Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10818 |
|---|---|
| ensemblid | ENSG00000166225.9 |
| hgncid | 16971 |
| symbol | FRS2 |
| name | fibroblast growth factor receptor substrate 2 |
| refseq_nuc | NM_001278356.2 |
| refseq_prot | NP_001265285.1 |
| ensembl_nuc | ENST00000549921.6 |
| ensembl_prot | ENSP00000450048.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 69470388 |
| end | 69579793 |
| strand | + |
| ver | v1.2 |
| region | chr12:69470388-69579793 |
| region5000 | chr12:69465388-69584793 |
| regionname0 | FRS2_chr12_69470388_69579793 |
| regionname5000 | FRS2_chr12_69465388_69584793 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 508 | 340 | 91 | 54 | 155 | 12 | 26 | 115 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0002 | 0/0 | 508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0003 | 0/0 | 100 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1527 | 221 | 56 | 27 | 115 | 7 | 14 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| c0002 | 0/0 | 1527 | 119 | 35 | 27 | 40 | 5 | 12 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| c0003 | 0/0 | 1499 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| c0004 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5241 | 85 | 25 | 11 | 37 | 3 | 9 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0002 | 0/0 | 5242 | 73 | 5 | 3 | 63 | 0 | 2 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0003 | 0/0 | 5242 | 66 | 11 | 15 | 30 | 1 | 9 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0004 | 1/0 | 5242 | 24 | 0 | 4 | 15 | 3 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0005 | 0/0 | 5243 | 13 | 12 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0006 | 0/0 | 5242 | 13 | 0 | 8 | 0 | 2 | 3 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0007 | 0/0 | 5241 | 8 | 7 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0008 | 0/0 | 5242 | 6 | 6 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0009 | 0/0 | 5241 | 6 | 6 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0010 | 0/0 | 5242 | 4 | 2 | 1 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0011 | 0/0 | 5241 | 4 | 4 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0012 | 0/0 | 5241 | 3 | 1 | 2 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0013 | 0/0 | 5241 | 3 | 0 | 0 | 3 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0014 | 0/0 | 5242 | 3 | 2 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0015 | 0/1 | 5242 | 3 | 1 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0016 | 0/0 | 5242 | 3 | 0 | 0 | 3 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0017 | 0/0 | 5242 | 2 | 2 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0018 | 0/0 | 5241 | 2 | 0 | 1 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0019 | 0/0 | 5241 | 2 | 0 | 2 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0020 | 0/0 | 5242 | 2 | 2 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0021 | 0/0 | 5241 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0022 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0023 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0024 | 0/0 | 5241 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0025 | 0/0 | 5243 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0026 | 0/0 | 5242 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0027 | 0/0 | 5242 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0028 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0029 | 0/0 | 5243 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0030 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0031 | 0/0 | 5243 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0032 | 0/0 | 5242 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0033 | 0/0 | 5243 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0034 | 0/0 | 5242 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0035 | 0/0 | 5242 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0036 | 0/0 | 5242 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| t0037 | 0/0 | 5241 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1527 | 221 | 56 | 27 | 115 | 7 | 14 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002 | 0/0 | 1527 | 119 | 35 | 27 | 40 | 5 | 12 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0002c0004 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0003c0003 | 0/0 | 1499 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6767 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0002 | 0/0 | 6768 | 72 | 5 | 3 | 62 | 0 | 2 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0003 | 0/0 | 6768 | 66 | 11 | 15 | 30 | 1 | 9 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0004 | 1/0 | 6768 | 24 | 0 | 4 | 15 | 3 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0005 | 0/0 | 6769 | 13 | 12 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0008 | 0/0 | 6768 | 6 | 6 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0009 | 0/0 | 6767 | 6 | 6 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0010 | 0/0 | 6768 | 4 | 2 | 1 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0013 | 0/0 | 6767 | 3 | 0 | 0 | 3 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0014 | 0/0 | 6768 | 3 | 2 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0015 | 0/1 | 6768 | 3 | 1 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0016 | 0/0 | 6768 | 3 | 0 | 0 | 3 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0017 | 0/0 | 6768 | 2 | 2 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0020 | 0/0 | 6768 | 2 | 2 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0022 | 0/0 | 6768 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0023 | 0/0 | 6768 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0025 | 0/0 | 6769 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0026 | 0/0 | 6768 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0027 | 0/0 | 6768 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0028 | 0/0 | 6768 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0029 | 0/0 | 6769 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0030 | 0/0 | 6768 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0031 | 0/0 | 6769 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0033 | 0/0 | 6769 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0034 | 0/0 | 6768 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0035 | 0/0 | 6768 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0001t0036 | 0/0 | 6768 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0001 | 0/0 | 6767 | 84 | 24 | 11 | 37 | 3 | 9 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0006 | 0/0 | 6768 | 13 | 0 | 8 | 0 | 2 | 3 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0007 | 0/0 | 6767 | 8 | 7 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0011 | 0/0 | 6767 | 3 | 3 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0012 | 0/0 | 6767 | 3 | 1 | 2 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0018 | 0/0 | 6767 | 2 | 0 | 1 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0019 | 0/0 | 6767 | 2 | 0 | 2 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0021 | 0/0 | 6767 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0024 | 0/0 | 6767 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0032 | 0/0 | 6768 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0001c0002t0037 | 0/0 | 6767 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0002c0004t0011 | 0/0 | 6767 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| a0003c0003t0002 | 0/0 | 6740 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | copy fasta | chr12 | 69465388 | 69584793 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0008g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0009g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0009g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0009g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0009g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0009g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0010g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0010g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0010g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0010g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0013g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0013g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0013g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0014g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0014g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0015g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0015g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0016g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0016g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0016g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0017g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0017g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0020g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0020g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0022g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0023g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0025g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0026g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0027g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0028g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0029g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0030g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0031g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0033g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0034g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0035g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0036g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0006g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0007g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0012g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0012g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0012g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0018g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0018g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0019g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0019g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0021g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0024g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0032g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0037g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0002c0004t0011g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0003c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0088 | EUR | GBR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0146 | EUR | GBR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00140 | hp1 | a0001 | c0001 | t0036 | g0046 | EUR | GBR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00140 | hp2 | a0001 | c0001 | t0010 | g0092 | EUR | GBR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00408 | hp1 | a0001 | c0002 | t0018 | g0116 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00639 | hp1 | a0001 | c0002 | t0006 | g0255 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00642 | hp2 | a0001 | c0002 | t0006 | g0252 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00733 | hp2 | a0001 | c0002 | t0019 | g0143 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00741 | hp1 | a0001 | c0002 | t0006 | g0253 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00741 | hp2 | a0001 | c0002 | t0007 | g0121 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01069 | hp1 | a0001 | c0001 | t0029 | g0206 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01069 | hp2 | a0001 | c0002 | t0006 | g0259 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01070 | hp2 | a0001 | c0002 | t0019 | g0142 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01071 | hp1 | a0001 | c0002 | t0006 | g0260 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01106 | hp2 | a0001 | c0002 | t0006 | g0261 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01109 | hp1 | a0001 | c0002 | t0006 | g0264 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0250 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01167 | hp2 | a0001 | c0001 | t0014 | g0009 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0093 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01192 | hp1 | a0001 | c0002 | t0012 | g0083 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01256 | hp1 | a0001 | c0002 | t0032 | g0254 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01361 | hp2 | a0001 | c0001 | t0025 | g0013 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0265 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0090 | EUR | IBS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0217 | EUR | IBS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0180 | EUR | IBS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0051 | EUR | IBS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0094 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0098 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01928 | hp2 | a0001 | c0002 | t0018 | g0136 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01934 | hp1 | a0001 | c0002 | t0012 | g0099 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01978 | hp2 | a0001 | c0002 | t0006 | g0258 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0220 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02145 | hp1 | a0001 | c0002 | t0011 | g0109 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0341 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02148 | hp2 | a0001 | c0002 | t0021 | g0089 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CDX | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02165 | hp2 | a0001 | c0002 | t0037 | g0115 | EAS | CDX | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02257 | hp1 | a0001 | c0002 | t0007 | g0113 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0059 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02258 | hp2 | a0001 | c0002 | t0007 | g0166 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0097 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02622 | hp1 | a0001 | c0002 | t0007 | g0119 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0338 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02647 | hp2 | a0001 | c0001 | t0033 | g0242 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0149 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0210 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0336 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0194 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0321 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02809 | hp1 | a0001 | c0001 | t0020 | g0225 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0245 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0247 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02896 | hp2 | a0001 | c0002 | t0007 | g0154 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0248 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02897 | hp2 | a0001 | c0002 | t0007 | g0155 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02970 | hp1 | a0001 | c0001 | t0031 | g0014 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0302 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0246 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03130 | hp1 | a0001 | c0002 | t0011 | g0111 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0340 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03453 | hp1 | a0002 | c0004 | t0011 | g0212 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0008 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03490 | hp2 | a0001 | c0002 | t0006 | g0001 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03492 | hp1 | a0001 | c0002 | t0006 | g0001 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03516 | hp1 | a0001 | c0001 | t0028 | g0011 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | ESN | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03540 | hp1 | a0001 | c0001 | t0020 | g0224 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03540 | hp2 | a0001 | c0002 | t0007 | g0211 | AFR | GWD | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0262 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0209 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0202 | SAS | PJL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03688 | hp1 | a0001 | c0002 | t0006 | g0263 | SAS | STU | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | STU | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | BEB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03831 | hp2 | a0001 | c0001 | t0027 | g0268 | SAS | BEB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03834 | hp1 | a0001 | c0001 | t0015 | g0055 | SAS | BEB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0148 | SAS | BEB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | STU | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | STU | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | STU | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | STU | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18522 | hp1 | a0001 | c0002 | t0007 | g0184 | AFR | YRI | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | YRI | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | CHB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | CHB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0104 | EAS | CHB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | CHB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18942 | hp1 | a0001 | c0001 | t0034 | g0025 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0190 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18980 | hp2 | a0001 | c0002 | t0024 | g0219 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18987 | hp1 | a0003 | c0003 | t0002 | g0324 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18988 | hp2 | a0001 | c0001 | t0013 | g0191 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18995 | hp2 | a0001 | c0001 | t0016 | g0062 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | LWK | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | LWK | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19043 | hp1 | a0001 | c0001 | t0023 | g0105 | AFR | LWK | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19055 | hp2 | a0001 | c0001 | t0013 | g0189 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19060 | hp2 | a0001 | c0001 | t0016 | g0066 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19068 | hp2 | a0001 | c0001 | t0016 | g0063 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19085 | hp2 | a0001 | c0001 | t0035 | g0054 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0010 | AFR | YRI | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | YRI | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA20129 | hp1 | a0001 | c0002 | t0012 | g0086 | AFR | ASW | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | ASW | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA20752 | hp1 | a0001 | c0001 | t0026 | g0145 | EUR | TSI | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA20752 | hp2 | a0001 | c0002 | t0006 | g0257 | EUR | TSI | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA20805 | hp1 | a0001 | c0002 | t0006 | g0256 | EUR | TSI | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0091 | EUR | TSI | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | CLM | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02109 | hp2 | a0001 | c0002 | t0011 | g0112 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02486 | hp1 | a0001 | c0001 | t0022 | g0235 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0339 | AFR | MSL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0337 | AFR | USA | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG06807 | hp2 | a0001 | c0001 | t0017 | g0303 | AFR | USA | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | USA | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | USA | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | LWK | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA21309 | hp2 | a0001 | c0001 | t0030 | g0201 | AFR | LWK | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0015 | g0153 | REF | REF | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0085 | REF | REF | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69571314
|
TTTAACAT others(21): Show |
T | 1 | a0003 | 1 | NA18987.hp1 | frameshift_variant | HIGH | c.294_321delTAACATGT others(20): Show |
p.Phe98fs | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/9 | 697/6768 | 294/1527 | 98/508 | INFO_REALIGN_3_PRIME | chr12 | 69571314 | |
| chr12:69574134
|
G | A | 1 | a0002 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.706G>A | p.Glu236Lys | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 1109/6768 | 706/1527 | 236/508 | chr12 | 69574134 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69574082
|
G | A | 2 | a0001c0002a0002c0004 | 120 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(117): Show |
synonymous_variant | LOW | c.654G>A | p.Ala218Ala | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 1057/6768 | 654/1527 | 218/508 | chr12 | 69574082 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69470390
|
A | G | 33 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | 302 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(299): Show |
5_prime_UTR_variant | MODIFIER | c.-401A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/9 | 98641 | chr12 | 69470390 | |||||
| chr12:69470414
|
G | A | 1 | a0001c0001t0017 | 2 | HG02976.hp1 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-377G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/9 | 98617 | chr12 | 69470414 | |||||
| chr12:69470450
|
A | G | 1 | a0001c0002t0007 | 8 | HG00741.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-341A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/9 | 98581 | chr12 | 69470450 | |||||
| chr12:69574973
|
T | G | 3 | a0001c0001t0013a0001c0002t0018a0001c0002t0024 | 6 | HG00408.hp1 HG01928.hp2 NA18946.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*18T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 18 | chr12 | 69574973 | |||||
| chr12:69575083
|
T | C | 1 | a0001c0002t0019 | 2 | HG00733.hp2 HG01070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*128T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 128 | chr12 | 69575083 | |||||
| chr12:69575165
|
C | T | 1 | a0001c0002t0037 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 210 | chr12 | 69575165 | |||||
| chr12:69575230
|
G | T | 4 | a0001c0001t0003a0001c0001t0034a0001c0001t0035others(1): Show | 69 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*275G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 275 | chr12 | 69575230 | |||||
| chr12:69575546
|
A | G | 1 | a0001c0001t0036 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 591 | chr12 | 69575546 | |||||
| chr12:69575752
|
C | T | 1 | a0001c0001t0033 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*797C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 797 | chr12 | 69575752 | |||||
| chr12:69576271
|
