:133431140 | G | A | 26 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(23): Show |
26 | HG00738.hp1 HG02055.hp1 HG02165.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-16177G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431140 | |||||||
| chr3:133431347 | A | G | 1 | a0001c0002t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.490-15970A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431347 | |||||||
| chr3:133431394 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(150): Show |
155 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.490-15923G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431394 | |||||||
| chr3:133431442 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
242 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.490-15875C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431442 | |||||||
| chr3:133431484 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-15833G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431484 | |||||||
| chr3:133431535 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.490-15782C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431535 | |||||||
| chr3:133431607 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0212 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-15710G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431607 | |||||||
| chr3:133431611 | G | A | 118 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0051 others(115): Show |
118 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.490-15706G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431611 | |||||||
| chr3:133431643 | C | T | 39 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(36): Show |
40 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.490-15674C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431643 | |||||||
| chr3:133431666 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
237 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.490-15651C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431666 | |||||||
| chr3:133431677 | T | C | 2 | a0001c0001t0001g0107 a0001c0002t0001g0035 |
2 | HG03239.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.490-15640T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431677 | |||||||
| chr3:133431680 | A | G | 2 | a0001c0001t0001g0107 a0001c0002t0001g0035 |
2 | HG03239.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.490-15637A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431680 | |||||||
| chr3:133431698 | C | CG | 4 | a0001c0001t0001g0148 a0001c0001t0001g0212 a0001c0002t0001g0057 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-15618dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133431698 | ||||||
| chr3:133431698 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.490-15619C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431698 | |||||||
| chr3:133431712 | C | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(11): Show |
15 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.490-15605C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431712 | |||||||
| chr3:133431735 | T | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(17): Show |
20 | HG00738.hp1 HG02055.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-15582T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431735 | |||||||
| chr3:133431738 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(16): Show |
19 | HG00738.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.490-15579A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431738 | |||||||
| chr3:133431777 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(8): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-15540C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431777 | |||||||
| chr3:133431806 | A | T | 23 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0022 others(20): Show |
23 | HG00738.hp1 HG01243.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.490-15511A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431806 | |||||||
| chr3:133431831 | C | T | 70 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(67): Show |
70 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.490-15486C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431831 | |||||||
| chr3:133431845 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0212 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-15472C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431845 | |||||||
| chr3:133431869 | C | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
12 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-15448C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431869 | |||||||
| chr3:133431978 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(188): Show |
195 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.490-15339G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431978 | |||||||
| chr3:133431989 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.490-15328A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431989 | |||||||
| chr3:133431998 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0212 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-15319C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133431998 | |||||||
| chr3:133432010 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.490-15307C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432010 | |||||||
| chr3:133432019 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(188): Show |
195 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.490-15298A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432019 | |||||||
| chr3:133432021 | C | CATCT | 5 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-15295_490-1529 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133432021 | ||||||
| chr3:133432094 | T | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(233): Show |
241 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.490-15223T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432094 | |||||||
| chr3:133432097 | C | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0025 |
2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.490-15220C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432097 | |||||||
| chr3:133432100 | C | T | 11 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0163 others(8): Show |
11 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-15217C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432100 | |||||||
| chr3:133432124 | G | A | 17 | a0001c0001t0001g0053 a0001c0001t0001g0066 a0001c0001t0001g0075 others(14): Show |
17 | HG01081.hp1 HG01255.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.490-15193G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432124 | |||||||
| chr3:133432259 | C | T | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-15058C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432259 | |||||||
| chr3:133432307 | C | A | 2 | a0001c0002t0001g0055 a0001c0002t0001g0098 |
2 | NA18973.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.490-15010C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432307 | |||||||
| chr3:133432574 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0212 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-14743A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432574 | |||||||
| chr3:133432821 | G | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.490-14496G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432821 | |||||||
| chr3:133432833 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-14484C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432833 | |||||||
| chr3:133432834 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0212 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-14483G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432834 | |||||||
| chr3:133432867 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-14450T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432867 | |||||||
| chr3:133432869 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-14448C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432869 | |||||||
| chr3:133432872 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-14445C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432872 | |||||||
| chr3:133432926 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.490-14391C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432926 | |||||||
| chr3:133432955 | C | G | 35 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(32): Show |
35 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.490-14362C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133432955 | |||||||
| chr3:133433051 | A | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0117 others(1): Show |
4 | HG01993.hp1 HG02273.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-14266A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433051 | |||||||
| chr3:133433221 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.490-14096A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433221 | |||||||
| chr3:133433266 | T | C | 1 | a0001c0002t0001g0091 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.490-14051T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433266 | |||||||
| chr3:133433412 | C | A | 1 | a0001c0002t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490-13905C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433412 | |||||||
| chr3:133433421 | G | A | 1 | a0001c0002t0001g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.490-13896G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433421 | |||||||
| chr3:133433433 | A | C | 1 | a0001c0002t0001g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.490-13884A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433433 | |||||||
| chr3:133433450 | C | G | 1 | a0001c0001t0001g0228 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.490-13867C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433450 | |||||||
| chr3:133433455 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.490-13862T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433455 | |||||||
| chr3:133433456 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.490-13861C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433456 | |||||||
| chr3:133433461 | T | C | 2 | a0001c0002t0001g0176 a0001c0002t0001g0270 |
2 | HG01167.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.490-13856T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433461 | |||||||
| chr3:133433469 | A | G | 2 | a0001c0002t0001g0035 a0001c0002t0001g0045 |
2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.490-13848A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433469 | |||||||
| chr3:133433707 | C | G | 2 | a0001c0002t0001g0035 a0001c0002t0001g0045 |
2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.490-13610C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433707 | |||||||
| chr3:133433775 | C | G | 24 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0079 others(21): Show |
24 | HG00621.hp2 HG01175.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.490-13542C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433775 | |||||||
| chr3:133433871 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0002t0001g0185 others(2): Show |
5 | HG00423.hp2 HG00597.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-13446G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133433871 | |||||||
| chr3:133434026 | A | G | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
130 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.490-13291A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434026 | |||||||
| chr3:133434197 | A | G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(101): Show |
105 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.490-13120A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434197 | |||||||
| chr3:133434237 | C | T | 35 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(32): Show |
35 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.490-13080C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434237 | |||||||
| chr3:133434278 | G | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0162 a0001c0001t0001g0163 others(5): Show |
8 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-13039G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434278 | |||||||
| chr3:133434328 | T | A | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(101): Show |
105 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.490-12989T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434328 | |||||||
| chr3:133434347 | T | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(79): Show |
83 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.490-12970T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434347 | |||||||
| chr3:133434437 | G | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
12 | HG00738.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-12880G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434437 | |||||||
| chr3:133434523 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.490-12794A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434523 | |||||||
| chr3:133434646 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-12671C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434646 | |||||||
| chr3:133434647 | A | G | 64 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(61): Show |
64 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.490-12670A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434647 | |||||||
| chr3:133434706 | T | C | 22 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(19): Show |
22 | HG00738.hp1 HG01243.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.490-12611T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434706 | |||||||
| chr3:133434760 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-12557T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434760 | |||||||
| chr3:133434761 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-12556A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133434761 | |||||||
| chr3:133435325 | A | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0026 others(11): Show |
15 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.490-11992A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435325 | |||||||
| chr3:133435331 | C | G | 1 | a0001c0001t0001g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.490-11986C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435331 | |||||||
| chr3:133435410 | C | A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
41 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.490-11907C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435410 | |||||||
| chr3:133435612 | C | G | 7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-11705C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435612 | |||||||
| chr3:133435755 | T | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0070 others(1): Show |
4 | HG00738.hp1 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-11562T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435755 | |||||||
| chr3:133435807 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.490-11510A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435807 | |||||||
| chr3:133435914 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-11403G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133435914 | |||||||