A | G | 1 | a0001c0002t0032 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1316A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 1316 | chr12 | 69576271 | |||||
| chr12:69576320
|
G | A | 1 | a0001c0001t0010 | 4 | HG00140.hp2 HG01169.hp2 HG01891.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1365G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 1365 | chr12 | 69576320 | |||||
| chr12:69576398
|
G | A | 4 | a0001c0001t0005a0001c0001t0014a0001c0001t0025others(1): Show | 18 | HG01109.hp2 HG01167.hp2 HG01361.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1443G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 1443 | chr12 | 69576398 | |||||
| chr12:69576629
|
C | T | 1 | a0001c0002t0024 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1674C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 1674 | chr12 | 69576629 | |||||
| chr12:69576733
|
T | G | 1 | a0001c0002t0021 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1778T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 1778 | chr12 | 69576733 | |||||
| chr12:69576810
|
C | G | 1 | a0001c0001t0016 | 3 | NA18995.hp2 NA19060.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1855C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 1855 | chr12 | 69576810 | |||||
| chr12:69577011
|
A | AT | 6 | a0001c0001t0005a0001c0001t0025a0001c0001t0029others(3): Show | 18 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2063dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 2064 | INFO_REALIGN_3_PRIME | chr12 | 69577011 | ||||
| chr12:69577194
|
A | T | 1 | a0001c0001t0035 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2239A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 2239 | chr12 | 69577194 | |||||
| chr12:69577305
|
T | C | 1 | a0001c0001t0014 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2350T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 2350 | chr12 | 69577305 | |||||
| chr12:69577487
|
A | G | 2 | a0001c0002t0006a0001c0002t0032 | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2532A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 2532 | chr12 | 69577487 | |||||
| chr12:69577670
|
A | C | 1 | a0001c0001t0025 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2715A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 2715 | chr12 | 69577670 | |||||
| chr12:69577694
|
G | A | 11 | a0001c0001t0001a0001c0002t0001a0001c0002t0007others(8): Show | 107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2739G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 2739 | chr12 | 69577694 | |||||
| chr12:69577720
|
C | T | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(28): Show | 238 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*2765C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 2765 | chr12 | 69577720 | |||||
| chr12:69577933
|
C | T | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(26): Show | 224 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*2978C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 2978 | chr12 | 69577933 | |||||
| chr12:69578272
|
G | T | 2 | a0001c0001t0023a0001c0001t0028 | 2 | HG03516.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3317G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 3317 | chr12 | 69578272 | |||||
| chr12:69578299
|
T | C | 1 | a0001c0001t0034 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3344T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 3344 | chr12 | 69578299 | |||||
| chr12:69578447
|
A | T | 2 | a0001c0002t0006a0001c0002t0032 | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3492A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 3492 | chr12 | 69578447 | |||||
| chr12:69578473
|
G | A | 1 | a0001c0001t0027 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3518G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 3518 | chr12 | 69578473 | |||||
| chr12:69578601
|
G | A | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | 308 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*3646G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 3646 | chr12 | 69578601 | |||||
| chr12:69578866
|
A | G | 2 | a0001c0001t0008a0001c0001t0020 | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3911A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 3911 | chr12 | 69578866 | |||||
| chr12:69578889
|
C | T | 1 | a0001c0001t0028 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3934C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 3934 | chr12 | 69578889 | |||||
| chr12:69579004
|
G | A | 2 | a0001c0001t0008a0001c0001t0020 | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4049G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 4049 | chr12 | 69579004 | |||||
| chr12:69579095
|
C | A | 2 | a0001c0002t0011a0002c0004t0011 | 4 | HG02109.hp2 HG02145.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4140C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 4140 | chr12 | 69579095 | |||||
| chr12:69579136
|
C | G | 1 | a0001c0001t0008 | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4181C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 4181 | chr12 | 69579136 | |||||
| chr12:69579227
|
C | T | 2 | a0001c0002t0006a0001c0002t0032 | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4272C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 4272 | chr12 | 69579227 | |||||
| chr12:69579412
|
CA | C | 14 | a0001c0001t0001a0001c0001t0009a0001c0001t0013others(11): Show | 117 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*4460delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 4460 | INFO_REALIGN_3_PRIME | chr12 | 69579412 | ||||
| chr12:69579424
|
A | G | 2 | a0001c0002t0006a0001c0002t0032 | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4469A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 4469 | chr12 | 69579424 | |||||
| chr12:69579567
|
T | C | 5 | a0001c0001t0002a0001c0001t0016a0001c0001t0017others(2): Show | 79 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4612T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 4612 | chr12 | 69579567 | |||||
| chr12:69579577
|
C | T | 2 | a0001c0001t0008a0001c0001t0020 | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4622C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 4622 | chr12 | 69579577 | |||||
| chr12:69579612
|
T | C | 16 | a0001c0001t0001a0001c0001t0009a0001c0001t0013others(13): Show | 119 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*4657T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 9/9 | 4657 | chr12 | 69579612 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69470594
|
C | T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+64C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69470594 | ||||||
| chr12:69470611
|
GGGATCCG others(6): Show |
G | 70 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0269others(67): Show | 70 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-261+84_-261+96del others(13): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69470611 | |||||
| chr12:69470628
|
C | G | 1 | a0001c0002t0001g0265 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-261+98C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69470628 | ||||||
| chr12:69470784
|
G | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+254G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69470784 | ||||||
| chr12:69470797
|
C | CCTCT | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+268_-261+271d others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69470797 | |||||
| chr12:69470805
|
C | G | 1 | a0001c0002t0001g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-261+275C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69470805 | ||||||
| chr12:69470847
|
C | T | 15 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-261+317C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69470847 | ||||||
| chr12:69470856
|
G | T | 68 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0271others(65): Show | 68 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-261+326G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69470856 | ||||||
| chr12:69470863
|
A | G | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+333A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69470863 | ||||||
| chr12:69471033
|
T | C | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+503T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69471033 | ||||||
| chr12:69471155
|
C | A | 1 | a0001c0001t0027g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-261+625C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69471155 | ||||||
| chr12:69471383
|
A | C | 1 | a0001c0002t0001g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-261+853A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69471383 | ||||||
| chr12:69471434
|
T | C | 15 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-261+904T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69471434 | ||||||
| chr12:69471521
|
G | C | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0271 | 3 | NA18946.hp2 NA18985.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-261+991G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69471521 | ||||||
| chr12:69472017
|
A | T | 7 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0229others(4): Show | 7 | HG00544.hp1 NA18955.hp2 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.-261+1487A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472017 | ||||||
| chr12:69472121
|
C | G | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+1591C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472121 | ||||||
| chr12:69472143
|
G | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+1613G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472143 | ||||||
| chr12:69472253
|
A | AT | 84 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(81): Show | 84 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.-261+1743dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69472253 | |||||
| chr12:69472253
|
A | ATT | 6 | a0001c0001t0002g0332a0001c0001t0002g0333a0001c0001t0002g0334others(3): Show | 6 | HG02027.hp1 HG02145.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+1742_-261+174 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69472253 | |||||
| chr12:69472253
|
A | T | 3 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223 | 3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-261+1723A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472253 | ||||||
| chr12:69472253
|
ATTTTTTT | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+1737_-261+174 others(11): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69472253 | |||||
| chr12:69472307
|
G | A | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+1777G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472307 | ||||||
| chr12:69472334
|
C | T | 108 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0013g0189others(105): Show | 108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-261+1804C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472334 | ||||||
| chr12:69472430
|
C | A | 308 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(305): Show | 309 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.-261+1900C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472430 | ||||||
| chr12:69472447
|
G | C | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-261+1917G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472447 | ||||||
| chr12:69472539
|
A | G | 1 | a0001c0001t0003g0076 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-261+2009A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472539 | ||||||
| chr12:69472600
|
G | A | 7 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(4): Show | 7 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-261+2070G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472600 | ||||||
| chr12:69472633
|
T | C | 1 | a0001c0002t0001g0108 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-261+2103T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472633 | ||||||
| chr12:69472688
|
G | A | 93 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(90): Show | 93 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.-261+2158G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472688 | ||||||
| chr12:69472889
|
C | T | 20 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(17): Show | 20 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-261+2359C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472889 | ||||||
| chr12:69472900
|
G | A | 2 | a0001c0001t0002g0278a0001c0001t0002g0279 | 2 | NA18961.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-261+2370G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472900 | ||||||
| chr12:69472908
|
G | A | 2 | a0001c0001t0020g0224a0001c0001t0020g0225 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-261+2378G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472908 | ||||||
| chr12:69473103
|
A | C | 20 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(17): Show | 20 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-261+2573A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473103 | ||||||
| chr12:69473113
|
T | C | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+2583T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473113 | ||||||
| chr12:69473133
|
G | C | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-261+2603G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473133 | ||||||
| chr12:69473264
|
C | G | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-261+2734C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473264 | ||||||
| chr12:69473476
|
T | G | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+2946T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473476 | ||||||
| chr12:69473556
|
T | G | 1 | a0001c0001t0004g0077 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-261+3026T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473556 | ||||||
| chr12:69473713
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-261+3183A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473713 | ||||||
| chr12:69473783
|
C | T | 5 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(2): Show | 5 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+3253C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473783 | ||||||
| chr12:69473796
|
C | T | 5 | a0001c0001t0002g0277a0001c0001t0002g0328a0001c0001t0002g0329others(2): Show | 5 | HG00609.hp2 HG00673.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+3266C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473796 | ||||||
| chr12:69473898
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-261+3368G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473898 | ||||||
| chr12:69473916
|
C | T | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+3386C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473916 | ||||||
| chr12:69473955
|
G | A | 4 | a0001c0001t0004g0078a0001c0001t0004g0079a0001c0001t0004g0080others(1): Show | 4 | NA18943.hp2 NA18968.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+3425G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473955 | ||||||
| chr12:69473967
|
C | T | 1 | a0001c0001t0003g0233 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-261+3437C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69473967 | ||||||
| chr12:69474009
|
A | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-261+3479A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474009 | ||||||
| chr12:69474031
|
C | T | 49 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(46): Show | 49 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.-261+3501C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474031 | ||||||
| chr12:69474032
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-261+3502G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474032 | ||||||
| chr12:69474043
|
A | G | 74 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(71): Show | 74 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.-261+3513A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474043 | ||||||
| chr12:69474127
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-261+3597C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474127 | ||||||
| chr12:69474327
|
G | A | 3 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035 | 3 | HG00735.hp1 HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-261+3797G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474327 | ||||||
| chr12:69474426
|
G | GA | 189 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(186): Show | 190 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.-261+3906dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69474426 | |||||
| chr12:69474541
|
A | C | 1 | a0001c0001t0004g0107 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-261+4011A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474541 | ||||||
| chr12:69474630
|
A | C | 113 | a0001c0001t0001g0226a0001c0001t0002g0204a0001c0001t0002g0205others(110): Show | 113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.-261+4100A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474630 | ||||||
| chr12:69474643
|
C | G | 1 | a0001c0002t0001g0200 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-261+4113C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474643 | ||||||
| chr12:69474685
|
A | C | 5 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+4155A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474685 | ||||||
| chr12:69474695
|
A | T | 1 | a0001c0002t0001g0194 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-261+4165A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474695 | ||||||
| chr12:69474773
|
A | G | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+4243A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474773 | ||||||
| chr12:69474816
|
G | C | 2 | a0001c0001t0020g0224a0001c0001t0020g0225 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-261+4286G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474816 | ||||||
| chr12:69474913
|
G | A | 307 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(304): Show | 308 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.-261+4383G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474913 | ||||||
| chr12:69474950
|
C | T | 1 | a0001c0001t0004g0106 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-261+4420C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69474950 | ||||||
| chr12:69475040
|
CAT | C | 107 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0013g0189others(104): Show | 107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-261+4513_-261+451 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69475040 | |||||
| chr12:69475335
|
AGTCCT | A | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+4808_-261+481 others(9): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69475335 | |||||
| chr12:69475410
|
A | T | 1 | a0001c0002t0001g0193 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-261+4880A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69475410 | ||||||
| chr12:69475856
|
G | T | 3 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075 | 3 | HG00733.hp1 HG01192.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-261+5326G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69475856 | ||||||
| chr12:69475924
|
C | T | 4 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0261others(1): Show | 5 | HG01106.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+5394C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69475924 | ||||||
| chr12:69476126
|
A | G | 35 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(32): Show | 36 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-261+5596A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476126 | ||||||
| chr12:69476173
|
C | T | 1 | a0001c0001t0023g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-261+5643C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476173 | ||||||
| chr12:69476241
|
C | T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+5711C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476241 | ||||||
| chr12:69476246
|
A | C | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+5716A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476246 | ||||||
| chr12:69476439
|
G | C | 131 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(128): Show | 131 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.-261+5909G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476439 | ||||||
| chr12:69476569
|
T | C | 2 | a0001c0001t0002g0278a0001c0001t0002g0279 | 2 | NA18961.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-261+6039T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476569 | ||||||
| chr12:69476660
|
A | G | 1 | a0001c0001t0023g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-261+6130A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476660 | ||||||
| chr12:69476753
|
C | CG | 18 | a0001c0001t0002g0266a0001c0001t0003g0017a0001c0001t0003g0036others(15): Show | 18 | HG00642.hp1 HG01192.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.-261+6232dupG | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69476753 | |||||
| chr12:69476753
|
CG | C | 221 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(218): Show | 222 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(219): Show |
intron_variant | MODIFIER | c.-261+6232delG | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69476753 | |||||
| chr12:69476759
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-261+6229G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476759 | ||||||
| chr12:69476770
|
G | C | 16 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(13): Show | 16 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-261+6240G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476770 | ||||||
| chr12:69476771
|
T | G | 1 | a0001c0002t0001g0193 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-261+6241T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476771 | ||||||
| chr12:69476772
|
G | T | 1 | a0001c0002t0001g0193 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-261+6242G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476772 | ||||||
| chr12:69476843
|
T | G | 71 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(68): Show | 71 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-261+6313T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69476843 | ||||||
| chr12:69477101
|
T | C | 2 | a0001c0001t0020g0224a0001c0001t0020g0225 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-261+6571T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477101 | ||||||
| chr12:69477101
|
TCCCAATG others(22): Show |
T | 5 | a0001c0002t0006g0256a0001c0002t0006g0257a0001c0002t0006g0258others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+6575_-261+660 others(33): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69477101 | |||||
| chr12:69477115
|
A | G | 1 | a0001c0001t0029g0206 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-261+6585A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477115 | ||||||
| chr12:69477128
|
G | T | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+6598G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477128 | ||||||
| chr12:69477272
|
C | CT | 8 | a0001c0001t0004g0078a0001c0001t0004g0079a0001c0001t0004g0080others(5): Show | 8 | HG01934.hp1 NA18943.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.-261+6763dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69477272 | |||||