| chr3:133436048 | G | T | 1 | a0001c0001t0001g0171 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.490-11269G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436048 | |||||||
| chr3:133436062 | G | A | 1 | a0001c0002t0001g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.490-11255G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436062 | |||||||
| chr3:133436130 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(34): Show |
38 | HG00621.hp2 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.490-11187G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436130 | |||||||
| chr3:133436292 | C | G | 40 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(37): Show |
40 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.490-11025C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436292 | |||||||
| chr3:133436325 | C | CA | 35 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(32): Show |
35 | HG00438.hp1 HG00438.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.490-10971dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436325 | ||||||
| chr3:133436325 | C | CAA | 36 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0026 others(33): Show |
36 | HG00099.hp2 HG00738.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.490-10972_490-1097 others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436325 | ||||||
| chr3:133436325 | C | CAAA | 28 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(25): Show |
29 | HG00558.hp2 HG00621.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.490-10973_490-1097 others(7): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436325 | ||||||
| chr3:133436325 | C | CAAAA | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0043 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-10974_490-1097 others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436325 | ||||||
| chr3:133436325 | C | CAAAAA | 9 | a0001c0001t0001g0032 a0001c0001t0001g0163 a0001c0001t0001g0164 others(6): Show |
9 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-10975_490-1097 others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436325 | ||||||
| chr3:133436348 | C | A | 1 | a0001c0002t0001g0234 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.490-10969C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436348 | |||||||
| chr3:133436465 | T | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0094 a0001c0001t0001g0105 others(4): Show |
7 | HG01993.hp1 HG02273.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-10852T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436465 | |||||||
| chr3:133436477 | G | C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(9): Show |
12 | HG00738.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.490-10840G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436477 | |||||||
| chr3:133436664 | G | T | 13 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0032 others(10): Show |
13 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-10653G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436664 | |||||||
| chr3:133436704 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0212 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.490-10613C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436704 | |||||||
| chr3:133436754 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(24): Show |
28 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.490-10563G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436754 | |||||||
| chr3:133436754 | G | C | 13 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0032 others(10): Show |
13 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-10563G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436754 | |||||||
| chr3:133436765 | C | T | 1 | a0001c0002t0001g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.490-10552C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436765 | |||||||
| chr3:133436829 | A | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
263 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.490-10488A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133436829 | |||||||
| chr3:133436924 | AG | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(37): Show |
40 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.490-10391delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133436924 | ||||||
| chr3:133437472 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.490-9845G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437472 | |||||||
| chr3:133437479 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(9): Show |
12 | HG01884.hp1 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.490-9838C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437479 | |||||||
| chr3:133437545 | A | G | 2 | a0001c0002t0001g0035 a0001c0002t0001g0045 |
2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.490-9772A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437545 | |||||||
| chr3:133437629 | AAAAG | A | 22 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0097 others(19): Show |
22 | HG00621.hp2 HG01099.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.490-9681_490-9678d others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133437629 | ||||||
| chr3:133437664 | GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490-9638_490-9629d others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133437664 | ||||||
| chr3:133437770 | C | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0023 others(18): Show |
21 | HG00738.hp1 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.490-9547C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437770 | |||||||
| chr3:133437848 | C | T | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
102 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.490-9469C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437848 | |||||||
| chr3:133437853 | C | A | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0149 others(1): Show |
4 | HG02451.hp1 HG02922.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-9464C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133437853 | |||||||
| chr3:133438082 | T | C | 1 | a0001c0002t0001g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.490-9235T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438082 | |||||||
| chr3:133438262 | C | T | 34 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(31): Show |
34 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.490-9055C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438262 | |||||||
| chr3:133438324 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.490-8993C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438324 | |||||||
| chr3:133438398 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.490-8919G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438398 | |||||||
| chr3:133438481 | G | A | 1 | a0001c0002t0001g0233 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.490-8836G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438481 | |||||||
| chr3:133438492 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490-8825A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438492 | |||||||
| chr3:133438497 | T | C | 29 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(26): Show |
29 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.490-8820T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438497 | |||||||
| chr3:133438502 | T | C | 65 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(62): Show |
66 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.490-8815T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438502 | |||||||
| chr3:133438589 | C | T | 68 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(65): Show |
69 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.490-8728C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438589 | |||||||
| chr3:133438722 | T | C | 20 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0097 others(17): Show |
20 | HG01175.hp2 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-8595T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438722 | |||||||
| chr3:133438778 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.490-8539C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438778 | |||||||
| chr3:133438849 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.490-8468G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438849 | |||||||
| chr3:133438857 | G | C | 2 | a0001c0002t0001g0087 a0001c0002t0001g0192 |
2 | HG00735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.490-8460G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133438857 | |||||||
| chr3:133439142 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.490-8175T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439142 | |||||||
| chr3:133439200 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.490-8117T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439200 | |||||||
| chr3:133439493 | T | C | 1 | a0001c0002t0001g0263 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.490-7824T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439493 | |||||||
| chr3:133439520 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0212 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-7797A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439520 | |||||||
| chr3:133439578 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0133 others(3): Show |
6 | HG01884.hp1 HG02717.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-7739G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439578 | |||||||
| chr3:133439664 | G | A | 94 | a0001c0001t0001g0052 a0001c0001t0001g0101 a0001c0001t0001g0102 others(91): Show |
94 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.490-7653G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439664 | |||||||
| chr3:133439815 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-7502C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439815 | |||||||
| chr3:133439816 | G | A | 1 | a0001c0002t0001g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.490-7501G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439816 | |||||||
| chr3:133439825 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0130 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-7492C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439825 | |||||||
| chr3:133439838 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.490-7479A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439838 | |||||||
| chr3:133439928 | C | CAG | 26 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(23): Show |
27 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.490-7373_490-7372d others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133439928 | ||||||
| chr3:133439928 | C | G | 35 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(32): Show |
35 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.490-7389C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439928 | |||||||
| chr3:133439932 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0036 others(3): Show |
7 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-7385G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439932 | |||||||
| chr3:133439989 | G | A | 129 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0020 others(126): Show |
130 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.490-7328G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439989 | |||||||
| chr3:133439990 | T | G | 1 | a0001c0002t0001g0065 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.490-7327T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133439990 | |||||||
| chr3:133440048 | T | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(24): Show |
27 | HG01175.hp2 HG01243.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.490-7269T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440048 | |||||||
| chr3:133440197 | C | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0268 |
2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.490-7120C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440197 | |||||||
| chr3:133440211 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-7106G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440211 | |||||||
| chr3:133440226 | CATGATTC others(1): Show |
C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.490-7080_490-7073d others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133440226 | ||||||
| chr3:133440384 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.490-6933T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440384 | |||||||
| chr3:133440661 | A | G | 3 | a0002c0003t0001g0003 a0002c0003t0001g0154 a0002c0003t0001g0261 |
4 | HG01069.hp2 HG01071.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-6656A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440661 | |||||||
| chr3:133440754 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.490-6563C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440754 | |||||||
| chr3:133440873 | G | A | 2 | a0001c0002t0001g0028 a0001c0002t0001g0054 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.490-6444G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133440873 | |||||||
| chr3:133441039 | C | CT | 28 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0051 others(25): Show |
28 | HG00735.hp1 HG01175.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.490-6259dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133441039 | ||||||
| chr3:133441039 | C | CTT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(23): Show |
26 | HG01175.hp2 HG01243.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.490-6260_490-6259d others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133441039 | ||||||
| chr3:133441039 | CT | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0018 others(15): Show |
18 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.490-6259delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133441039 | ||||||
| chr3:133441250 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 |
3 | HG02109.hp1 HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.490-6067G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133441250 | |||||||
| chr3:133441696 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.490-5621G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133441696 | |||||||
| chr3:133441750 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-5567G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133441750 | |||||||
| chr3:133441803 | A | G | 1 | a0001c0002t0001g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.490-5514A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133441803 | |||||||
| chr3:133441809 | C | T | 4 | a0001c0002t0001g0037 a0001c0002t0001g0087 a0001c0002t0001g0192 others(1): Show |
4 | HG00735.hp2 HG01891.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-5508C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133441809 | |||||||
| chr3:133442033 | A | G | 1 | a0001c0002t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-5284A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442033 | |||||||
| chr3:133442067 | G | C | 149 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0014 others(146): Show |
150 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.490-5250G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442067 | |||||||
| chr3:133442353 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
14 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.490-4964C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442353 | |||||||
| chr3:133442385 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-4932G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442385 | |||||||
| chr3:133442449 | C | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0143 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-4868C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442449 | |||||||
| chr3:133442611 | T | C | 1 | a0002c0003t0001g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.490-4706T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442611 | |||||||
| chr3:133442627 | G | T | 66 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
66 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.490-4690G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442627 | |||||||
| chr3:133442839 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.490-4478T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442839 | |||||||
| chr3:133442862 | C | CT | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(2): Show |
5 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-4441dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133442862 | ||||||
| chr3:133442862 | CT | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-4441delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133442862 | ||||||
| chr3:133442920 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0169 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.490-4397C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133442920 | |||||||
| chr3:133443005 | G | A | 19 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0074 others(16): Show |
19 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-4312G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443005 | |||||||
| chr3:133443079 | G | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(34): Show |
37 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.490-4238G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443079 | |||||||
| chr3:133443289 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-4028T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443289 | |||||||
| chr3:133443295 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(30): Show |
34 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.490-4022T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443295 | |||||||
| chr3:133443387 | T | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
71 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.490-3930T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443387 | |||||||
| chr3:133443476 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.490-3841G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443476 | |||||||
| chr3:133443576 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.490-3741G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443576 | |||||||
| chr3:133443590 | G | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0066 others(15): Show |
19 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-3727G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133443590 | |||||||
| chr3:133444070 | A | G | 14 | a0001c0001t0001g0062 a0001c0001t0001g0072 a0001c0001t0001g0073 others(11): Show |
14 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-3247A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444070 | |||||||
| chr3:133444284 | G | A | 6 | a0001c0001t0001g0066 a0001c0001t0001g0075 a0001c0001t0001g0076 others(3): Show |
6 | HG01081.hp1 HG01346.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-3033G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444284 | |||||||
| chr3:133444480 | A | G | 19 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0074 others(16): Show |
19 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-2837A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444480 | |||||||
| chr3:133444498 | C | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(34): Show |
37 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.490-2819C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444498 | |||||||
| chr3:133444556 | G | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0027 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2761G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444556 | |||||||
| chr3:133444647 | C | T | 16 | a0001c0001t0001g0062 a0001c0001t0001g0072 a0001c0001t0001g0073 others(13): Show |
16 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-2670C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444647 | |||||||
| chr3:133444777 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.490-2540G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444777 | |||||||
| chr3:133444781 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490-2536G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444781 | |||||||
| chr3:133444793 | A | G | 1 | a0006c0009t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-2524A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444793 | |||||||
| chr3:133444823 | C | T | 2 | a0001c0002t0001g0092 a0001c0002t0001g0223 |
2 | NA18972.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.490-2494C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444823 | |||||||
| chr3:133444913 | C | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0027 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2404C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444913 | |||||||
| chr3:133444960 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0147 others(1): Show |
5 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2357A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133444960 | |||||||
| chr3:133445008 | G | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 |
3 | HG02109.hp1 HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.490-2309G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445008 | |||||||
| chr3:133445018 | A | G | 24 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0029 others(21): Show |
24 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-2299A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445018 | |||||||
| chr3:133445047 | G | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0027 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2270G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445047 | |||||||
| chr3:133445169 | T | A | 34 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(31): Show |
34 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.490-2148T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445169 | |||||||
| chr3:133445397 | G | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0029 others(21): Show |
24 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-1920G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445397 | |||||||
| chr3:133445884 | AG | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0027 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-1430delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133445884 | ||||||
| chr3:133445944 | C | G | 1 | a0001c0001t0001g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.490-1373C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445944 | |||||||
| chr3:133445994 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.490-1323G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133445994 | |||||||
| chr3:133446044 | A | G | 24 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0029 others(21): Show |
24 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-1273A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446044 | |||||||
| chr3:133446052 | C | T | 1 | a0001c0002t0001g0201 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.490-1265C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446052 | |||||||
| chr3:133446054 | C | G | 3 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0001g0258 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.490-1263C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446054 | |||||||
| chr3:133446106 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0137 |
2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490-1211A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446106 | |||||||
| chr3:133446335 | A | G | 1 | a0001c0004t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.490-982A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446335 | |||||||
| chr3:133446410 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-907G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446410 | |||||||
| chr3:133446570 | T | A | 1 | a0001c0002t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.490-747T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446570 | |||||||
| chr3:133446570 | T | TTA | 9 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0224 others(6): Show |
9 | HG01255.hp1 HG01515.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-678_490-677dup others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | T | TTATA | 4 | a0001c0001t0001g0161 a0001c0001t0001g0186 a0001c0001t0001g0235 others(1): Show |
4 | HG01192.hp2 HG02055.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-680_490-677dup others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0084 a0001c0001t0001g0182 a0001c0001t0001g0214 |
3 | HG03139.hp2 NA18948.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.490-684_490-677dup others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0254 |
2 | NA18956.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.490-686_490-677dup others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0062 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.490-690_490-677dup others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0114 a0001c0001t0001g0164 |
2 | HG02145.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.490-694_490-677dup others(18): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | T | TTTTA | 3 | a0001c0001t0001g0174 a0001c0002t0001g0081 a0002c0003t0001g0261 |
3 | HG01515.hp2 NA18955.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.490-746_490-745ins others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | T | TTTTATA | 3 | a0001c0002t0001g0111 a0001c0002t0001g0211 a0002c0003t0001g0003 |
4 | HG01069.hp2 HG01071.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-746_490-745ins others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | T | TTTTATAT others(3): Show |
1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-746_490-745ins others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | T | TTTTATAT others(5): Show |
1 | a0001c0001t0001g0108 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.490-746_490-745ins others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTA | T | 11 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0149 others(8): Show |
11 | HG01106.hp1 HG01516.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-678_490-677del others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATA | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0056 a0001c0001t0001g0097 others(13): Show |
16 | HG01070.hp2 HG01175.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-680_490-677del others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATA | T | 13 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0069 others(10): Show |
13 | HG00099.hp2 HG01123.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-682_490-677del others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(1): Show |
T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0044 others(19): Show |
22 | HG01257.hp2 HG01258.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.490-684_490-677del others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(3): Show |
T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0051 a0001c0001t0001g0074 others(12): Show |
15 | HG01106.hp2 HG01123.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.490-686_490-677del others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(5): Show |
T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0209 others(5): Show |
8 | HG03041.hp2 HG03704.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-688_490-677del others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(7): Show |
T | 21 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0046 others(18): Show |
21 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.490-690_490-677del others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(9): Show |
T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
18 | HG00423.hp1 HG00738.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-692_490-677del others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(11): Show |
T | 15 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0070 others(12): Show |
15 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.490-694_490-677del others(18): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(13): Show |
T | 11 | a0001c0001t0001g0094 a0001c0001t0001g0190 a0001c0002t0001g0037 others(8): Show |
11 | HG02083.hp1 HG02523.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-696_490-677del others(20): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(15): Show |
T | 13 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0002t0001g0055 others(10): Show |
13 | HG01891.hp1 HG02015.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-698_490-677del others(22): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(17): Show |
T | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.490-700_490-677del others(24): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(19): Show |
T | 1 | a0001c0001t0001g0079 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.490-702_490-677del others(26): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(21): Show |
T | 4 | a0001c0001t0001g0107 a0001c0001t0001g0147 a0001c0001t0001g0173 others(1): Show |
4 | HG01884.hp2 HG03017.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-704_490-677del others(28): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(23): Show |
T | 1 | a0001c0001t0001g0007 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.490-706_490-677del others(30): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(25): Show |
T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0023 |
3 | HG02257.hp2 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.490-708_490-677del others(32): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(27): Show |
T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0271 |
2 | HG00639.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.490-710_490-677del others(34): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(29): Show |
T | 1 | a0001c0002t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-712_490-677del others(36): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(31): Show |
T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0266 others(2): Show |
6 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-714_490-677del others(38): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(33): Show |
T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0002t0001g0068 others(3): Show |
8 | HG00735.hp2 HG01255.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-716_490-677del others(40): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(35): Show |
T | 6 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | HG01243.hp2 HG01257.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-718_490-677del others(42): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(37): Show |
T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0137 a0004c0006t0001g0172 |