| chr12:69477272
|
CT | C | 202 | a0001c0001t0001g0226a0001c0001t0002g0205a0001c0001t0002g0266others(199): Show | 203 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(200): Show |
intron_variant | MODIFIER | c.-261+6763delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69477272 | |||||
| chr12:69477272
|
CTT | C | 26 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0269others(23): Show | 26 | HG01934.hp2 HG01952.hp1 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-261+6762_-261+676 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69477272 | |||||
| chr12:69477366
|
C | T | 6 | a0001c0001t0005g0245a0001c0001t0005g0246a0001c0001t0005g0247others(3): Show | 6 | HG01109.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+6836C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477366 | ||||||
| chr12:69477406
|
A | C | 340 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-261+6876A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477406 | ||||||
| chr12:69477432
|
G | A | 10 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(7): Show | 10 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261+6902G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477432 | ||||||
| chr12:69477436
|
ACACGCCT others(451): Show |
A | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+6913_-261+737 others(4): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69477436 | |||||
| chr12:69477504
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+6974A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477504 | ||||||
| chr12:69477534
|
G | A | 2 | a0001c0001t0004g0077a0001c0001t0030g0201 | 2 | NA18985.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+7004G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477534 | ||||||
| chr12:69477572
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-261+7042G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477572 | ||||||
| chr12:69477635
|
C | G | 3 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191 | 3 | NA18946.hp1 NA18988.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-261+7105C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477635 | ||||||
| chr12:69477709
|
CTTAT | C | 96 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-261+7222_-261+722 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69477709 | |||||
| chr12:69477709
|
CTTATTTA others(1): Show |
C | 19 | a0001c0001t0003g0028a0001c0001t0003g0033a0001c0001t0003g0034others(16): Show | 20 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-261+7218_-261+722 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69477709 | |||||
| chr12:69477709
|
CTTATTTA others(5): Show |
C | 15 | a0001c0001t0005g0015a0001c0001t0009g0336a0001c0001t0009g0337others(12): Show | 15 | HG01167.hp2 HG01361.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-261+7214_-261+722 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69477709 | |||||
| chr12:69477709
|
CTTATTTA others(9): Show |
C | 182 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(179): Show | 182 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.-261+7210_-261+722 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69477709 | |||||
| chr12:69477709
|
CTTATTTA others(13): Show |
C | 1 | a0001c0001t0002g0282 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-261+7206_-261+722 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69477709 | |||||
| chr12:69477826
|
C | T | 12 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(9): Show | 12 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-261+7296C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477826 | ||||||
| chr12:69477943
|
A | G | 3 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007 | 3 | HG02622.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-261+7413A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477943 | ||||||
| chr12:69477963
|
A | G | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+7433A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477963 | ||||||
| chr12:69477988
|
A | G | 3 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007 | 3 | HG02622.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-261+7458A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69477988 | ||||||
| chr12:69478031
|
G | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+7501G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478031 | ||||||
| chr12:69478203
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-261+7673T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478203 | ||||||
| chr12:69478315
|
A | G | 108 | a0001c0001t0001g0226a0001c0001t0003g0176a0001c0001t0003g0177others(105): Show | 108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-261+7785A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478315 | ||||||
| chr12:69478392
|
A | G | 1 | a0001c0001t0016g0066 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-261+7862A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478392 | ||||||
| chr12:69478441
|
A | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-261+7911A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478441 | ||||||
| chr12:69478444
|
G | C | 227 | a0001c0001t0001g0226a0001c0001t0003g0016a0001c0001t0003g0017others(224): Show | 228 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-261+7914G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478444 | ||||||
| chr12:69478518
|
A | G | 1 | a0001c0002t0007g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-261+7988A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478518 | ||||||
| chr12:69478526
|
T | C | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+7996T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478526 | ||||||
| chr12:69478578
|
A | C | 1 | a0001c0001t0004g0104 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-261+8048A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478578 | ||||||
| chr12:69478724
|
A | ATG | 6 | a0001c0001t0004g0098a0001c0001t0010g0092a0001c0001t0010g0093others(3): Show | 6 | HG00140.hp2 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+8232_-261+823 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
A | ATGTG | 3 | a0001c0001t0004g0081a0001c0001t0005g0249a0001c0001t0005g0250 | 3 | HG01109.hp2 HG03098.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-261+8230_-261+823 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
A | ATGTGTG | 3 | a0001c0001t0005g0239a0001c0001t0005g0245a0001c0001t0030g0201 | 3 | HG02809.hp2 HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-261+8228_-261+823 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
A | ATGTGTGT others(1): Show |
5 | a0001c0001t0005g0240a0001c0001t0005g0241a0001c0001t0005g0246others(2): Show | 5 | HG02723.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+8226_-261+823 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
A | ATGTGTGT others(5): Show |
3 | a0001c0001t0005g0243a0001c0001t0005g0244a0001c0001t0033g0242 | 3 | HG02055.hp2 HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-261+8222_-261+823 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
A | G | 1 | a0001c0002t0021g0089 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-261+8194A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478724 | ||||||
| chr12:69478724
|
ATG | A | 30 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(27): Show | 30 | HG00673.hp2 HG01358.hp2 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.-261+8232_-261+823 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
ATGTG | A | 93 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0176others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-261+8230_-261+823 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
ATGTGTG | A | 59 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(56): Show | 59 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-261+8228_-261+823 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
ATGTGTGT others(1): Show |
A | 18 | a0001c0001t0002g0301a0001c0001t0002g0325a0001c0001t0002g0326others(15): Show | 18 | HG01884.hp1 HG02040.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-261+8226_-261+823 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
ATGTGTGT others(3): Show |
A | 86 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(83): Show | 87 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.-261+8224_-261+823 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0003g0227 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-261+8220_-261+823 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478724
|
ATGTGTGT others(9): Show |
A | 5 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02976.hp1 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+8218_-261+823 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69478724 | |||||
| chr12:69478730
|
G | A | 1 | a0001c0002t0007g0121 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-261+8200G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478730 | ||||||
| chr12:69478744
|
G | A | 2 | a0001c0001t0017g0302a0001c0001t0017g0303 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-261+8214G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69478744 | ||||||
| chr12:69479145
|
T | A | 1 | a0001c0002t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-261+8615T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479145 | ||||||
| chr12:69479377
|
T | C | 4 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0102others(1): Show | 4 | NA18971.hp2 NA18998.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+8847T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479377 | ||||||
| chr12:69479390
|
CT | C | 296 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(293): Show | 297 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.-261+8877delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69479390 | |||||
| chr12:69479405
|
T | C | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+8875T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479405 | ||||||
| chr12:69479407
|
T | C | 2 | a0001c0001t0003g0029a0001c0002t0001g0186 | 2 | HG03195.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-261+8877T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479407 | ||||||
| chr12:69479408
|
C | T | 2 | a0001c0001t0003g0029a0001c0002t0001g0186 | 2 | HG03195.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-261+8878C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479408 | ||||||
| chr12:69479409
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-261+8879T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479409 | ||||||
| chr12:69479427
|
C | T | 5 | a0001c0002t0001g0120a0001c0002t0011g0109a0001c0002t0011g0111others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+8897C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479427 | ||||||
| chr12:69479579
|
G | A | 2 | a0001c0002t0001g0180a0001c0002t0001g0217 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-261+9049G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479579 | ||||||
| chr12:69479666
|
G | T | 1 | a0001c0001t0003g0070 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-261+9136G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479666 | ||||||
| chr12:69479694
|
A | G | 2 | a0001c0001t0005g0012a0001c0001t0029g0206 | 2 | HG01069.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-261+9164A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479694 | ||||||
| chr12:69479944
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-261+9414C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69479944 | ||||||
| chr12:69480255
|
T | G | 1 | a0001c0001t0002g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-261+9725T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69480255 | ||||||
| chr12:69480391
|
G | A | 4 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+9861G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69480391 | ||||||
| chr12:69480526
|
G | A | 1 | a0001c0001t0029g0206 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-261+9996G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69480526 | ||||||
| chr12:69480820
|
T | C | 1 | a0001c0001t0002g0285 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-261+10290T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69480820 | ||||||
| chr12:69480919
|
C | T | 12 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(9): Show | 12 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-261+10389C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69480919 | ||||||
| chr12:69480931
|
TGTTA | T | 8 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0002t0001g0172others(5): Show | 8 | HG00639.hp2 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-261+10405_-261+10 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69480931 | |||||
| chr12:69481050
|
A | C | 1 | a0001c0002t0001g0199 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-261+10520A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481050 | ||||||
| chr12:69481238
|
C | T | 222 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(219): Show | 222 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.-261+10708C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481238 | ||||||
| chr12:69481281
|
AT | A | 130 | a0001c0001t0001g0226a0001c0001t0002g0275a0001c0001t0002g0286others(127): Show | 130 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.-261+10768delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69481281 | |||||
| chr12:69481317
|
G | A | 1 | a0001c0001t0002g0328 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-261+10787G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481317 | ||||||
| chr12:69481331
|
A | C | 2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-261+10801A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481331 | ||||||
| chr12:69481424
|
C | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+10894C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481424 | ||||||
| chr12:69481538
|
C | T | 1 | a0001c0001t0004g0104 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-261+11008C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481538 | ||||||
| chr12:69481587
|
C | T | 115 | a0001c0001t0001g0226a0001c0001t0002g0272a0001c0001t0003g0176others(112): Show | 115 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.-261+11057C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481587 | ||||||
| chr12:69481722
|
G | A | 2 | a0001c0002t0001g0195a0001c0002t0001g0196 | 2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-261+11192G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481722 | ||||||
| chr12:69481759
|
G | T | 1 | a0001c0002t0001g0170 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-261+11229G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481759 | ||||||
| chr12:69481936
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+11406A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481936 | ||||||
| chr12:69481976
|
G | A | 2 | a0001c0001t0017g0302a0001c0001t0017g0303 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-261+11446G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481976 | ||||||
| chr12:69481995
|
G | GT | 6 | a0001c0001t0002g0333a0001c0001t0003g0076a0001c0001t0005g0249others(3): Show | 6 | HG02055.hp1 HG03098.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+11478dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69481995 | |||||
| chr12:69482102
|
A | G | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-261+11572A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69482102 | ||||||
| chr12:69482397
|
G | A | 17 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(14): Show | 17 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-261+11867G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69482397 | ||||||
| chr12:69482658
|
T | G | 6 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0128others(3): Show | 6 | NA18954.hp2 NA18981.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+12128T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69482658 | ||||||
| chr12:69482861
|
T | C | 1 | a0001c0002t0011g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-261+12331T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69482861 | ||||||
| chr12:69483006
|
GCTAGTGC others(12): Show |
G | 1 | a0001c0002t0001g0171 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-261+12477_-261+12 others(25): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483006 | ||||||
| chr12:69483100
|
A | G | 6 | a0001c0001t0004g0077a0001c0001t0004g0078a0001c0001t0004g0079others(3): Show | 6 | NA18747.hp1 NA18943.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+12570A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483100 | ||||||
| chr12:69483171
|
A | G | 2 | a0001c0001t0005g0015a0001c0001t0031g0014 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-261+12641A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483171 | ||||||
| chr12:69483179
|
C | T | 306 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(303): Show | 307 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.-261+12649C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483179 | ||||||
| chr12:69483195
|
C | T | 5 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(2): Show | 5 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+12665C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483195 | ||||||
| chr12:69483356
|
G | A | 5 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(2): Show | 5 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+12826G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483356 | ||||||
| chr12:69483466
|
A | G | 102 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(99): Show | 102 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.-261+12936A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483466 | ||||||
| chr12:69483513
|
A | T | 116 | a0001c0001t0001g0226a0001c0001t0003g0176a0001c0001t0003g0177others(113): Show | 116 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.-261+12983A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483513 | ||||||
| chr12:69483561
|
A | G | 1 | a0001c0002t0012g0083 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-261+13031A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483561 | ||||||
| chr12:69483570
|
T | C | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG00140.hp1 HG00733.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+13040T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483570 | ||||||
| chr12:69483650
|
C | T | 3 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0169 | 3 | HG02970.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-261+13120C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483650 | ||||||
| chr12:69483817
|
A | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-261+13287A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483817 | ||||||
| chr12:69483826
|
T | G | 1 | a0001c0002t0001g0181 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-261+13296T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69483826 | ||||||
| chr12:69483829
|
TTTAATCT others(19): Show |
T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+13302_-261+13 others(32): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69483829 | |||||
| chr12:69484095
|
C | CTTTTTTT others(5): Show |
12 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(9): Show | 13 | HG00639.hp1 HG00642.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+13574_-261+13 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69484095 | |||||
| chr12:69484095
|
C | CTTTTTTT others(6): Show |
2 | a0001c0002t0006g0253a0001c0002t0006g0258 | 2 | HG00741.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-261+13574_-261+13 others(19): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69484095 | |||||
| chr12:69484115
|
C | T | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+13585C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69484115 | ||||||
| chr12:69484116
|
G | T | 1 | a0001c0002t0001g0130 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-261+13586G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69484116 | ||||||
| chr12:69484152
|
T | A | 1 | a0001c0002t0001g0171 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-261+13622T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69484152 | ||||||
| chr12:69484339
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+13809C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69484339 | ||||||
| chr12:69484858
|
A | G | 1 | a0001c0001t0029g0206 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-261+14328A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69484858 | ||||||
| chr12:69484940
|
G | T | 1 | a0001c0001t0003g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-261+14410G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69484940 | ||||||
| chr12:69484964
|
T | G | 2 | a0001c0002t0001g0131a0001c0002t0001g0192 | 2 | NA18961.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-261+14434T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69484964 | ||||||
| chr12:69485004
|
G | C | 3 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0070 | 3 | HG02451.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-261+14474G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485004 | ||||||
| chr12:69485035
|
C | A | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-261+14505C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485035 | ||||||
| chr12:69485082
|
A | AAC | 13 | a0001c0001t0003g0018a0001c0001t0003g0029a0001c0001t0003g0058others(10): Show | 13 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+14605_-261+14 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
A | AACAC | 14 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0032others(11): Show | 14 | HG00673.hp2 HG01192.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.-261+14603_-261+14 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
A | AACACAC | 14 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0034others(11): Show | 14 | HG01346.hp1 HG01358.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.-261+14601_-261+14 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
A | AACACACA others(1): Show |
12 | a0001c0001t0003g0033a0001c0001t0003g0036a0001c0001t0003g0037others(9): Show | 12 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.-261+14599_-261+14 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
A | AACACACA others(3): Show |
6 | a0001c0001t0003g0020a0001c0001t0003g0035a0001c0001t0003g0039others(3): Show | 6 | HG01496.hp2 HG02148.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+14597_-261+14 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
A | AACACACA others(5): Show |
7 | a0001c0001t0003g0016a0001c0001t0003g0042a0001c0001t0003g0049others(4): Show | 7 | HG02040.hp1 HG02970.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.-261+14595_-261+14 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
A | AACACACA others(7): Show |
2 | a0001c0001t0017g0303a0001c0002t0007g0119 | 2 | HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-261+14593_-261+14 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