3 | HG02257.hp1 HG04204.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.490-720_490-677del others(44): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(43): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.490-726_490-677del others(50): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446570 | TTATATAT others(51): Show |
T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0024 others(7): Show |
10 | HG01884.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-734_490-677del others(58): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446570 | ||||||
| chr3:133446571 | TATATATA others(4): Show |
T | 2 | a0001c0002t0001g0234 a0003c0010t0001g0156 |
2 | HG00558.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.490-745_490-735del others(11): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446571 | |||||||
| chr3:133446571 | TATATATA others(8): Show |
T | 1 | a0001c0002t0001g0049 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.490-745_490-731del others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446571 | |||||||
| chr3:133446571 | TATATATA others(10): Show |
T | 2 | a0001c0001t0001g0237 a0001c0002t0002g0225 |
2 | HG02004.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.490-745_490-729del others(17): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446571 | |||||||
| chr3:133446572 | A | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0144 a0001c0001t0001g0184 others(5): Show |
8 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-745A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446572 | |||||||
| chr3:133446574 | A | T | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0149 others(6): Show |
9 | HG01516.hp1 HG01517.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-743A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446574 | |||||||
| chr3:133446576 | A | T | 8 | a0001c0001t0001g0056 a0001c0001t0001g0148 a0001c0001t0001g0258 others(5): Show |
8 | HG01070.hp2 HG01928.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-741A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446576 | |||||||
| chr3:133446578 | A | T | 5 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0001c0001t0001g0181 others(2): Show |
5 | HG00099.hp2 HG02886.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-739A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446578 | |||||||
| chr3:133446579 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490-738T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446579 | |||||||
| chr3:133446580 | A | T | 16 | a0001c0001t0001g0014 a0001c0001t0001g0082 a0001c0001t0001g0085 others(13): Show |
16 | HG01952.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-737A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446580 | |||||||
| chr3:133446581 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-736T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446581 | |||||||
| chr3:133446582 | A | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0112 a0001c0001t0001g0113 others(6): Show |
9 | HG01106.hp2 HG01123.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-735A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446582 | |||||||
| chr3:133446583 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.490-734T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446583 | |||||||
| chr3:133446584 | A | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0209 others(5): Show |
8 | HG03041.hp2 HG03704.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-733A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446584 | |||||||
| chr3:133446586 | A | T | 19 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0046 others(16): Show |
19 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-731A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446586 | |||||||
| chr3:133446588 | A | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
14 | HG00423.hp1 HG00738.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-729A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446588 | |||||||
| chr3:133446590 | A | T | 13 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0075 others(10): Show |
13 | HG00639.hp1 HG01167.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-727A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446590 | |||||||
| chr3:133446592 | A | T | 11 | a0001c0001t0001g0094 a0001c0001t0001g0190 a0001c0002t0001g0037 others(8): Show |
11 | HG02083.hp1 HG02523.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-725A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446592 | |||||||
| chr3:133446594 | A | T | 8 | a0001c0001t0001g0020 a0001c0002t0001g0067 a0001c0002t0001g0096 others(5): Show |
8 | HG01891.hp1 HG02015.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-723A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446594 | |||||||
| chr3:133446596 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.490-721A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446596 | |||||||
| chr3:133446600 | A | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0173 |
2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.490-717A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446600 | |||||||
| chr3:133446606 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490-711A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446606 | |||||||
| chr3:133446608 | A | T | 1 | a0001c0002t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-709A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446608 | |||||||
| chr3:133446610 | A | T | 2 | a0001c0002t0001g0040 a0001c0002t0001g0078 |
2 | HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.490-707A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446610 | |||||||
| chr3:133446612 | A | T | 3 | a0001c0002t0001g0068 a0001c0002t0001g0087 a0001c0002t0001g0192 |
3 | HG00735.hp2 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.490-705A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446612 | |||||||
| chr3:133446614 | A | T | 1 | a0001c0002t0001g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.490-703A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446614 | |||||||
| chr3:133446616 | A | T | 1 | a0004c0006t0001g0172 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.490-701A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446616 | |||||||
| chr3:133446625 | TATATATA others(8): Show |
T | 1 | a0001c0002t0001g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490-690_490-676del others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 133446625 | ||||||
| chr3:133446639 | T | A | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.490-678T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446639 | |||||||
| chr3:133446641 | A | T | 1 | a0001c0002t0001g0229 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.490-676A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446641 | |||||||
| chr3:133446642 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490-675A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446642 | |||||||
| chr3:133446654 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | NA18956.hp2 NA18972.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.490-663G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133446654 | |||||||
| chr3:133447017 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0027 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-300A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 1/6 | chr3 | 133447017 | |||||||
| chr3:133447559 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.572+160A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133447559 | |||||||
| chr3:133447740 | T | G | 161 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(158): Show |
162 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.572+341T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133447740 | |||||||
| chr3:133447981 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0097 |
3 | HG01175.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.573-508G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133447981 | |||||||
| chr3:133448014 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0143 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.573-475G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133448014 | |||||||
| chr3:133448267 | T | C | 2 | a0001c0002t0001g0031 a0001c0002t0001g0169 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.573-222T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133448267 | |||||||
| chr3:133448272 | C | T | 3 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0116 |
3 | NA18960.hp2 NA18983.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.573-217C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133448272 | |||||||
| chr3:133448273 | G | A | 36 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(33): Show |
36 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.573-216G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 2/6 | chr3 | 133448273 | |||||||
| chr3:133448937 | C | T | 1 | a0002c0003t0001g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.729+292C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133448937 | |||||||
| chr3:133448962 | G | GT | 37 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(34): Show |
38 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.729+326dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133448962 | ||||||
| chr3:133449064 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0133 others(2): Show |
5 | HG01884.hp1 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.729+419G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449064 | |||||||
| chr3:133449171 | G | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0143 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+526G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449171 | |||||||
| chr3:133449384 | G | T | 160 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.729+739G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449384 | |||||||
| chr3:133449405 | C | CTTTGTT | 34 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(31): Show |
34 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.729+781_729+786dup others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449405 | ||||||
| chr3:133449468 | T | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0249 |
2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.729+823T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449468 | |||||||
| chr3:133449500 | T | TTTTG | 4 | a0001c0001t0001g0070 a0001c0001t0001g0135 a0001c0001t0001g0149 others(1): Show |
4 | HG00738.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-771_730-768dup others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449500 | ||||||
| chr3:133449500 | TTTTGTTT others(1): Show |
T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(218): Show |
225 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.730-775_730-768del others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449500 | ||||||
| chr3:133449725 | A | G | 77 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(74): Show |
78 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.730-578A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449725 | |||||||
| chr3:133449753 | C | T | 1 | a0001c0002t0001g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.730-550C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449753 | |||||||
| chr3:133449861 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0250 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.730-442C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449861 | |||||||
| chr3:133449880 | C | A | 1 | a0001c0002t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.730-423C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449880 | |||||||
| chr3:133449949 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0004t0001g0033 |
5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-354A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449949 | |||||||
| chr3:133449949 | AAGAGAG | A | 23 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0026 others(20): Show |
23 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.730-348_730-343del others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449949 | ||||||
| chr3:133449955 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0013 others(52): Show |
56 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.730-348G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449955 | |||||||
| chr3:133449955 | G | GAA | 3 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0004t0001g0033 |
5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-347_730-346ins others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449955 | ||||||
| chr3:133449961 | AAG | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0137 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.730-338_730-337del others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449961 | ||||||
| chr3:133449963 | G | GAAGGAA | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0043 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-339_730-338ins others(6): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449963 | ||||||
| chr3:133449963 | G | GAAGGAAA others(3): Show |
16 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0052 others(13): Show |
16 | HG00423.hp2 HG00621.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.730-339_730-338ins others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449963 | ||||||
| chr3:133449964 | A | AAG | 18 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(15): Show |
21 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.730-339_730-338ins others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449964 | |||||||
| chr3:133449964 | A | AAGGAAAG others(8): Show |
11 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(8): Show |
11 | HG01081.hp2 HG01516.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.730-339_730-338ins others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449964 | |||||||
| chr3:133449964 | A | AAGGAAAG others(12): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0069 a0002c0003t0001g0219 others(1): Show |
4 | HG00099.hp2 HG01175.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-339_730-338ins others(19): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449964 | |||||||
| chr3:133449968 | A | AG | 18 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0046 others(15): Show |
18 | HG00423.hp2 HG00621.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.730-334dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449968 | ||||||
| chr3:133449968 | A | G | 20 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0027 others(17): Show |
20 | HG00099.hp2 HG01081.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.730-335A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449968 | |||||||
| chr3:133449969 | G | GA | 5 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0071 others(2): Show |
5 | HG02630.hp1 HG02717.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.730-332dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449969 | ||||||
| chr3:133449972 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0015 others(14): Show |
18 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.730-331G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449972 | |||||||
| chr3:133449972 | G | T | 4 | a0001c0002t0001g0037 a0001c0002t0001g0087 a0001c0002t0001g0192 others(1): Show |