A | AACACACA others(9): Show |
3 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0002t0001g0139 | 3 | HG02074.hp1 HG04228.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.-261+14591_-261+14 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
A | AACACACA others(11): Show |
2 | a0001c0001t0017g0302a0001c0002t0001g0167 | 2 | HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-261+14589_-261+14 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
A | AACACACA others(15): Show |
2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | NA18991.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-261+14585_-261+14 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
A | ACACACAC others(4): Show |
1 | a0001c0002t0007g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-261+14552_-261+14 others(17): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485082 | ||||||
| chr12:69485082
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0009g0340 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-261+14552_-261+14 others(19): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485082 | ||||||
| chr12:69485082
|
A | ACACACAC others(10): Show |
2 | a0001c0002t0001g0165a0001c0002t0001g0181 | 2 | HG04228.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-261+14552_-261+14 others(23): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485082 | ||||||
| chr12:69485082
|
A | ACACACAC others(12): Show |
2 | a0001c0002t0001g0129a0001c0002t0001g0186 | 2 | NA18994.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-261+14552_-261+14 others(25): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485082 | ||||||
| chr12:69485082
|
AAC | A | 16 | a0001c0001t0003g0026a0001c0001t0003g0044a0001c0001t0003g0045others(13): Show | 16 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-261+14605_-261+14 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
AACAC | A | 9 | a0001c0001t0003g0017a0001c0001t0003g0232a0001c0001t0004g0096others(6): Show | 9 | HG00639.hp1 HG00741.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+14603_-261+14 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
AACACAC | A | 7 | a0001c0001t0003g0021a0001c0001t0003g0227a0001c0001t0003g0233others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-261+14601_-261+14 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
AACACACA others(3): Show |
A | 3 | a0001c0001t0014g0009a0001c0001t0014g0010a0001c0002t0001g0200 | 3 | HG01167.hp2 NA18959.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-261+14597_-261+14 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
AACACACA others(5): Show |
A | 1 | a0001c0001t0008g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-261+14595_-261+14 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
AACACACA others(7): Show |
A | 6 | a0001c0001t0008g0003a0001c0001t0008g0004a0001c0001t0008g0005others(3): Show | 6 | HG02559.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+14593_-261+14 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485082
|
AACACACA others(17): Show |
A | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-261+14583_-261+14 others(30): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485082 | |||||
| chr12:69485083
|
A | ACACACAC others(25): Show |
3 | a0001c0001t0002g0289a0001c0001t0002g0306a0001c0001t0002g0307 | 3 | HG01934.hp2 NA19012.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-261+14582_-261+14 others(38): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485083 | |||||
| chr12:69485085
|
A | ACACACAC others(25): Show |
1 | a0001c0001t0002g0334 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-261+14584_-261+14 others(38): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485085 | |||||
| chr12:69485085
|
A | ACACACAC others(21): Show |
1 | a0001c0001t0002g0305 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-261+14582_-261+14 others(34): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485085 | |||||
| chr12:69485085
|
A | ACACACAC others(23): Show |
12 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0269others(9): Show | 12 | HG00558.hp1 HG00597.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.-261+14582_-261+14 others(36): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485085 | |||||
| chr12:69485085
|
A | ACACACAC others(21): Show |
3 | a0001c0001t0002g0304a0001c0001t0002g0322a0003c0003t0002g0324 | 3 | NA18987.hp1 NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-261+14580_-261+14 others(34): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485085 | |||||
| chr12:69485085
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0002g0284 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-261+14578_-261+14 others(32): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485085 | |||||
| chr12:69485087
|
A | ACACACAC others(21): Show |
2 | a0001c0001t0002g0287a0001c0001t0002g0327 | 2 | NA18942.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-261+14584_-261+14 others(34): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485087 | |||||
| chr12:69485087
|
A | ACACACAC others(21): Show |
29 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(26): Show | 29 | HG01952.hp1 HG02040.hp2 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.-261+14582_-261+14 others(34): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485087 | |||||
| chr12:69485087
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0002g0271 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-261+14580_-261+14 others(32): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485087 | |||||
| chr12:69485087
|
A | ACACACAC others(15): Show |
2 | a0001c0001t0002g0283a0001c0001t0002g0285 | 2 | HG02071.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-261+14576_-261+14 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485087 | |||||
| chr12:69485089
|
A | ACACACAC others(19): Show |
13 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0274others(10): Show | 13 | HG00609.hp2 HG00673.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.-261+14582_-261+14 others(32): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485089 | |||||
| chr12:69485089
|
A | ACACACAC others(21): Show |
2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-261+14582_-261+14 others(34): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485089 | |||||
| chr12:69485089
|
A | ACACACAC others(17): Show |
1 | a0001c0001t0002g0323 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-261+14580_-261+14 others(30): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485089 | |||||
| chr12:69485091
|
A | ACACACAC others(21): Show |
1 | a0001c0001t0002g0288 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-261+14584_-261+14 others(34): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485091 | |||||
| chr12:69485091
|
A | ACACACAC others(17): Show |
1 | a0001c0001t0002g0270 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-261+14582_-261+14 others(30): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485091 | |||||
| chr12:69485091
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0002g0282 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-261+14582_-261+14 others(32): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485091 | |||||
| chr12:69485093
|
A | ACACACAC others(15): Show |
1 | a0001c0001t0002g0300 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-261+14582_-261+14 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485093 | |||||
| chr12:69485095
|
A | ACACACAC others(13): Show |
1 | a0001c0001t0033g0242 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-261+14582_-261+14 others(26): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485095 | |||||
| chr12:69485097
|
A | ACACACAC others(41): Show |
1 | a0001c0001t0029g0206 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-261+14586_-261+14 others(54): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485097 | |||||
| chr12:69485097
|
A | ACACACAC others(11): Show |
13 | a0001c0001t0002g0301a0001c0001t0003g0236a0001c0001t0003g0237others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+14582_-261+14 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485097 | |||||
| chr12:69485097
|
A | ACACACAC others(39): Show |
1 | a0001c0001t0005g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-261+14582_-261+14 others(52): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485097 | |||||
| chr12:69485097
|
A | ACACACAC others(9): Show |
2 | a0001c0001t0005g0247a0001c0001t0005g0248 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-261+14580_-261+14 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485097 | |||||
| chr12:69485099
|
A | ACACACAC others(9): Show |
1 | a0001c0001t0003g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-261+14582_-261+14 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485099 | |||||
| chr12:69485099
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0025g0013 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-261+14580_-261+14 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485099 | |||||
| chr12:69485101
|
A | ACACACAC others(18): Show |
1 | a0001c0002t0001g0171 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-261+14572_-261+14 others(31): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485101 | |||||
| chr12:69485101
|
A | ACACACAC others(15): Show |
2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-261+14586_-261+14 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485101 | |||||
| chr12:69485101
|
A | ACACACAC others(11): Show |
2 | a0001c0001t0005g0015a0001c0001t0031g0014 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-261+14584_-261+14 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485101 | |||||
| chr12:69485134
|
C | CACACACA others(21): Show |
1 | a0001c0002t0001g0172 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-261+14606_-261+14 others(34): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACACA others(17): Show |
3 | a0001c0002t0001g0126a0001c0002t0001g0130a0001c0002t0001g0134 | 3 | NA18952.hp1 NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-261+14606_-261+14 others(30): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACACA others(15): Show |
3 | a0001c0002t0001g0135a0001c0002t0001g0173a0001c0002t0001g0197 | 3 | HG02109.hp1 HG02615.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-261+14606_-261+14 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACACA others(13): Show |
8 | a0001c0002t0001g0137a0001c0002t0001g0138a0001c0002t0001g0180others(5): Show | 8 | HG00609.hp1 HG01516.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.-261+14606_-261+14 others(26): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACACA others(11): Show |
13 | a0001c0002t0001g0114a0001c0002t0001g0127a0001c0002t0001g0131others(10): Show | 13 | HG00544.hp2 HG00639.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+14606_-261+14 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACACA others(9): Show |
11 | a0001c0001t0026g0145a0001c0002t0001g0108a0001c0002t0001g0144others(8): Show | 11 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(8): Show |
intron_variant | MODIFIER | c.-261+14606_-261+14 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACACA others(7): Show |
9 | a0001c0001t0023g0105a0001c0002t0001g0110a0001c0002t0001g0123others(6): Show | 9 | HG00597.hp1 HG00735.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+14606_-261+14 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACACA others(5): Show |
10 | a0001c0001t0013g0189a0001c0001t0013g0191a0001c0002t0001g0122others(7): Show | 10 | HG00741.hp2 HG02055.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.-261+14606_-261+14 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACACA others(7): Show |
1 | a0001c0002t0001g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-261+14606_-261+14 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACACA others(3): Show |
10 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0013g0190others(7): Show | 10 | HG02257.hp2 HG02486.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261+14606_-261+14 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACACA others(1): Show |
12 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0341others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-261+14606_-261+14 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CACACAT | 10 | a0001c0001t0009g0338a0001c0001t0009g0339a0001c0002t0001g0159others(7): Show | 10 | HG01123.hp1 HG01258.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261+14606_-261+14 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | CAT | 5 | a0001c0001t0020g0224a0001c0002t0001g0118a0001c0002t0001g0251others(2): Show | 5 | HG02135.hp1 HG03540.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+14605_-261+14 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485134 | |||||
| chr12:69485134
|
C | T | 132 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(129): Show | 133 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.-261+14604C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485134 | ||||||
| chr12:69485172
|
C | CTTAT | 25 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(22): Show | 25 | HG00140.hp1 HG00544.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.-261+14665_-261+14 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485172 | |||||
| chr12:69485172
|
CTTAT | C | 229 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(226): Show | 229 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(226): Show |
intron_variant | MODIFIER | c.-261+14665_-261+14 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69485172 | |||||
| chr12:69485243
|
C | T | 5 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02976.hp1 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+14713C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485243 | ||||||
| chr12:69485244
|
G | A | 4 | a0001c0002t0001g0159a0001c0002t0001g0164a0001c0002t0001g0182others(1): Show | 4 | HG01346.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+14714G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485244 | ||||||
| chr12:69485283
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-261+14753C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485283 | ||||||
| chr12:69485327
|
C | T | 1 | a0001c0001t0002g0321 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-261+14797C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485327 | ||||||
| chr12:69485331
|
C | T | 1 | a0001c0001t0004g0084 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-261+14801C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485331 | ||||||
| chr12:69485444
|
A | C | 228 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(225): Show | 228 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(225): Show |
intron_variant | MODIFIER | c.-261+14914A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485444 | ||||||
| chr12:69485444
|
A | T | 1 | a0001c0001t0005g0239 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-261+14914A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485444 | ||||||
| chr12:69485463
|
T | A | 1 | a0001c0001t0002g0272 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-261+14933T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485463 | ||||||
| chr12:69485472
|
G | A | 1 | a0001c0001t0008g0003 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-261+14942G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485472 | ||||||
| chr12:69485474
|
G | A | 18 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(15): Show | 18 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-261+14944G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485474 | ||||||
| chr12:69485564
|
C | T | 1 | a0001c0001t0003g0050 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-261+15034C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485564 | ||||||
| chr12:69485572
|
T | C | 1 | a0001c0002t0001g0171 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-261+15042T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485572 | ||||||
| chr12:69485574
|
C | T | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+15044C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485574 | ||||||
| chr12:69485593
|
C | T | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+15063C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485593 | ||||||
| chr12:69485653
|
A | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-261+15123A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485653 | ||||||
| chr12:69485673
|
G | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+15143G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485673 | ||||||
| chr12:69485707
|
A | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-261+15177A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485707 | ||||||
| chr12:69485795
|
A | G | 1 | a0001c0002t0001g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-261+15265A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485795 | ||||||
| chr12:69485965
|
G | A | 94 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0013g0189others(91): Show | 94 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-261+15435G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69485965 | ||||||
| chr12:69486013
|
A | G | 1 | a0001c0002t0007g0211 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-261+15483A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69486013 | ||||||
| chr12:69486103
|
T | C | 113 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0009g0336others(110): Show | 113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.-261+15573T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69486103 | ||||||
| chr12:69486182
|
A | AT | 10 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191others(7): Show | 10 | HG01069.hp1 HG01361.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261+15666dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69486182 | |||||
| chr12:69486182
|
A | ATT | 69 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0005g0012others(66): Show | 70 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-261+15665_-261+15 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69486182 | |||||
| chr12:69486182
|
A | ATTT | 46 | a0001c0001t0026g0145a0001c0002t0001g0108a0001c0002t0001g0122others(43): Show | 46 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-261+15664_-261+15 others(9): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69486182 | |||||
| chr12:69486182
|
AT | A | 71 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0272others(68): Show | 71 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-261+15666delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69486182 | |||||
| chr12:69486306
|
C | CA | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+15777dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69486306 | |||||
| chr12:69486390
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+15860A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69486390 | ||||||
| chr12:69486569
|
A | C | 1 | a0001c0002t0012g0086 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-261+16039A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69486569 | ||||||
| chr12:69486579
|
C | A | 4 | a0001c0002t0001g0159a0001c0002t0001g0164a0001c0002t0001g0182others(1): Show | 4 | HG01346.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+16049C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69486579 | ||||||
| chr12:69486848
|
C | T | 229 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(226): Show | 229 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(226): Show |
intron_variant | MODIFIER | c.-261+16318C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69486848 | ||||||
| chr12:69486882
|
A | C | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+16352A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69486882 | ||||||
| chr12:69487079
|
A | G | 243 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(240): Show | 244 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(241): Show |
intron_variant | MODIFIER | c.-261+16549A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69487079 | ||||||
| chr12:69487179
|
T | A | 66 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(63): Show | 66 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-261+16649T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69487179 | ||||||
| chr12:69487397
|
A | T | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-261+16867A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69487397 | ||||||
| chr12:69487458
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+16928C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69487458 | ||||||
| chr12:69487543
|
C | G | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+17013C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69487543 | ||||||
| chr12:69487594
|
T | C | 5 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(2): Show | 5 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+17064T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69487594 | ||||||
| chr12:69487720
|
C | T | 1 | a0001c0001t0029g0206 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-261+17190C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69487720 | ||||||
| chr12:69487948
|
C | T | 1 | a0001c0002t0001g0174 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-261+17418C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69487948 | ||||||
| chr12:69487999
|
A | G | 1 | a0001c0001t0002g0320 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-261+17469A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69487999 | ||||||
| chr12:69488061
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-261+17531T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488061 | ||||||
| chr12:69488221
|
T | C | 1 | a0001c0002t0006g0001 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-261+17691T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488221 | ||||||
| chr12:69488360
|
A | G | 5 | a0001c0002t0001g0120a0001c0002t0011g0109a0001c0002t0011g0111others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+17830A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488360 | ||||||
| chr12:69488457
|
G | A | 305 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(302): Show | 306 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.-261+17927G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488457 | ||||||
| chr12:69488533
|
T | C | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+18003T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488533 | ||||||
| chr12:69488544
|
C | T | 308 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(305): Show | 309 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.-261+18014C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488544 | ||||||
| chr12:69488643
|
T | G | 1 | a0001c0001t0027g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-261+18113T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488643 | ||||||
| chr12:69488708
|
C | T | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+18178C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488708 | ||||||
| chr12:69488755
|
T | C | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+18225T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488755 | ||||||
| chr12:69488777
|
C | T | 1 | a0001c0001t0003g0228 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-261+18247C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488777 | ||||||
| chr12:69488833
|
G | T | 4 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010others(1): Show | 4 | HG01167.hp2 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+18303G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488833 | ||||||
| chr12:69488835
|
A | C | 1 | a0001c0001t0002g0307 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-261+18305A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488835 | ||||||
| chr12:69488842
|
G | C | 1 | a0001c0001t0003g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-261+18312G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488842 | ||||||
| chr12:69488853
|
T | C | 1 | a0001c0001t0002g0334 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-261+18323T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488853 | ||||||
| chr12:69488931
|
C | G | 25 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(22): Show | 25 | HG01069.hp1 HG01109.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.-261+18401C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69488931 | ||||||
| chr12:69489124
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-261+18594C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69489124 | ||||||
| chr12:69489299
|
T | C | 2 | a0001c0002t0001g0135a0001c0002t0001g0213 | 2 | HG00609.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-261+18769T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69489299 | ||||||
| chr12:69489331
|
G | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-261+18801G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69489331 | ||||||
| chr12:69489408
|
G | A | 1 | a0001c0002t0001g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-261+18878G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69489408 | ||||||
| chr12:69489471
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+18941A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69489471 | ||||||
| chr12:69489579
|
A | G | 21 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(18): Show | 21 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.-261+19049A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69489579 | ||||||
| chr12:69489618
|
T | A | 4 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+19088T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69489618 | ||||||
| chr12:69489654
|
G | A | 73 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(70): Show | 73 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-261+19124G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69489654 | ||||||
| chr12:69489668
|
C | CA | 12 | a0001c0001t0003g0238a0001c0001t0005g0240a0001c0001t0008g0005others(9): Show | 12 | HG00558.hp2 HG02135.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-261+19154dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69489668 | |||||
| chr12:69489668
|
CA | C | 72 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(69): Show | 72 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.-261+19154delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69489668 | |||||
| chr12:69489763
|
A | G | 1 | a0001c0001t0002g0312 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-261+19233A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69489763 | ||||||
| chr12:69489776
|
A | G | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-261+19246A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69489776 | ||||||
| chr12:69489816
|
G | GT | 15 | a0001c0001t0025g0013a0001c0002t0001g0262a0001c0002t0006g0001others(12): Show | 16 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-261+19297dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69489816 | |||||
| chr12:69489816
|
G | GTT | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+19296_-261+19 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69489816 | |||||
| chr12:69489816
|
GT | G | 73 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0208others(70): Show | 73 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-261+19297delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69489816 | |||||
| chr12:69490005
|
C | T | 105 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0013g0189others(102): Show | 105 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.-261+19475C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69490005 | ||||||
| chr12:69490141
|
G | T | 306 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(303): Show | 307 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.-261+19611G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69490141 | ||||||
| chr12:69490192
|
G | C | 1 | a0001c0001t0003g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-261+19662G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69490192 | ||||||
| chr12:69490431
|
GT | G | 221 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(218): Show | 222 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(219): Show |
intron_variant | MODIFIER | c.-261+19917delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69490431 | |||||
| chr12:69490431
|
GTT | G | 6 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0022g0235others(3): Show | 6 | HG02486.hp1 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.-261+19916_-261+19 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69490431 | |||||
| chr12:69490715
|
G | T | 5 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(2): Show | 5 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+20185G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69490715 | ||||||
| chr12:69491044
|
T | C | 1 | a0001c0002t0007g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-261+20514T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491044 | ||||||
| chr12:69491210
|
C | T | 1 | a0001c0001t0023g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-261+20680C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491210 | ||||||
| chr12:69491284
|
C | T | 1 | a0001c0001t0003g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-261+20754C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491284 | ||||||
| chr12:69491294
|
C | T | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-261+20764C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491294 | ||||||
| chr12:69491343
|
A | T | 7 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0229others(4): Show | 7 | HG00544.hp1 NA18955.hp2 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.-261+20813A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491343 | ||||||
| chr12:69491365
|
C | A | 233 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(230): Show | 234 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(231): Show |
intron_variant | MODIFIER | c.-261+20835C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491365 | ||||||
| chr12:69491378
|
T | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+20848T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491378 | ||||||
| chr12:69491388
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-261+20858C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491388 | ||||||
| chr12:69491505
|
A | AT | 91 | a0001c0001t0001g0226a0001c0001t0003g0177a0001c0001t0008g0005others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.-261+20999dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69491505 | |||||
| chr12:69491505
|
A | ATT | 10 | a0001c0001t0026g0145a0001c0001t0030g0201a0001c0002t0001g0114others(7): Show | 10 | HG00544.hp2 HG02135.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-261+20998_-261+20 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69491505 | |||||
| chr12:69491505
|
AT | A | 124 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0208others(121): Show | 125 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-261+20999delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69491505 | |||||
| chr12:69491505
|
ATT | A | 80 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(77): Show | 80 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-261+20998_-261+20 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69491505 | |||||
| chr12:69491533
|
G | T | 5 | a0001c0002t0001g0120a0001c0002t0011g0109a0001c0002t0011g0111others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+21003G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491533 | ||||||
| chr12:69491555
|
C | T | 1 | a0001c0001t0002g0305 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-261+21025C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491555 | ||||||
| chr12:69491634
|
A | G | 112 | a0001c0001t0001g0226a0001c0001t0003g0176a0001c0001t0003g0177others(109): Show | 112 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.-261+21104A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491634 | ||||||
| chr12:69491727
|
G | T | 1 | a0001c0001t0005g0239 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-261+21197G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491727 | ||||||
| chr12:69491893
|
T | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+21363T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491893 | ||||||
| chr12:69491905
|
C | T | 1 | a0001c0001t0002g0287 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-261+21375C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69491905 | ||||||
| chr12:69492032
|
A | G | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+21502A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69492032 | ||||||
| chr12:69492242
|
G | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+21712G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69492242 | ||||||
| chr12:69492251
|
T | C | 1 | a0001c0001t0005g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-261+21721T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69492251 | ||||||
| chr12:69492348
|
A | G | 1 | a0001c0001t0034g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-261+21818A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69492348 | ||||||
| chr12:69492408
|
T | G | 1 | a0001c0001t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-261+21878T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69492408 | ||||||
| chr12:69492555
|
G | A | 4 | a0001c0002t0011g0109a0001c0002t0011g0111a0001c0002t0011g0112others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+22025G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69492555 | ||||||
| chr12:69492700
|
T | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-261+22170T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69492700 | ||||||
| chr12:69492719
|
A | G | 1 | a0001c0001t0002g0316 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-261+22189A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69492719 | ||||||
| chr12:69492798
|
T | G | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-261+22268T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69492798 | ||||||
| chr12:69493007
|
T | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+22477T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493007 | ||||||
| chr12:69493017
|
T | G | 1 | a0001c0002t0001g0165 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-261+22487T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493017 | ||||||
| chr12:69493023
|
T | G | 4 | a0001c0001t0005g0240a0001c0001t0005g0243a0001c0001t0005g0244others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+22493T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493023 | ||||||
| chr12:69493069
|
A | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-261+22539A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493069 | ||||||
| chr12:69493098
|
G | A | 1 | a0001c0001t0002g0330 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-261+22568G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493098 | ||||||
| chr12:69493197
|
T | C | 3 | a0001c0001t0023g0105a0001c0002t0001g0172a0001c0002t0001g0220 | 3 | HG02055.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-261+22667T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493197 | ||||||
| chr12:69493269
|
A | G | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+22739A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493269 | ||||||
| chr12:69493341
|
A | G | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+22811A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493341 | ||||||
| chr12:69493448
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+22918C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493448 | ||||||
| chr12:69493456
|
C | T | 3 | a0001c0001t0016g0062a0001c0001t0016g0063a0001c0001t0016g0066 | 3 | NA18995.hp2 NA19060.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-261+22926C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493456 | ||||||
| chr12:69493594
|
G | A | 2 | a0001c0002t0001g0172a0001c0002t0001g0220 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-261+23064G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493594 | ||||||
| chr12:69493604
|
C | T | 21 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(18): Show | 21 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.-261+23074C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493604 | ||||||
| chr12:69493617
|
T | A | 243 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(240): Show | 244 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(241): Show |
intron_variant | MODIFIER | c.-261+23087T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493617 | ||||||
| chr12:69494037
|
G | A | 115 | a0001c0001t0001g0226a0001c0001t0003g0176a0001c0001t0003g0177others(112): Show | 115 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.-261+23507G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494037 | ||||||
| chr12:69494350
|
C | G | 243 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(240): Show | 244 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(241): Show |
intron_variant | MODIFIER | c.-261+23820C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494350 | ||||||
| chr12:69494367
|
T | C | 243 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(240): Show | 244 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(241): Show |
intron_variant | MODIFIER | c.-261+23837T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494367 | ||||||
| chr12:69494450
|
A | C | 1 | a0001c0001t0002g0335 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-261+23920A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494450 | ||||||
| chr12:69494450
|
A | G | 4 | a0001c0001t0003g0026a0001c0001t0003g0030a0001c0001t0003g0031others(1): Show | 4 | HG00673.hp2 NA18960.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+23920A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494450 | ||||||
| chr12:69494521
|
G | C | 1 | a0001c0002t0037g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-261+23991G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494521 | ||||||
| chr12:69494702
|
G | T | 1 | a0001c0002t0012g0099 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-261+24172G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494702 | ||||||
| chr12:69494703
|
C | G | 1 | a0001c0002t0012g0099 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-261+24173C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494703 | ||||||
| chr12:69494711
|
A | C | 1 | a0001c0002t0001g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-261+24181A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494711 | ||||||
| chr12:69494893
|
C | A | 1 | a0001c0001t0005g0239 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-261+24363C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494893 | ||||||
| chr12:69494991
|
C | G | 1 | a0001c0002t0001g0156 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-261+24461C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494991 | ||||||
| chr12:69495028
|
C | T | 2 | a0001c0001t0003g0016a0001c0001t0003g0058 | 2 | HG00408.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.-261+24498C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495028 | ||||||
| chr12:69495069
|
C | T | 1 | a0001c0001t0003g0231 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-261+24539C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495069 | ||||||
| chr12:69495095
|
C | T | 3 | a0001c0002t0001g0110a0001c0002t0001g0114a0001c0002t0001g0234 | 3 | HG00544.hp2 HG02083.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-261+24565C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495095 | ||||||
| chr12:69495104
|
C | T | 308 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(305): Show | 309 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.-261+24574C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495104 | ||||||
| chr12:69495198
|
C | T | 29 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238others(26): Show | 29 | HG01069.hp1 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.-261+24668C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495198 | ||||||
| chr12:69495390
|
G | C | 1 | a0001c0001t0004g0106 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-261+24860G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495390 | ||||||
| chr12:69495547
|
G | A | 6 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0128others(3): Show | 6 | NA18954.hp2 NA18981.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+25017G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495547 | ||||||
| chr12:69495785
|
G | A | 3 | a0001c0002t0001g0197a0001c0002t0001g0198a0001c0002t0001g0199 | 3 | HG01884.hp2 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-261+25255G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495785 | ||||||
| chr12:69495822
|
A | T | 4 | a0001c0001t0002g0308a0001c0001t0002g0318a0001c0001t0002g0319others(1): Show | 4 | NA18971.hp1 NA18980.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-261+25292A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495822 | ||||||
| chr12:69495890
|
C | T | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-261+25360C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495890 | ||||||
| chr12:69495928
|
A | G | 2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG00639.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-261+25398A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495928 | ||||||
| chr12:69495932
|
A | G | 117 | a0001c0001t0001g0226a0001c0001t0003g0176a0001c0001t0003g0177others(114): Show | 117 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.-261+25402A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69495932 | ||||||
| chr12:69496053
|
A | G | 1 | a0001c0002t0012g0099 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-261+25523A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496053 | ||||||
| chr12:69496056
|
A | G | 117 | a0001c0001t0001g0226a0001c0001t0003g0176a0001c0001t0003g0177others(114): Show | 117 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.-261+25526A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496056 | ||||||
| chr12:69496117
|
A | G | 1 | a0001c0001t0004g0106 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-261+25587A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496117 | ||||||
| chr12:69496127
|
A | G | 2 | a0001c0002t0001g0182a0001c0002t0001g0185 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-261+25597A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496127 | ||||||
| chr12:69496264
|
G | A | 4 | a0001c0001t0003g0228a0001c0002t0001g0197a0001c0002t0001g0198others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-261+25734G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496264 | ||||||
| chr12:69496333
|
C | T | 2 | a0001c0002t0006g0259a0001c0002t0006g0260 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-261+25803C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496333 | ||||||
| chr12:69496462
|
T | C | 1 | a0001c0001t0002g0297 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-261+25932T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496462 | ||||||
| chr12:69496514
|
A | G | 2 | a0001c0001t0003g0051a0001c0001t0036g0046 | 2 | HG00140.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-261+25984A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496514 | ||||||
| chr12:69496618
|
G | T | 1 | a0001c0001t0025g0013 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-261+26088G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496618 | ||||||
| chr12:69496714
|
T | G | 1 | a0001c0001t0003g0034 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-261+26184T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496714 | ||||||
| chr12:69496813
|
A | G | 1 | a0001c0001t0004g0106 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-261+26283A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496813 | ||||||
| chr12:69496851
|
A | T | 81 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(78): Show | 81 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.-261+26321A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69496851 | ||||||
| chr12:69497088
|
A | G | 1 | a0001c0001t0002g0326 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-261+26558A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69497088 | ||||||
| chr12:69497153
|
T | C | 1 | a0001c0002t0001g0135 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-261+26623T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69497153 | ||||||
| chr12:69497330
|
G | A | 92 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0013g0189others(89): Show | 92 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.-261+26800G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69497330 | ||||||
| chr12:69497465
|
G | C | 2 | a0001c0002t0001g0137a0001c0002t0001g0150 | 2 | NA18945.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-261+26935G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69497465 | ||||||
| chr12:69497551
|
C | A | 1 | a0001c0001t0004g0081 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-261+27021C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69497551 | ||||||
| chr12:69497573
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-261+27043C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69497573 | ||||||
| chr12:69497574
|
G | A | 2 | a0001c0001t0017g0302a0001c0001t0017g0303 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-261+27044G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69497574 | ||||||
| chr12:69497632
|
G | A | 233 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(230): Show | 234 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(231): Show |
intron_variant | MODIFIER | c.-261+27102G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69497632 | ||||||
| chr12:69497646
|
G | A | 1 | a0001c0001t0020g0224 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-261+27116G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69497646 | ||||||
| chr12:69497782
|
C | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+27252C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69497782 | ||||||
| chr12:69498018
|
AT | A | 117 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(114): Show | 118 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.-261+27498delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498018 | |||||