4 | HG00735.hp2 HG01891.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-331G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449972 | |||||||
| chr3:133449976 | A | AG | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0269 others(1): Show |
6 | HG01255.hp2 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.730-326dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449976 | ||||||
| chr3:133449976 | A | G | 38 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(35): Show |
38 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.730-327A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449976 | |||||||
| chr3:133449978 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0029 others(8): Show |
12 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.730-325A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449978 | |||||||
| chr3:133449978 | AAGGAAAG others(9): Show |
A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0143 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-323_730-308del others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449978 | ||||||
| chr3:133449980 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(31): Show |
35 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.730-323G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449980 | |||||||
| chr3:133449982 | A | AAAGG | 17 | a0001c0001t0001g0105 a0001c0001t0001g0174 a0001c0002t0001g0031 others(14): Show |
17 | HG00423.hp1 HG00621.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.730-287_730-284dup others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | A | AAAGGAAG others(1): Show |
47 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0144 others(44): Show |
47 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.730-291_730-284dup others(8): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | A | AAAGGAAG others(5): Show |
34 | a0001c0001t0001g0113 a0001c0001t0001g0152 a0001c0001t0001g0173 others(31): Show |
35 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.730-295_730-284dup others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | A | AAAGGAAG others(9): Show |
17 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0076 others(14): Show |
17 | HG00099.hp1 HG01243.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.730-299_730-284dup others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | A | AAAGGAAG others(13): Show |
6 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0075 others(3): Show |
6 | HG01081.hp1 HG01346.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-303_730-284dup others(20): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | A | AAAGGAAG others(17): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0147 others(3): Show |
7 | HG01884.hp2 HG02004.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.730-307_730-284dup others(24): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | A | AAAGGAAG others(25): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0222 |
2 | HG01928.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.730-315_730-284dup others(32): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | A | AAAGGAAG others(29): Show |
1 | a0005c0005t0001g0093 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.730-319_730-284dup others(36): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | A | AAAGGAAG others(33): Show |
1 | a0001c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.730-284_730-283ins others(40): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | A | AAGG | 42 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0018 others(39): Show |
44 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.730-320_730-319ins others(3): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | A | AGGAAGGA others(3): Show |
1 | a0001c0002t0001g0221 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.730-321_730-320ins others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449982 | |||||||
| chr3:133449982 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0015 others(13): Show |
17 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.730-321A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449982 | |||||||
| chr3:133449982 | AAAGGAAG others(5): Show |
A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0149 a0001c0001t0001g0181 others(2): Show |
5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-295_730-284del others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449982 | AAAGGAAG others(9): Show |
A | 5 | a0001c0002t0001g0059 a0001c0002t0001g0088 a0001c0002t0001g0089 others(2): Show |
5 | HG01070.hp2 HG01074.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-299_730-284del others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133449982 | ||||||
| chr3:133449986 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.730-317G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449986 | |||||||
| chr3:133449998 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0143 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-305G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133449998 | |||||||
| chr3:133450016 | A | AGGAAGGA others(17): Show |
1 | a0001c0001t0001g0182 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.730-284_730-283ins others(24): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133450016 | ||||||
| chr3:133450016 | A | AGGAAGGA others(9): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0161 a0001c0001t0001g0163 others(2): Show |
5 | HG01123.hp2 HG02055.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-284_730-283ins others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133450016 | ||||||
| chr3:133450016 | A | AGGAAGGA others(5): Show |
5 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0162 others(2): Show |
5 | HG02559.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-284_730-283ins others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133450016 | ||||||
| chr3:133450016 | A | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(75): Show |
79 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.730-287A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133450016 | |||||||
| chr3:133450056 | AAGAG | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0001g0149 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.730-241_730-238del others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 133450056 | ||||||
| chr3:133450237 | T | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0020 |
2 | HG02109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.730-66T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133450237 | |||||||
| chr3:133450283 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.730-20A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133450283 | |||||||
| chr3:133450296 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | NA18956.hp2 NA18972.hp2 NA19085.hp1 |
splice_region_variant&intron_variant | LOW | c.730-7T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 3/6 | chr3 | 133450296 | |||||||
| chr3:133450477 | A | G | 1 | a0004c0006t0001g0172 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.891+13A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133450477 | |||||||
| chr3:133450781 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.891+317C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133450781 | |||||||
| chr3:133450843 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0246 |
2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.891+379A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133450843 | |||||||
| chr3:133450883 | G | A | 95 | a0001c0002t0001g0016 a0001c0002t0001g0035 a0001c0002t0001g0037 others(92): Show |
95 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.891+419G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133450883 | |||||||
| chr3:133450988 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0004t0001g0033 |
5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+524G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133450988 | |||||||
| chr3:133451110 | C | CA | 188 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.891+665dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133451110 | ||||||
| chr3:133451110 | C | CAA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(38): Show |
43 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.891+664_891+665dup others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133451110 | ||||||
| chr3:133451110 | CA | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0001g0149 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+665delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133451110 | ||||||
| chr3:133451185 | A | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0133 others(2): Show |
5 | HG01884.hp1 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+721A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451185 | |||||||
| chr3:133451223 | A | G | 1 | a0001c0002t0001g0185 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.891+759A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451223 | |||||||
| chr3:133451254 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.891+790A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451254 | |||||||
| chr3:133451276 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.891+812T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451276 | |||||||
| chr3:133451313 | CATA | C | 16 | a0001c0001t0001g0062 a0001c0001t0001g0072 a0001c0001t0001g0073 others(13): Show |
16 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.891+853_891+855del others(3): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133451313 | ||||||
| chr3:133451321 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
237 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.891+857G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451321 | |||||||
| chr3:133451377 | A | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(95): Show |
100 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.891+913A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451377 | |||||||
| chr3:133451386 | G | A | 1 | a0002c0003t0001g0219 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.891+922G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451386 | |||||||
| chr3:133451514 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0032 others(6): Show |
9 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.891+1050C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451514 | |||||||
| chr3:133451592 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.891+1128T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451592 | |||||||
| chr3:133451845 | T | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0210 a0001c0001t0001g0231 |
3 | HG01952.hp1 HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.891+1381T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451845 | |||||||
| chr3:133451893 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.891+1429A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133451893 | |||||||
| chr3:133452315 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0147 others(2): Show |
6 | HG01123.hp2 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+1851C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452315 | |||||||
| chr3:133452440 | C | A | 96 | a0001c0001t0001g0094 a0001c0002t0001g0016 a0001c0002t0001g0035 others(93): Show |
96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.891+1976C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452440 | |||||||
| chr3:133452458 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0001g0258 |
3 | HG01891.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.891+1994C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452458 | |||||||
| chr3:133452515 | T | G | 106 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(103): Show |
107 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.891+2051T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452515 | |||||||
| chr3:133452583 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.891+2119A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452583 | |||||||
| chr3:133452661 | C | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
74 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.891+2197C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452661 | |||||||
| chr3:133452898 | A | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
109 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.891+2434A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133452898 | |||||||
| chr3:133453079 | G | T | 35 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(32): Show |
35 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.891+2615G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453079 | |||||||
| chr3:133453347 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.891+2883C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453347 | |||||||
| chr3:133453350 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.891+2886T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453350 | |||||||
| chr3:133453517 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.891+3053C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453517 | |||||||
| chr3:133453530 | C | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
109 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.891+3066C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453530 | |||||||
| chr3:133453602 | A | G | 100 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
101 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.891+3138A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453602 | |||||||
| chr3:133453788 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0246 |
3 | HG02451.hp2 HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.891+3324C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453788 | |||||||
| chr3:133453861 | T | A | 21 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0062 others(18): Show |
21 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.891+3397T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453861 | |||||||
| chr3:133453869 | T | A | 1 | a0006c0009t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.891+3405T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453869 | |||||||
| chr3:133453906 | C | T | 19 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0074 others(16): Show |
19 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.891+3442C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453906 | |||||||
| chr3:133453923 | T | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0022 others(116): Show |
120 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.891+3459T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453923 | |||||||
| chr3:133453965 | G | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0022 others(19): Show |
23 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.891+3501G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133453965 | |||||||
| chr3:133454213 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0155 |
3 | HG01243.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.891+3749A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454213 | |||||||
| chr3:133454352 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.891+3888T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454352 | |||||||
| chr3:133454359 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0162 a0001c0001t0001g0166 |
3 | HG02559.hp2 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.891+3895T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454359 | |||||||