| chr12:69498018
|
ATT | A | 112 | a0001c0001t0001g0226a0001c0001t0003g0176a0001c0001t0003g0177others(109): Show | 112 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.-261+27497_-261+27 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498018 | |||||
| chr12:69498048
|
CAGT | C | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-261+27521_-261+27 others(9): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498048 | |||||
| chr12:69498120
|
G | T | 233 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(230): Show | 234 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(231): Show |
intron_variant | MODIFIER | c.-261+27590G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498120 | ||||||
| chr12:69498135
|
G | T | 1 | a0001c0001t0004g0081 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-261+27605G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498135 | ||||||
| chr12:69498327
|
A | T | 1 | a0001c0001t0004g0081 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-261+27797A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498327 | ||||||
| chr12:69498366
|
A | G | 13 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+27836A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498366 | ||||||
| chr12:69498444
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-261+27914G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498444 | ||||||
| chr12:69498460
|
G | A | 219 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(216): Show | 219 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(216): Show |
intron_variant | MODIFIER | c.-261+27930G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498460 | ||||||
| chr12:69498519
|
T | TGTGTGTG others(6): Show |
1 | a0001c0002t0001g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-261+27989_-261+27 others(19): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498519 | ||||||
| chr12:69498519
|
T | TGTGTGTG others(10): Show |
2 | a0001c0002t0001g0131a0001c0002t0001g0180 | 2 | HG01517.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-261+27989_-261+27 others(23): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498519 | ||||||
| chr12:69498519
|
T | TTG | 4 | a0001c0001t0003g0028a0001c0001t0003g0230a0001c0001t0028g0011others(1): Show | 5 | HG00544.hp1 HG02886.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.-261+28021_-261+28 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
T | TTGTG | 13 | a0001c0001t0023g0105a0001c0002t0001g0262a0001c0002t0006g0252others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-261+28019_-261+28 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
T | TTGTGTG | 3 | a0001c0001t0002g0203a0001c0001t0002g0315a0001c0002t0006g0261 | 3 | HG01106.hp2 NA19054.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-261+28017_-261+28 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
T | TTGTGTGT others(1): Show |
61 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0270others(58): Show | 61 | HG00558.hp1 HG00609.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.-261+28015_-261+28 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
T | TTGTGTGT others(3): Show |
26 | a0001c0001t0002g0273a0001c0001t0002g0281a0001c0001t0002g0282others(23): Show | 26 | HG00544.hp2 HG01346.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-261+28013_-261+28 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
T | TTGTGTGT others(5): Show |
30 | a0001c0001t0002g0269a0001c0001t0002g0280a0001c0001t0002g0310others(27): Show | 30 | HG00408.hp1 HG01358.hp1 HG01928.hp2 others(27): Show |
intron_variant | MODIFIER | c.-261+28011_-261+28 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
T | TTGTGTGT others(7): Show |
38 | a0001c0001t0002g0309a0001c0001t0008g0005a0001c0001t0008g0006others(35): Show | 38 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.-261+28009_-261+28 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
T | TTGTGTGT others(9): Show |
19 | a0001c0001t0002g0267a0001c0002t0001g0117a0001c0002t0001g0128others(16): Show | 19 | HG00099.hp2 HG00735.hp2 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.-261+28007_-261+28 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
T | TTGTGTGT others(11): Show |
9 | a0001c0002t0001g0110a0001c0002t0001g0122a0001c0002t0001g0132others(6): Show | 9 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+28005_-261+28 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
T | TTGTGTGT others(13): Show |
9 | a0001c0001t0001g0226a0001c0001t0002g0266a0001c0002t0001g0125others(6): Show | 9 | HG00741.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+28003_-261+28 others(26): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
T | TTGTGTGT others(15): Show |
1 | a0001c0002t0001g0193 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-261+28001_-261+28 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498519
|
TTG | T | 57 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(54): Show | 57 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.-261+28021_-261+28 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69498519 | |||||
| chr12:69498635
|
A | G | 2 | a0001c0001t0002g0289a0001c0001t0002g0321 | 2 | HG01934.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-261+28105A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498635 | ||||||
| chr12:69498746
|
G | C | 73 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(70): Show | 73 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-261+28216G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498746 | ||||||
| chr12:69498763
|
C | G | 5 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(2): Show | 5 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-261+28233C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498763 | ||||||
| chr12:69498768
|
C | T | 146 | a0001c0001t0001g0226a0001c0001t0003g0176a0001c0001t0003g0177others(143): Show | 146 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.-261+28238C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498768 | ||||||
| chr12:69498806
|
G | A | 1 | a0001c0002t0001g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-261+28276G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498806 | ||||||
| chr12:69498810
|
T | C | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-261+28280T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498810 | ||||||
| chr12:69498833
|
T | A | 1 | a0001c0001t0004g0081 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-261+28303T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498833 | ||||||
| chr12:69498944
|
T | G | 6 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-261+28414T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69498944 | ||||||
| chr12:69499007
|
T | G | 1 | a0001c0002t0001g0162 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-261+28477T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499007 | ||||||
| chr12:69499078
|
C | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+28548C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499078 | ||||||
| chr12:69499162
|
CTA | C | 73 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(70): Show | 73 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-261+28634_-261+28 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69499162 | |||||
| chr12:69499222
|
G | T | 1 | a0001c0001t0004g0081 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-261+28692G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499222 | ||||||
| chr12:69499223
|
G | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+28693G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499223 | ||||||
| chr12:69499238
|
G | A | 1 | a0001c0001t0008g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-261+28708G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499238 | ||||||
| chr12:69499284
|
A | G | 76 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(73): Show | 76 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.-261+28754A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499284 | ||||||
| chr12:69499391
|
A | T | 1 | a0001c0001t0004g0081 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-261+28861A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499391 | ||||||
| chr12:69499593
|
G | A | 115 | a0001c0001t0001g0226a0001c0001t0003g0176a0001c0001t0003g0177others(112): Show | 115 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.-261+29063G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499593 | ||||||
| chr12:69499755
|
G | T | 1 | a0001c0001t0004g0081 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-261+29225G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499755 | ||||||
| chr12:69499796
|
G | A | 1 | a0001c0001t0004g0098 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-261+29266G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499796 | ||||||
| chr12:69499805
|
G | A | 13 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-261+29275G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499805 | ||||||
| chr12:69499847
|
A | G | 1 | a0001c0002t0001g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-261+29317A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499847 | ||||||
| chr12:69499870
|
G | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-261+29340G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69499870 | ||||||
| chr12:69500029
|
G | A | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-261+29499G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69500029 | ||||||
| chr12:69500079
|
C | T | 9 | a0001c0001t0004g0078a0001c0001t0004g0079a0001c0001t0004g0080others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-261+29549C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69500079 | ||||||
| chr12:69500142
|
C | T | 73 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(70): Show | 73 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-261+29612C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69500142 | ||||||
| chr12:69500194
|
G | A | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-261+29664G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69500194 | ||||||
| chr12:69500244
|
G | A | 1 | a0001c0002t0007g0154 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-261+29714G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69500244 | ||||||
| chr12:69500736
|
T | C | 5 | a0001c0002t0007g0121a0001c0002t0007g0154a0001c0002t0007g0155others(2): Show | 5 | HG00741.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-260-30129T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69500736 | ||||||
| chr12:69500809
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-260-30056C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69500809 | ||||||
| chr12:69500837
|
A | T | 5 | a0001c0001t0002g0308a0001c0001t0002g0314a0001c0001t0002g0318others(2): Show | 5 | NA18971.hp1 NA18980.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.-260-30028A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69500837 | ||||||
| chr12:69500875
|
A | C | 1 | a0001c0001t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-260-29990A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69500875 | ||||||
| chr12:69500915
|
A | G | 4 | a0001c0001t0005g0240a0001c0001t0005g0243a0001c0001t0005g0244others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-29950A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69500915 | ||||||
| chr12:69501014
|
G | T | 3 | a0001c0001t0015g0153a0001c0002t0001g0149a0001c0002t0001g0179 | 3 | HG02683.hp1 HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-260-29851G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69501014 | ||||||
| chr12:69501172
|
TA | T | 232 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(229): Show | 233 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(230): Show |
intron_variant | MODIFIER | c.-260-29680delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69501172 | |||||
| chr12:69501258
|
A | G | 1 | a0001c0002t0001g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-260-29607A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69501258 | ||||||
| chr12:69501263
|
C | T | 1 | a0001c0002t0018g0136 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-260-29602C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69501263 | ||||||
| chr12:69501390
|
C | A | 1 | a0001c0002t0007g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-260-29475C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69501390 | ||||||
| chr12:69501632
|
A | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-29233A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69501632 | ||||||
| chr12:69501711
|
G | A | 2 | a0001c0001t0004g0090a0001c0001t0004g0209 | 2 | HG01516.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-260-29154G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69501711 | ||||||
| chr12:69501949
|
CTGTTTTT others(7): Show |
C | 90 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(87): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-260-28900_-260-28 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69501949 | |||||
| chr12:69501965
|
G | T | 77 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(74): Show | 77 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-260-28900G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69501965 | ||||||
| chr12:69502402
|
A | T | 5 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(2): Show | 5 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-28463A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69502402 | ||||||
| chr12:69502518
|
G | A | 112 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0009g0336others(109): Show | 112 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.-260-28347G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69502518 | ||||||
| chr12:69502522
|
C | T | 1 | a0001c0002t0001g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-260-28343C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69502522 | ||||||
| chr12:69502529
|
C | T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-28336C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69502529 | ||||||
| chr12:69502726
|
G | A | 3 | a0001c0001t0023g0105a0001c0002t0001g0172a0001c0002t0001g0220 | 3 | HG02055.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-260-28139G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69502726 | ||||||
| chr12:69502883
|
T | G | 1 | a0001c0002t0001g0117 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-260-27982T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69502883 | ||||||
| chr12:69503145
|
C | G | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-260-27720C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69503145 | ||||||
| chr12:69503847
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-27018C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69503847 | ||||||
| chr12:69503947
|
T | C | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-260-26918T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69503947 | ||||||
| chr12:69504070
|
A | G | 1 | a0001c0002t0006g0257 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-260-26795A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69504070 | ||||||
| chr12:69504077
|
T | G | 1 | a0001c0001t0026g0145 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-260-26788T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69504077 | ||||||
| chr12:69504127
|
C | G | 6 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-26738C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69504127 | ||||||
| chr12:69504250
|
A | G | 18 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(15): Show | 18 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-260-26615A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69504250 | ||||||
| chr12:69504486
|
T | C | 1 | a0001c0001t0002g0330 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-260-26379T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69504486 | ||||||
| chr12:69504524
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-260-26341A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69504524 | ||||||
| chr12:69504785
|
C | T | 1 | a0001c0001t0003g0072 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-260-26080C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69504785 | ||||||
| chr12:69504825
|
G | A | 1 | a0001c0002t0001g0108 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-260-26040G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69504825 | ||||||
| chr12:69505090
|
C | T | 108 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0013g0189others(105): Show | 108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-260-25775C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69505090 | ||||||
| chr12:69505318
|
G | A | 3 | a0001c0001t0003g0024a0001c0001t0003g0027a0001c0001t0034g0025 | 3 | HG02132.hp2 HG02523.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-260-25547G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69505318 | ||||||
| chr12:69505337
|
A | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-25528A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69505337 | ||||||
| chr12:69505556
|
G | T | 106 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0013g0189others(103): Show | 106 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-260-25309G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69505556 | ||||||
| chr12:69505623
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-25242C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69505623 | ||||||
| chr12:69505768
|
G | A | 1 | a0001c0001t0003g0051 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-260-25097G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69505768 | ||||||
| chr12:69505844
|
G | A | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-25021G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69505844 | ||||||
| chr12:69505956
|
T | C | 2 | a0001c0002t0001g0182a0001c0002t0001g0185 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-260-24909T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69505956 | ||||||
| chr12:69506028
|
C | G | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-24837C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69506028 | ||||||
| chr12:69506231
|
A | G | 1 | a0001c0001t0005g0250 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-260-24634A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69506231 | ||||||
| chr12:69506428
|
G | A | 220 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(217): Show | 220 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(217): Show |
intron_variant | MODIFIER | c.-260-24437G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69506428 | ||||||
| chr12:69506648
|
C | T | 1 | a0001c0002t0007g0121 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-260-24217C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69506648 | ||||||
| chr12:69506654
|
A | G | 5 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(2): Show | 5 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-24211A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69506654 | ||||||
| chr12:69506871
|
C | A | 1 | a0001c0001t0002g0321 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-260-23994C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69506871 | ||||||
| chr12:69506991
|
C | T | 233 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(230): Show | 234 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(231): Show |
intron_variant | MODIFIER | c.-260-23874C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69506991 | ||||||
| chr12:69507274
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-260-23591C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69507274 | ||||||
| chr12:69507354
|
AT | A | 3 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0002t0001g0183 | 3 | NA18991.hp1 NA19054.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-260-23510delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69507354 | ||||||
| chr12:69507452
|
G | A | 90 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(87): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-260-23413G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69507452 | ||||||
| chr12:69507559
|
T | G | 1 | a0001c0001t0010g0094 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-260-23306T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69507559 | ||||||
| chr12:69507765
|
C | T | 2 | a0001c0001t0017g0302a0001c0001t0017g0303 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-260-23100C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69507765 | ||||||
| chr12:69507788
|
G | C | 1 | a0001c0002t0001g0220 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-260-23077G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69507788 | ||||||
| chr12:69507796
|
G | A | 73 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(70): Show | 73 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-260-23069G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69507796 | ||||||
| chr12:69507831
|
C | T | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-260-23034C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69507831 | ||||||
| chr12:69507916
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-260-22949C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69507916 | ||||||
| chr12:69508019
|
C | T | 1 | a0001c0002t0001g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-260-22846C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508019 | ||||||
| chr12:69508024
|
C | CA | 24 | a0001c0001t0002g0205a0001c0001t0002g0280a0001c0001t0002g0281others(21): Show | 24 | HG00741.hp2 HG01934.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.-260-22811dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69508024 | |||||
| chr12:69508024
|
CA | C | 208 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0203others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.-260-22811delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69508024 | |||||
| chr12:69508024
|
CAA | C | 19 | a0001c0001t0001g0226a0001c0001t0002g0064a0001c0001t0002g0208others(16): Show | 19 | HG01169.hp1 HG02257.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.-260-22812_-260-22 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69508024 | |||||
| chr12:69508024
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0002t0001g0172a0001c0002t0001g0220 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-260-22820_-260-22 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69508024 | |||||
| chr12:69508055
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-260-22810G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508055 | ||||||
| chr12:69508056
|
T | A | 1 | a0001c0001t0002g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-260-22809T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508056 | ||||||
| chr12:69508057
|
T | A | 1 | a0001c0001t0002g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-260-22808T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508057 | ||||||
| chr12:69508064
|
G | T | 1 | a0001c0001t0002g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-260-22801G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508064 | ||||||
| chr12:69508111
|
T | G | 1 | a0001c0001t0005g0240 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-260-22754T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508111 | ||||||
| chr12:69508174
|
C | A | 4 | a0001c0002t0001g0159a0001c0002t0001g0164a0001c0002t0001g0182others(1): Show | 4 | HG01346.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-22691C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508174 | ||||||
| chr12:69508294
|
T | C | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-260-22571T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508294 | ||||||
| chr12:69508406
|
A | G | 91 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(88): Show | 91 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-260-22459A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508406 | ||||||
| chr12:69508466
|
A | G | 1 | a0001c0001t0004g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-260-22399A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508466 | ||||||
| chr12:69508708
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-260-22157G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508708 | ||||||
| chr12:69508844
|
C | G | 1 | a0001c0001t0003g0040 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-260-22021C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508844 | ||||||
| chr12:69508858
|
T | A | 1 | a0001c0001t0003g0020 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-260-22007T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508858 | ||||||
| chr12:69508905
|
G | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-21960G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69508905 | ||||||
| chr12:69509301
|
G | C | 1 | a0001c0001t0030g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-260-21564G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69509301 | ||||||
| chr12:69509335
|
A | G | 66 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(63): Show | 66 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-260-21530A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69509335 | ||||||
| chr12:69509412
|
T | A | 1 | a0001c0002t0006g0263 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-260-21453T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69509412 | ||||||
| chr12:69509413
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-260-21452G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69509413 | ||||||
| chr12:69509539
|
C | T | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-260-21326C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69509539 | ||||||
| chr12:69509632
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-21233A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69509632 | ||||||
| chr12:69509775
|
C | A | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-21090C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69509775 | ||||||
| chr12:69509835
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-21030C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69509835 | ||||||
| chr12:69509960
|
C | A | 1 | a0001c0001t0004g0084 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-260-20905C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69509960 | ||||||
| chr12:69510061
|
A | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-20804A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69510061 | ||||||
| chr12:69510214
|
T | C | 1 | a0001c0001t0005g0240 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-260-20651T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69510214 | ||||||
| chr12:69510289
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-260-20576C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69510289 | ||||||
| chr12:69510357
|
G | A | 1 | a0001c0001t0014g0009 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-260-20508G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69510357 | ||||||
| chr12:69510374
|
A | G | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-260-20491A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69510374 | ||||||
| chr12:69510571
|
T | C | 118 | a0001c0001t0001g0226a0001c0001t0003g0176a0001c0001t0003g0177others(115): Show | 118 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-260-20294T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69510571 | ||||||
| chr12:69510646
|
G | C | 1 | a0001c0001t0003g0228 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-260-20219G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69510646 | ||||||
| chr12:69510794
|
A | G | 4 | a0001c0002t0001g0117a0001c0002t0001g0118a0001c0002t0001g0194others(1): Show | 4 | HG01361.hp1 HG02135.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-20071A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69510794 | ||||||
| chr12:69510974
|
A | G | 1 | a0001c0001t0005g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-260-19891A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69510974 | ||||||
| chr12:69511182
|
T | C | 73 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(70): Show | 73 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-260-19683T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69511182 | ||||||
| chr12:69511241
|
C | A | 5 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(2): Show | 5 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-19624C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69511241 | ||||||
| chr12:69511349
|
A | G | 44 | a0001c0001t0003g0016a0001c0001t0003g0033a0001c0001t0003g0034others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-260-19516A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69511349 | ||||||
| chr12:69511688
|
G | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-19177G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69511688 | ||||||
| chr12:69511757
|
G | A | 13 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-260-19108G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69511757 | ||||||
| chr12:69511810
|
G | T | 2 | a0001c0001t0003g0039a0001c0001t0003g0048 | 2 | HG02074.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-260-19055G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69511810 | ||||||
| chr12:69511835
|
A | G | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-19030A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69511835 | ||||||
| chr12:69511960
|
G | A | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-260-18905G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69511960 | ||||||
| chr12:69512239
|
G | A | 1 | a0001c0001t0002g0277 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-260-18626G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69512239 | ||||||
| chr12:69512386
|
A | G | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-260-18479A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69512386 | ||||||
| chr12:69512507
|
A | G | 80 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(77): Show | 80 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-260-18358A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69512507 | ||||||
| chr12:69512720
|
G | A | 13 | a0001c0001t0003g0016a0001c0001t0003g0036a0001c0001t0003g0039others(10): Show | 13 | HG00408.hp2 HG02040.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-18145G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69512720 | ||||||
| chr12:69512740
|
G | C | 308 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(305): Show | 309 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.-260-18125G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69512740 | ||||||
| chr12:69512762
|
T | C | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-260-18103T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69512762 | ||||||
| chr12:69512831
|
C | T | 1 | a0001c0002t0011g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-260-18034C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69512831 | ||||||
| chr12:69512978
|
C | T | 7 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-260-17887C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69512978 | ||||||
| chr12:69513115
|
CT | C | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-260-17749delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513115 | ||||||
| chr12:69513116
|
T | C | 238 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(235): Show | 239 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(236): Show |
intron_variant | MODIFIER | c.-260-17749T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513116 | ||||||
| chr12:69513125
|
C | G | 80 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(77): Show | 80 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-260-17740C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513125 | ||||||
| chr12:69513146
|
A | G | 308 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(305): Show | 309 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.-260-17719A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513146 | ||||||
| chr12:69513151
|
G | GT | 250 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(247): Show | 250 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-260-17702dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69513151 | |||||
| chr12:69513151
|
G | GTT | 13 | a0001c0002t0001g0108a0001c0002t0001g0124a0001c0002t0001g0134others(10): Show | 13 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.-260-17703_-260-17 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69513151 | |||||
| chr12:69513151
|
GT | G | 11 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(8): Show | 11 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-260-17702delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69513151 | |||||
| chr12:69513152
|
T | C | 5 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(2): Show | 5 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-17713T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513152 | ||||||
| chr12:69513154
|
T | TG | 8 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(5): Show | 8 | NA18951.hp1 NA18955.hp1 NA18995.hp2 others(5): Show |
intron_variant | MODIFIER | c.-260-17711_-260-17 others(7): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513154 | ||||||
| chr12:69513155
|
T | G | 7 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(4): Show | 7 | NA18951.hp1 NA18995.hp2 NA19060.hp2 others(4): Show |
intron_variant | MODIFIER | c.-260-17710T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513155 | ||||||
| chr12:69513195
|
A | G | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-17670A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513195 | ||||||
| chr12:69513292
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-17573A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513292 | ||||||
| chr12:69513453
|
A | G | 1 | a0001c0001t0008g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-260-17412A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513453 | ||||||
| chr12:69513524
|
A | G | 1 | a0001c0001t0015g0153 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-260-17341A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513524 | ||||||
| chr12:69513625
|
G | C | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-260-17240G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513625 | ||||||
| chr12:69513713
|
A | T | 1 | a0001c0001t0008g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-260-17152A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513713 | ||||||
| chr12:69513822
|
A | G | 70 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.-260-17043A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513822 | ||||||
| chr12:69513914
|
T | C | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-260-16951T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513914 | ||||||
| chr12:69513940
|
G | A | 3 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0001g0193 | 3 | NA18954.hp2 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-260-16925G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513940 | ||||||
| chr12:69513949
|
T | G | 1 | a0001c0002t0001g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-260-16916T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513949 | ||||||
| chr12:69514369
|
C | T | 224 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(221): Show | 225 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.-260-16496C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69514369 | ||||||
| chr12:69514584
|
G | C | 2 | a0001c0002t0001g0160a0001c0002t0001g0181 | 2 | HG01123.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-260-16281G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69514584 | ||||||
| chr12:69514590
|
T | C | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-260-16275T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69514590 | ||||||
| chr12:69514649
|
A | C | 91 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(88): Show | 91 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-260-16216A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69514649 | ||||||
| chr12:69514654
|
G | A | 1 | a0001c0001t0005g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-260-16211G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69514654 | ||||||
| chr12:69514765
|
G | A | 73 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(70): Show | 73 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-260-16100G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69514765 | ||||||
| chr12:69514831
|
CA | C | 301 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(298): Show | 302 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.-260-16021delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69514831 | |||||
| chr12:69514885
|
T | A | 1 | a0001c0001t0031g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-260-15980T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69514885 | ||||||
| chr12:69514954
|
C | T | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-260-15911C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69514954 | ||||||
| chr12:69515121
|
A | G | 1 | a0001c0002t0001g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-260-15744A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69515121 | ||||||
| chr12:69515530
|
A | C | 1 | a0001c0001t0003g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-260-15335A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69515530 | ||||||
| chr12:69515561
|
G | A | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-15304G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69515561 | ||||||
| chr12:69515562
|
C | T | 6 | a0001c0001t0002g0308a0001c0001t0002g0314a0001c0001t0002g0318others(3): Show | 6 | HG02027.hp1 NA18971.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-15303C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69515562 | ||||||
| chr12:69515591
|
A | G | 1 | a0001c0001t0030g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-260-15274A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69515591 | ||||||
| chr12:69515600
|
T | C | 243 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(240): Show | 244 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(241): Show |
intron_variant | MODIFIER | c.-260-15265T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69515600 | ||||||
| chr12:69515769
|
C | CT | 11 | a0001c0001t0003g0039a0001c0001t0008g0002a0001c0001t0008g0003others(8): Show | 11 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-260-15081dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69515769 | |||||
| chr12:69515769
|
CT | C | 27 | a0001c0001t0002g0271a0001c0001t0002g0276a0001c0001t0002g0291others(24): Show | 27 | HG01069.hp1 HG01109.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.-260-15081delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69515769 | |||||
| chr12:69515830
|
CCTCT | C | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-260-15032_-260-15 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69515830 | |||||
| chr12:69516008
|
A | G | 1 | a0001c0001t0004g0082 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-260-14857A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516008 | ||||||
| chr12:69516026
|
A | G | 1 | a0001c0001t0003g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-260-14839A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516026 | ||||||
| chr12:69516221
|
A | AT | 29 | a0001c0001t0004g0078a0001c0001t0004g0079a0001c0001t0004g0080others(26): Show | 29 | HG00408.hp1 HG00733.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.-260-14630dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69516221 | |||||
| chr12:69516221
|
AT | A | 31 | a0001c0001t0002g0326a0001c0001t0005g0239a0001c0001t0005g0240others(28): Show | 32 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-260-14630delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69516221 | |||||
| chr12:69516279
|
C | T | 4 | a0001c0002t0012g0083a0001c0002t0012g0086a0001c0002t0012g0099others(1): Show | 4 | HG01192.hp1 HG01934.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-14586C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516279 | ||||||
| chr12:69516364
|
G | A | 1 | a0001c0002t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-260-14501G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516364 | ||||||
| chr12:69516377
|
C | T | 17 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(14): Show | 17 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-260-14488C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516377 | ||||||
| chr12:69516484
|
C | T | 89 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191others(86): Show | 89 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-260-14381C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516484 | ||||||
| chr12:69516683
|
T | C | 1 | a0001c0002t0001g0262 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-260-14182T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516683 | ||||||
| chr12:69516705
|
T | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-14160T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516705 | ||||||
| chr12:69516749
|
T | C | 1 | a0001c0002t0018g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-260-14116T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516749 | ||||||
| chr12:69516830
|
A | G | 1 | a0001c0002t0001g0200 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-260-14035A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516830 | ||||||
| chr12:69516861
|
T | C | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-260-14004T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69516861 | ||||||
| chr12:69517043
|
TG | T | 4 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-13819delG | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69517043 | |||||
| chr12:69517071
|
A | G | 73 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(70): Show | 73 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-260-13794A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517071 | ||||||
| chr12:69517195
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-13670C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517195 | ||||||
| chr12:69517230
|
A | G | 1 | a0001c0001t0034g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-260-13635A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517230 | ||||||
| chr12:69517256
|
G | A | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-260-13609G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517256 | ||||||
| chr12:69517457
|
A | G | 98 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(95): Show | 98 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-260-13408A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517457 | ||||||
| chr12:69517639
|
TA | T | 103 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191others(100): Show | 103 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.-260-13225delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517639 | ||||||
| chr12:69517643
|
C | G | 2 | a0001c0001t0005g0244a0001c0001t0033g0242 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-260-13222C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517643 | ||||||
| chr12:69517705
|
C | T | 1 | a0001c0001t0002g0322 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-260-13160C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517705 | ||||||
| chr12:69517775
|
G | A | 2 | a0001c0002t0001g0172a0001c0002t0001g0220 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-260-13090G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517775 | ||||||
| chr12:69517891
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | HG03041.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-260-12974C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517891 | ||||||
| chr12:69517924
|
A | G | 2 | a0001c0002t0001g0216a0001c0002t0001g0251 | 2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-260-12941A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517924 | ||||||
| chr12:69517927
|
T | G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | HG03041.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-260-12938T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517927 | ||||||
| chr12:69518027
|
G | A | 1 | a0001c0002t0001g0200 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-260-12838G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69518027 | ||||||
| chr12:69518262
|
C | A | 1 | a0001c0001t0003g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-260-12603C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69518262 | ||||||
| chr12:69518270
|
T | C | 102 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.-260-12595T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69518270 | ||||||
| chr12:69518327
|
C | G | 230 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(227): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.-260-12538C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69518327 | ||||||
| chr12:69518402
|
AT | A | 229 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(226): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.-260-12451delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69518402 | |||||
| chr12:69518542
|
G | A | 1 | a0001c0001t0031g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-260-12323G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69518542 | ||||||
| chr12:69518597
|
C | T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-12268C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69518597 | ||||||
| chr12:69518713
|
TAAAA | T | 46 | a0001c0001t0003g0016a0001c0001t0003g0033a0001c0001t0003g0034others(43): Show | 46 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.-260-12142_-260-12 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69518713 | |||||
| chr12:69518744
|
G | GTGGCTCA others(10): Show |
1 | a0001c0002t0001g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-260-12120_-260-12 others(23): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69518744 | |||||
| chr12:69518748
|
C | T | 1 | a0001c0001t0003g0041 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-260-12117C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69518748 | ||||||