| chr3:133454506 | A | G | 36 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(33): Show |
36 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.891+4042A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454506 | |||||||
| chr3:133454520 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.891+4056G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454520 | |||||||
| chr3:133454559 | C | G | 1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.891+4095C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454559 | |||||||
| chr3:133454749 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0112 others(1): Show |
4 | HG02630.hp2 HG02818.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+4285C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454749 | |||||||
| chr3:133454813 | T | A | 1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.891+4349T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454813 | |||||||
| chr3:133454831 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0162 others(5): Show |
8 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.891+4367A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454831 | |||||||
| chr3:133454885 | G | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.891+4421G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133454885 | |||||||
| chr3:133455148 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.891+4684T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455148 | |||||||
| chr3:133455208 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.891+4744A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455208 | |||||||
| chr3:133455223 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.891+4759C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455223 | |||||||
| chr3:133455309 | G | T | 1 | a0001c0002t0001g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.891+4845G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455309 | |||||||
| chr3:133455335 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(98): Show |
103 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.891+4871C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455335 | |||||||
| chr3:133455605 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(63): Show |
68 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.891+5141C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455605 | |||||||
| chr3:133455654 | T | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0022 others(116): Show |
120 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.891+5190T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455654 | |||||||
| chr3:133455705 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+5241A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455705 | |||||||
| chr3:133455806 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0165 a0001c0004t0001g0034 |
3 | HG01123.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.891+5342G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455806 | |||||||
| chr3:133455991 | C | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0161 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.891+5527C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133455991 | |||||||
| chr3:133456405 | T | A | 1 | a0001c0002t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.891+5941T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456405 | |||||||
| chr3:133456425 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(223): Show |
231 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.891+5961T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456425 | |||||||
| chr3:133456437 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.891+5973G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456437 | |||||||
| chr3:133456459 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(33): Show |
38 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.891+5995G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456459 | |||||||
| chr3:133456473 | G | C | 1 | a0001c0002t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.891+6009G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456473 | |||||||
| chr3:133456527 | G | A | 2 | a0001c0002t0001g0055 a0001c0002t0001g0098 |
2 | NA18973.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.891+6063G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456527 | |||||||
| chr3:133456548 | A | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+6084A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456548 | |||||||
| chr3:133456576 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.891+6112G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456576 | |||||||
| chr3:133456616 | T | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0074 others(13): Show |
16 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+6152T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456616 | |||||||
| chr3:133456801 | A | T | 1 | a0001c0001t0001g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.891+6337A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456801 | |||||||
| chr3:133456918 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0193 |
2 | HG02129.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.891+6454A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456918 | |||||||
| chr3:133456940 | T | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0020 |
2 | HG02109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.891+6476T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133456940 | |||||||
| chr3:133456994 | C | CT | 16 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0074 others(13): Show |
16 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.891+6534dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133456994 | ||||||
| chr3:133457118 | G | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0160 |
2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.891+6654G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457118 | |||||||
| chr3:133457493 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0250 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.891+7029A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457493 | |||||||
| chr3:133457556 | A | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0147 others(2): Show |
6 | HG01123.hp2 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+7092A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457556 | |||||||
| chr3:133457558 | T | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
60 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.891+7094T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457558 | |||||||
| chr3:133457631 | G | C | 1 | a0001c0002t0001g0199 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.891+7167G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457631 | |||||||
| chr3:133457688 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0161 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.891+7224A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457688 | |||||||
| chr3:133457728 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.891+7264T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457728 | |||||||
| chr3:133457729 | C | T | 1 | a0002c0003t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.891+7265C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457729 | |||||||
| chr3:133457911 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.891+7447T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457911 | |||||||
| chr3:133457953 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0162 others(5): Show |
8 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.891+7489A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133457953 | |||||||
| chr3:133458004 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0147 others(2): Show |
6 | HG01123.hp2 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+7540A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458004 | |||||||
| chr3:133458326 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.891+7862T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458326 | |||||||
| chr3:133458492 | A | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(33): Show |
38 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.891+8028A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458492 | |||||||
| chr3:133458504 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0004t0001g0033 |
5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+8040G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458504 | |||||||
| chr3:133458519 | C | T | 35 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(32): Show |
35 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.891+8055C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458519 | |||||||
| chr3:133458662 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.892-8166C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458662 | |||||||
| chr3:133458724 | C | G | 2 | a0001c0002t0001g0028 a0001c0002t0001g0054 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.892-8104C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458724 | |||||||
| chr3:133458840 | C | T | 1 | a0002c0007t0001g0243 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.892-7988C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458840 | |||||||
| chr3:133458918 | G | A | 37 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(34): Show |
37 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.892-7910G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458918 | |||||||
| chr3:133458922 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0162 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.892-7906G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458922 | |||||||
| chr3:133458969 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0162 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.892-7859C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458969 | |||||||
| chr3:133458988 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.892-7840G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133458988 | |||||||
| chr3:133459011 | C | T | 59 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(56): Show |
59 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.892-7817C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459011 | |||||||
| chr3:133459104 | C | T | 37 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(34): Show |
37 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.892-7724C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459104 | |||||||
| chr3:133459304 | G | A | 119 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0025 others(116): Show |
120 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.892-7524G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459304 | |||||||
| chr3:133459427 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0155 |
3 | HG01243.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.892-7401T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459427 | |||||||
| chr3:133459588 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(234): Show |
241 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.892-7240C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459588 | |||||||
| chr3:133459656 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0129 others(1): Show |
6 | HG01255.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-7172C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459656 | |||||||
| chr3:133459678 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892-7150T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459678 | |||||||
| chr3:133459723 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.892-7105C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133459723 | |||||||
| chr3:133460360 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0230 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.892-6468C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133460360 | |||||||
| chr3:133460586 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0258 |
2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.892-6242C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133460586 | |||||||
| chr3:133460675 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0147 |
3 | HG01884.hp2 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.892-6153C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133460675 | |||||||
| chr3:133460736 | C | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0036 others(93): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.892-6092C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133460736 | |||||||
| chr3:133460760 | A | G | 1 | a0001c0002t0001g0035 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.892-6068A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133460760 | |||||||
| chr3:133461089 | G | A | 29 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(26): Show |
29 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.892-5739G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461089 | |||||||
| chr3:133461113 | C | A | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.892-5715C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461113 | |||||||
| chr3:133461329 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.892-5499G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461329 | |||||||
| chr3:133461413 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
73 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.892-5415C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461413 | |||||||
| chr3:133461605 | A | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
73 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.892-5223A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461605 | |||||||
| chr3:133461631 | A | G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0146 others(5): Show |
8 | HG02145.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-5197A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461631 | |||||||
| chr3:133461657 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0212 |
2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.892-5171T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133461657 | |||||||
| chr3:133462036 | G | A | 49 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(46): Show |
49 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.892-4792G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462036 | |||||||
| chr3:133462071 | TG | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.892-4755delG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133462071 | ||||||
| chr3:133462073 | G | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.892-4755G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462073 | |||||||
| chr3:133462153 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0143 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.892-4675G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462153 | |||||||
| chr3:133462161 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0155 |
3 | HG01243.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.892-4667G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462161 | |||||||
| chr3:133462226 | C | T | 44 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(41): Show |
45 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.892-4602C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462226 | |||||||
| chr3:133462247 | T | TA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(100): Show |
106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.892-4574dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133462247 | ||||||
| chr3:133462251 | A | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
73 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.892-4577A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462251 | |||||||
| chr3:133462302 | T | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0152 a0001c0001t0001g0230 others(10): Show |
14 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.892-4526T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462302 | |||||||
| chr3:133462420 | G | T | 1 | a0001c0002t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.892-4408G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462420 | |||||||
| chr3:133462492 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0112 a0001c0001t0001g0267 |
3 | HG02630.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.892-4336G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462492 | |||||||
| chr3:133462544 | C | T | 4 | a0001c0002t0001g0040 a0001c0002t0001g0087 a0001c0002t0001g0227 others(1): Show |
4 | HG00099.hp1 HG01106.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-4284C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462544 | |||||||
| chr3:133462767 | T | A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(41): Show |
45 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.892-4061T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462767 | |||||||
| chr3:133462981 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0027 |
2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.892-3847A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133462981 | |||||||
| chr3:133463034 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.892-3794T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463034 | |||||||
| chr3:133463081 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892-3747G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463081 | |||||||
| chr3:133463092 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(100): Show |
106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.892-3736T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463092 | |||||||
| chr3:133463106 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.892-3722C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463106 | |||||||
| chr3:133463243 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.892-3585A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463243 | |||||||
| chr3:133463300 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(66): Show |
70 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.892-3528A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463300 | |||||||
| chr3:133463460 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.892-3368C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463460 | |||||||
| chr3:133463573 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
262 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(259): Show |
intron_variant | MODIFIER | c.892-3255A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463573 | |||||||
| chr3:133463855 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0155 |
3 | HG01243.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.892-2973C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463855 | |||||||
| chr3:133463869 | C | G | 1 | a0001c0002t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.892-2959C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463869 | |||||||
| chr3:133463913 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.892-2915C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133463913 | |||||||
| chr3:133464031 | C | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(15): Show |
19 | HG01123.hp2 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.892-2797C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464031 | |||||||
| chr3:133464080 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.892-2748G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464080 | |||||||
| chr3:133464623 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(100): Show |
106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.892-2205T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464623 | |||||||
| chr3:133464661 | T | TAC | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.892-2166_892-2165i others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133464661 | ||||||
| chr3:133464663 | G | T | 1 | a0002c0007t0001g0243 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.892-2165G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464663 | |||||||
| chr3:133464705 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.892-2123G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464705 | |||||||
| chr3:133464908 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.892-1920G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133464908 | |||||||
| chr3:133465001 | C | CT | 6 | a0001c0001t0001g0184 a0001c0001t0001g0235 a0001c0002t0001g0031 others(3): Show |
6 | HG02071.hp2 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.892-1809dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133465001 | ||||||
| chr3:133465001 | CT | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0152 others(14): Show |
18 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-1809delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133465001 | ||||||
| chr3:133465163 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.892-1665C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465163 | |||||||
| chr3:133465427 | T | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0146 others(5): Show |
8 | HG02145.hp1 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-1401T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465427 | |||||||
| chr3:133465476 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0231 |
2 | HG01952.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.892-1352G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465476 | |||||||
| chr3:133465540 | T | G | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.892-1288T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465540 | |||||||
| chr3:133465708 | G | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.892-1120G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465708 | |||||||
| chr3:133465867 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.892-961C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465867 | |||||||
| chr3:133465887 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0138 |
3 | HG02109.hp1 HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.892-941T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133465887 | |||||||
| chr3:133466009 | A | G | 1 | a0001c0002t0001g0206 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.892-819A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466009 | |||||||
| chr3:133466047 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0143 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.892-781G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466047 | |||||||
| chr3:133466088 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(100): Show |
106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.892-740G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466088 | |||||||
| chr3:133466158 | AC | A | 7 | a0001c0001t0001g0079 a0001c0001t0001g0123 a0001c0001t0001g0127 others(4): Show |
7 | HG02015.hp1 HG02071.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.892-668delC | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466158 | ||||||
| chr3:133466167 | C | CG | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(146): Show |
152 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.892-653dupG | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466167 | ||||||
| chr3:133466406 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0143 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.892-422G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466406 | |||||||
| chr3:133466429 | T | C | 1 | a0001c0002t0001g0199 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.892-399T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466429 | |||||||
| chr3:133466450 | C | T | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
97 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.892-378C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466450 | |||||||
| chr3:133466661 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.892-167C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466661 | |||||||
| chr3:133466677 | C | CAAAAAAA others(2): Show |
41 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(38): Show |
43 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.892-139_892-131dup others(9): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | ||||||
| chr3:133466677 | C | CAAAAAAA others(3): Show |
53 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0025 others(50): Show |
53 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.892-140_892-131dup others(10): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | ||||||
| chr3:133466677 | C | CAAAAAAA others(4): Show |
22 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0029 others(19): Show |
22 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.892-141_892-131dup others(11): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | ||||||
| chr3:133466677 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0010 |
2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.892-142_892-131dup others(12): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | ||||||
| chr3:133466677 | C | CAAAAAAA others(7): Show |
47 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0036 others(44): Show |
48 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.892-144_892-131dup others(14): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | ||||||
| chr3:133466677 | C | CAAAAAAA others(8): Show |
35 | a0001c0001t0001g0076 a0001c0001t0001g0094 a0001c0001t0001g0104 others(32): Show |
35 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.892-145_892-131dup others(15): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | ||||||
| chr3:133466677 | C | CAAAAAAA others(9): Show |
10 | a0001c0001t0001g0017 a0001c0001t0001g0266 a0001c0002t0001g0049 others(7): Show |
10 | HG01169.hp2 HG01952.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.892-146_892-131dup others(16): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | ||||||
| chr3:133466677 | C | CAAAAAAA others(10): Show |
9 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0066 others(6): Show |
9 | HG00738.hp1 HG01243.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.892-147_892-131dup others(17): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | ||||||
| chr3:133466677 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.892-148_892-131dup others(18): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 133466677 | ||||||
| chr3:133466701 | G | A | 2 | a0001c0002t0001g0191 a0001c0002t0001g0220 |
2 | HG00735.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.892-127G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466701 | |||||||
| chr3:133466811 | G | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0158 |
2 | HG00738.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.892-17G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466811 | |||||||
| chr3:133466814 | C | T | 1 | a0001c0002t0001g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.892-14C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 4/6 | chr3 | 133466814 | |||||||
| chr3:133466990 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(127): Show |
134 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1023+31T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133466990 | |||||||
| chr3:133467004 | ACT | A | 49 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(46): Show |
49 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1023+50_1023+51del others(2): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 133467004 | ||||||
| chr3:133467158 | C | T | 36 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(33): Show |
36 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1023+199C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467158 | |||||||
| chr3:133467215 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1023+256G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467215 | |||||||
| chr3:133467304 | G | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.1023+345G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467304 | |||||||
| chr3:133467322 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0004t0001g0033 |
5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+363G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467322 | |||||||
| chr3:133467375 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0004t0001g0033 |
5 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+416T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467375 | |||||||
| chr3:133467420 | C | T | 1 | a0001c0002t0001g0218 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1023+461C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467420 | |||||||
| chr3:133467569 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1023+610T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467569 | |||||||
| chr3:133467664 | C | T | 8 | a0001c0002t0001g0035 a0001c0002t0001g0048 a0001c0002t0001g0049 others(5): Show |
8 | HG00558.hp1 HG00597.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+705C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467664 | |||||||
| chr3:133467841 | C | T | 1 | a0001c0002t0001g0040 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1023+882C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467841 | |||||||
| chr3:133467897 | G | T | 94 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(91): Show |
95 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.1023+938G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467897 | |||||||
| chr3:133467984 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1023+1025A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133467984 | |||||||
| chr3:133468058 | G | A | 2 | a0001c0001t0001g0182 a0001c0004t0001g0034 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1023+1099G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468058 | |||||||
| chr3:133468096 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1023+1137A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468096 | |||||||
| chr3:133468128 | T | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(28): Show |
32 | HG01123.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1023+1169T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468128 | |||||||
| chr3:133468155 | C | A | 1 | a0006c0009t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1023+1196C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468155 | |||||||
| chr3:133468169 | TCCCTGCC others(19): Show |
T | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1023+1211_1023+123 others(30): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468169 | |||||||
| chr3:133468172 | C | G | 1 | a0001c0002t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1023+1213C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468172 | |||||||
| chr3:133468293 | C | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(27): Show |
31 | HG01123.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1023+1334C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468293 | |||||||
| chr3:133468321 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1023+1362G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468321 | |||||||
| chr3:133468469 | T | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(28): Show |
32 | HG01123.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1023+1510T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468469 | |||||||
| chr3:133468572 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1023+1613G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468572 | |||||||
| chr3:133468596 | T | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(15): Show |
19 | HG01123.hp2 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1023+1637T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468596 | |||||||
| chr3:133468616 | G | A | 1 | a0001c0002t0001g0229 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1023+1657G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468616 | |||||||
| chr3:133468735 | A | G | 1 | a0001c0002t0001g0203 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1023+1776A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133468735 | |||||||
| chr3:133469035 | G | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0146 others(6): Show |
9 | HG02145.hp1 HG02559.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1023+2076G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469035 | |||||||
| chr3:133469203 | A | G | 1 | a0001c0002t0001g0234 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1023+2244A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469203 | |||||||
| chr3:133469220 | G | A | 1 | a0001c0002t0001g0252 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1023+2261G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469220 | |||||||
| chr3:133469224 | C | A | 1 | a0001c0001t0001g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1023+2265C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469224 | |||||||
| chr3:133469440 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1023+2481T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469440 | |||||||
| chr3:133469541 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0212 |
2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1023+2582T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469541 | |||||||
| chr3:133469936 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0136 others(6): Show |
10 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1024-2409C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133469936 | |||||||
| chr3:133470018 | CT | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(96): Show |
102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1024-2324delT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 133470018 | ||||||
| chr3:133470188 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(96): Show |
102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1024-2157G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470188 | |||||||
| chr3:133470193 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0130 others(5): Show |
8 | HG01123.hp2 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1024-2152G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470193 | |||||||
| chr3:133470348 | T | C | 110 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
111 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.1024-1997T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470348 | |||||||
| chr3:133470472 | A | G | 72 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
72 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1024-1873A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470472 | |||||||
| chr3:133470558 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0143 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1024-1787G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470558 | |||||||
| chr3:133470596 | G | C | 1 | a0001c0001t0001g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1024-1749G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470596 | |||||||
| chr3:133470692 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1024-1653A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470692 | |||||||
| chr3:133470871 | A | C | 2 | a0001c0001t0001g0118 a0001c0002t0001g0126 |
2 | HG02071.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1024-1474A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470871 | |||||||
| chr3:133470887 | C | T | 1 | a0001c0002t0001g0208 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1024-1458C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470887 | |||||||
| chr3:133470888 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0155 |
3 | HG01243.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1024-1457G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470888 | |||||||
| chr3:133470905 | G | C | 1 | a0001c0002t0001g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1024-1440G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470905 | |||||||
| chr3:133470919 | G | A | 2 | a0001c0001t0001g0005 a0001c0002t0001g0270 |
2 | HG01891.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1024-1426G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133470919 | |||||||
| chr3:133471285 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1024-1060G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471285 | |||||||
| chr3:133471346 | C | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0017 others(96): Show |
102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1024-999C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471346 | |||||||
| chr3:133471487 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0130 others(5): Show |
8 | HG01123.hp2 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1024-858C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471487 | |||||||
| chr3:133471520 | T | C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0112 a0001c0001t0001g0144 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1024-825T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471520 | |||||||
| chr3:133471747 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1024-598G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471747 | |||||||
| chr3:133471921 | G | T | 1 | a0001c0001t0001g0043 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1024-424G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133471921 | |||||||
| chr3:133472033 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1024-312C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133472033 | |||||||
| chr3:133472102 | C | T | 1 | a0001c0002t0001g0226 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1024-243C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133472102 | |||||||
| chr3:133472249 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(131): Show |
138 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.1024-96A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 5/6 | chr3 | 133472249 | |||||||
| chr3:133472609 | A | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(152): Show |
156 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1244+44A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472609 | |||||||
| chr3:133472639 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1244+74C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472639 | |||||||
| chr3:133472663 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0129 others(1): Show |
6 | HG01255.hp2 HG02976.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1244+98C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472663 | |||||||
| chr3:133472743 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0182 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1244+178A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472743 | |||||||
| chr3:133472772 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1244+207T>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472772 | |||||||
| chr3:133472829 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0144 a0001c0001t0001g0258 |
3 | HG01175.hp1 HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1244+264G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472829 | |||||||
| chr3:133472932 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0144 a0001c0001t0001g0258 |
3 | HG01175.hp1 HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1244+367C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472932 | |||||||
| chr3:133472951 | C | CT | 7 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0030 others(4): Show |
7 | HG00738.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1244+400dupT | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 133472951 | ||||||
| chr3:133472991 | T | C | 1 | a0001c0002t0001g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1244+426T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133472991 | |||||||
| chr3:133473153 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0027 |
2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1244+588T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473153 | |||||||
| chr3:133473232 | C | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0136 others(7): Show |
11 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1244+667C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473232 | |||||||
| chr3:133473255 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0250 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1244+690C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473255 | |||||||
| chr3:133473325 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
204 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.1244+760C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473325 | |||||||
| chr3:133473438 | C | CA | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
147 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1244+894dupA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 133473438 | ||||||
| chr3:133473438 | C | CAA | 25 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0053 others(22): Show |
25 | HG00621.hp2 HG00738.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.1244+893_1244+894d others(4): Show |
BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 133473438 | ||||||
| chr3:133473438 | CA | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
22 | HG01123.hp2 HG01175.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1244+894delA | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 133473438 | ||||||
| chr3:133473482 | A | T | 9 | a0001c0001t0001g0069 a0002c0003t0001g0003 a0002c0003t0001g0115 others(6): Show |
10 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1244+917A>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473482 | |||||||
| chr3:133473579 | G | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0155 a0001c0002t0001g0031 others(1): Show |
4 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1244+1014G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473579 | |||||||
| chr3:133473633 | A | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0136 a0001c0001t0001g0140 others(4): Show |
8 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1244+1068A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473633 | |||||||
| chr3:133473675 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1244+1110G>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473675 | |||||||
| chr3:133473710 | A | G | 1 | a0006c0009t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1244+1145A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473710 | |||||||
| chr3:133473745 | G | A | 2 | a0001c0002t0001g0067 a0001c0002t0001g0087 |
2 | HG03942.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1244+1180G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473745 | |||||||
| chr3:133473773 | G | A | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1196G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473773 | |||||||
| chr3:133473774 | G | C | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1195G>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473774 | |||||||
| chr3:133473775 | G | A | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1194G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473775 | |||||||
| chr3:133473776 | T | C | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1193T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473776 | |||||||
| chr3:133473778 | A | C | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1191A>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473778 | |||||||
| chr3:133473781 | T | A | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1188T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473781 | |||||||
| chr3:133473782 | C | G | 1 | a0002c0003t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1245-1187C>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473782 | |||||||
| chr3:133473787 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0041 others(98): Show |
102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1245-1182G>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133473787 | |||||||
| chr3:133474222 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0030 others(4): Show |
7 | HG01891.hp1 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1245-747T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474222 | |||||||
| chr3:133474332 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1245-637C>T | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474332 | |||||||
| chr3:133474398 | T | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0250 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1245-571T>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474398 | |||||||
| chr3:133474468 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0030 others(4): Show |
7 | HG01891.hp1 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1245-501A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474468 | |||||||
| chr3:133474556 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0250 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1245-413T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474556 | |||||||
| chr3:133474568 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(145): Show |
151 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1245-401A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474568 | |||||||
| chr3:133474646 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1245-323T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474646 | |||||||
| chr3:133474690 | C | A | 1 | a0001c0002t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1245-279C>A | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474690 | |||||||
| chr3:133474693 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0155 a0001c0002t0001g0031 others(1): Show |
4 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1245-276A>G | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474693 | |||||||
| chr3:133474713 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0020 others(6): Show |
9 | HG01891.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1245-256T>C | BFSP2 | ENSG00000170819.5 | transcript | ENST00000302334.3 | protein_coding | 6/6 | chr3 | 133474713 |