| chr12:69518894
|
A | G | 110 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(107): Show | 110 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-260-11971A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69518894 | ||||||
| chr12:69518982
|
A | G | 32 | a0001c0001t0004g0077a0001c0001t0004g0078a0001c0001t0004g0079others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.-260-11883A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69518982 | ||||||
| chr12:69518996
|
C | CA | 74 | a0001c0001t0002g0208a0001c0001t0003g0016a0001c0001t0003g0017others(71): Show | 74 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.-260-11850dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69518996 | |||||
| chr12:69518996
|
CA | C | 35 | a0001c0001t0002g0204a0001c0001t0002g0275a0001c0001t0002g0290others(32): Show | 36 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.-260-11850delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69518996 | |||||
| chr12:69519026
|
G | A | 2 | a0001c0001t0009g0340a0001c0001t0009g0341 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-260-11839G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519026 | ||||||
| chr12:69519103
|
T | G | 1 | a0001c0002t0001g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-260-11762T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519103 | ||||||
| chr12:69519436
|
G | A | 1 | a0001c0002t0001g0169 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-260-11429G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519436 | ||||||
| chr12:69519559
|
C | T | 5 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(2): Show | 5 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-11306C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519559 | ||||||
| chr12:69519580
|
A | G | 1 | a0001c0002t0001g0172 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-260-11285A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519580 | ||||||
| chr12:69519593
|
G | GT | 71 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-260-11270dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69519593 | |||||
| chr12:69519601
|
CTT | C | 109 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(106): Show | 109 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-260-11262_-260-11 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69519601 | |||||
| chr12:69519610
|
C | A | 1 | a0001c0002t0001g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-260-11255C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519610 | ||||||
| chr12:69519611
|
A | T | 1 | a0001c0002t0001g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-260-11254A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519611 | ||||||
| chr12:69519612
|
T | G | 1 | a0001c0002t0001g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-260-11253T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519612 | ||||||
| chr12:69519676
|
G | C | 1 | a0001c0002t0024g0219 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-260-11189G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519676 | ||||||
| chr12:69519721
|
G | A | 103 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191others(100): Show | 103 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.-260-11144G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519721 | ||||||
| chr12:69519733
|
A | C | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-11132A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519733 | ||||||
| chr12:69519748
|
T | C | 1 | a0001c0001t0023g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-260-11117T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519748 | ||||||
| chr12:69519800
|
A | T | 1 | a0001c0001t0002g0271 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-260-11065A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69519800 | ||||||
| chr12:69520085
|
T | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-10780T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520085 | ||||||
| chr12:69520195
|
G | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-10670G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520195 | ||||||
| chr12:69520211
|
GA | G | 31 | a0001c0001t0003g0016a0001c0001t0003g0033a0001c0001t0003g0034others(28): Show | 31 | HG00408.hp2 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-260-10650delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69520211 | |||||
| chr12:69520330
|
G | A | 238 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(235): Show | 239 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(236): Show |
intron_variant | MODIFIER | c.-260-10535G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520330 | ||||||
| chr12:69520367
|
CTATTA | C | 13 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-260-10496_-260-10 others(11): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69520367 | |||||
| chr12:69520376
|
G | GT | 23 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0271others(20): Show | 23 | HG00609.hp2 HG01358.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.-260-10470dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69520376 | |||||
| chr12:69520376
|
G | GTT | 13 | a0001c0001t0008g0003a0001c0002t0001g0262a0001c0002t0006g0001others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-260-10471_-260-10 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69520376 | |||||
| chr12:69520376
|
GT | G | 119 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(116): Show | 119 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.-260-10470delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69520376 | |||||
| chr12:69520376
|
GTT | G | 14 | a0001c0002t0001g0108a0001c0002t0001g0124a0001c0002t0001g0134others(11): Show | 14 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.-260-10471_-260-10 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69520376 | |||||
| chr12:69520534
|
G | A | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-10331G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520534 | ||||||
| chr12:69520655
|
C | A | 3 | a0001c0001t0002g0273a0001c0001t0002g0301a0001c0001t0002g0333 | 3 | NA18984.hp2 NA18988.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-260-10210C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520655 | ||||||
| chr12:69520738
|
G | A | 104 | a0001c0001t0002g0299a0001c0001t0013g0189a0001c0001t0013g0190others(101): Show | 104 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-260-10127G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520738 | ||||||
| chr12:69520765
|
A | G | 1 | a0001c0001t0008g0006 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-260-10100A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520765 | ||||||
| chr12:69520839
|
T | C | 1 | a0001c0002t0001g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-260-10026T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520839 | ||||||
| chr12:69520846
|
G | A | 4 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0102others(1): Show | 4 | NA18971.hp2 NA18998.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-260-10019G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520846 | ||||||
| chr12:69520848
|
A | G | 73 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(70): Show | 73 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-260-10017A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520848 | ||||||
| chr12:69520936
|
A | T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-9929A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520936 | ||||||
| chr12:69520937
|
T | A | 4 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010others(1): Show | 4 | HG01167.hp2 HG01361.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-9928T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69520937 | ||||||
| chr12:69521034
|
G | A | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-260-9831G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521034 | ||||||
| chr12:69521151
|
T | G | 78 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(75): Show | 78 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.-260-9714T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521151 | ||||||
| chr12:69521276
|
G | GT | 3 | a0001c0002t0007g0113a0001c0002t0007g0119a0001c0002t0007g0211 | 3 | HG02257.hp1 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-260-9586dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69521276 | |||||
| chr12:69521544
|
A | T | 5 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(2): Show | 5 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-9321A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521544 | ||||||
| chr12:69521646
|
C | T | 1 | a0001c0002t0012g0083 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-260-9219C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521646 | ||||||
| chr12:69521769
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-260-9096C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521769 | ||||||
| chr12:69521805
|
G | A | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-260-9060G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521805 | ||||||
| chr12:69521894
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-260-8971G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521894 | ||||||
| chr12:69521903
|
C | T | 1 | a0001c0001t0003g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-260-8962C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521903 | ||||||
| chr12:69521905
|
C | A | 4 | a0001c0002t0001g0159a0001c0002t0001g0164a0001c0002t0001g0182others(1): Show | 4 | HG01346.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-260-8960C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521905 | ||||||
| chr12:69521919
|
G | C | 1 | a0001c0002t0001g0156 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-260-8946G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521919 | ||||||
| chr12:69521940
|
G | A | 1 | a0001c0001t0002g0334 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-260-8925G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521940 | ||||||
| chr12:69521969
|
C | T | 111 | a0001c0001t0002g0299a0001c0001t0009g0336a0001c0001t0009g0337others(108): Show | 111 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-260-8896C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69521969 | ||||||
| chr12:69522190
|
T | TTG | 73 | a0001c0001t0002g0060a0001c0001t0002g0064a0001c0001t0002g0203others(70): Show | 73 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-260-8629_-260-862 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
T | TTGTG | 28 | a0001c0001t0001g0226a0001c0001t0002g0316a0001c0001t0003g0038others(25): Show | 28 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.-260-8631_-260-862 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
T | TTGTGTG | 15 | a0001c0001t0002g0061a0001c0001t0002g0204a0001c0001t0002g0305others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-8633_-260-862 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
T | TTGTGTGT others(1): Show |
6 | a0001c0001t0003g0075a0001c0001t0004g0087a0001c0001t0004g0097others(3): Show | 6 | HG00733.hp1 HG01928.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.-260-8635_-260-862 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0004g0091a0001c0001t0004g0096 | 2 | HG01496.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-260-8637_-260-862 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
TTG | T | 39 | a0001c0001t0002g0307a0001c0001t0003g0017a0001c0001t0003g0020others(36): Show | 39 | HG00408.hp1 HG00673.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.-260-8629_-260-862 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
TTGTG | T | 24 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0271others(21): Show | 24 | HG00733.hp2 HG00735.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-260-8631_-260-862 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0005g0239a0001c0001t0005g0241a0001c0002t0007g0113 | 3 | HG02257.hp1 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-260-8635_-260-862 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
TTGTGTGT others(3): Show |
T | 10 | a0001c0001t0005g0240a0001c0001t0005g0243a0001c0001t0005g0244others(7): Show | 10 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-260-8637_-260-862 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
TTGTGTGT others(5): Show |
T | 3 | a0001c0001t0002g0270a0001c0002t0001g0120a0001c0002t0001g0128 | 3 | HG03579.hp2 NA18985.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-260-8639_-260-862 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
TTGTGTGT others(7): Show |
T | 15 | a0001c0001t0002g0281a0001c0002t0001g0262a0001c0002t0006g0001others(12): Show | 16 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-260-8641_-260-862 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522190
|
TTGTGTGT others(9): Show |
T | 2 | a0001c0001t0002g0280a0001c0001t0002g0282 | 2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-260-8643_-260-862 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522190 | |||||
| chr12:69522297
|
CCCT | C | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-8560_-260-855 others(7): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69522297 | |||||
| chr12:69522534
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-8331C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69522534 | ||||||
| chr12:69522713
|
T | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-8152T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69522713 | ||||||
| chr12:69522743
|
T | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-260-8122T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69522743 | ||||||
| chr12:69522754
|
C | T | 7 | a0001c0001t0008g0003a0001c0001t0008g0004a0001c0001t0008g0005others(4): Show | 7 | HG02559.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-260-8111C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69522754 | ||||||
| chr12:69522813
|
A | G | 2 | a0001c0002t0001g0160a0001c0002t0001g0181 | 2 | HG01123.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-260-8052A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69522813 | ||||||
| chr12:69522920
|
A | G | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-260-7945A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69522920 | ||||||
| chr12:69523022
|
A | G | 1 | a0001c0001t0023g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-260-7843A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523022 | ||||||
| chr12:69523029
|
G | A | 65 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(62): Show | 65 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.-260-7836G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523029 | ||||||
| chr12:69523036
|
G | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-7829G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523036 | ||||||
| chr12:69523107
|
T | G | 5 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(2): Show | 5 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-260-7758T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523107 | ||||||
| chr12:69523158
|
G | A | 105 | a0001c0001t0001g0226a0001c0001t0002g0299a0001c0001t0013g0189others(102): Show | 105 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.-260-7707G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523158 | ||||||
| chr12:69523279
|
G | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-7586G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523279 | ||||||
| chr12:69523280
|
G | C | 1 | a0001c0002t0001g0139 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-260-7585G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523280 | ||||||
| chr12:69523339
|
C | G | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-260-7526C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523339 | ||||||
| chr12:69523351
|
GA | G | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-260-7513delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523351 | ||||||
| chr12:69523402
|
T | A | 65 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(62): Show | 65 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.-260-7463T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523402 | ||||||
| chr12:69523482
|
A | G | 3 | a0001c0001t0005g0015a0001c0001t0025g0013a0001c0001t0031g0014 | 3 | HG01361.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-260-7383A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523482 | ||||||
| chr12:69523833
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-260-7032C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523833 | ||||||
| chr12:69523953
|
G | A | 1 | a0001c0001t0005g0240 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-260-6912G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69523953 | ||||||
| chr12:69524033
|
T | C | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-260-6832T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524033 | ||||||
| chr12:69524036
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-6829A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524036 | ||||||
| chr12:69524049
|
C | G | 1 | a0001c0002t0001g0194 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-260-6816C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524049 | ||||||
| chr12:69524069
|
G | A | 1 | a0001c0001t0008g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-260-6796G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524069 | ||||||
| chr12:69524099
|
G | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-6766G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524099 | ||||||
| chr12:69524131
|
C | G | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-260-6734C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524131 | ||||||
| chr12:69524153
|
G | A | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-260-6712G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524153 | ||||||
| chr12:69524157
|
G | T | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-260-6708G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524157 | ||||||
| chr12:69524286
|
C | T | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-260-6579C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524286 | ||||||
| chr12:69524367
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-6498C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524367 | ||||||
| chr12:69524390
|
G | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-6475G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524390 | ||||||
| chr12:69524487
|
G | A | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-6378G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524487 | ||||||
| chr12:69524572
|
T | C | 1 | a0001c0001t0005g0243 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-260-6293T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524572 | ||||||
| chr12:69524970
|
C | T | 3 | a0001c0002t0001g0140a0001c0002t0001g0178a0001c0002t0001g0214 | 3 | NA18953.hp2 NA19003.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-260-5895C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69524970 | ||||||
| chr12:69525092
|
T | G | 80 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(77): Show | 80 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-260-5773T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69525092 | ||||||
| chr12:69525141
|
A | C | 1 | a0001c0001t0002g0316 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-260-5724A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69525141 | ||||||
| chr12:69525167
|
A | T | 1 | a0001c0002t0001g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-260-5698A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69525167 | ||||||
| chr12:69525187
|
A | T | 1 | a0001c0002t0001g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-260-5678A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69525187 | ||||||
| chr12:69525192
|
GT | G | 293 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(290): Show | 294 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.-260-5659delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69525192 | |||||
| chr12:69525192
|
GTT | G | 9 | a0001c0001t0003g0034a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01346.hp1 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-260-5660_-260-565 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69525192 | |||||
| chr12:69525196
|
T | G | 1 | a0002c0004t0011g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-260-5669T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69525196 | ||||||
| chr12:69525319
|
A | G | 2 | a0001c0002t0001g0123a0001c0002t0001g0125 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-260-5546A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69525319 | ||||||
| chr12:69525633
|
C | T | 1 | a0001c0002t0001g0151 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-260-5232C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69525633 | ||||||
| chr12:69525678
|
C | T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-5187C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69525678 | ||||||
| chr12:69525729
|
A | G | 2 | a0001c0002t0001g0172a0001c0002t0001g0220 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-260-5136A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69525729 | ||||||
| chr12:69525807
|
G | A | 2 | a0001c0002t0001g0172a0001c0002t0001g0220 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-260-5058G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69525807 | ||||||
| chr12:69525841
|
CTTTA | C | 109 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(106): Show | 109 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-260-5016_-260-501 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69525841 | |||||
| chr12:69526021
|
G | A | 1 | a0001c0002t0001g0199 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-260-4844G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526021 | ||||||
| chr12:69526047
|
C | T | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-260-4818C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526047 | ||||||
| chr12:69526095
|
G | C | 2 | a0001c0002t0001g0172a0001c0002t0001g0220 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-260-4770G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526095 | ||||||
| chr12:69526386
|
T | C | 1 | a0001c0001t0002g0298 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-260-4479T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526386 | ||||||
| chr12:69526476
|
TTAA | T | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-260-4387_-260-438 others(7): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69526476 | |||||
| chr12:69526512
|
G | A | 1 | a0001c0002t0001g0186 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-260-4353G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526512 | ||||||
| chr12:69526664
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-260-4201A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526664 | ||||||
| chr12:69526759
|
C | T | 5 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-260-4106C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526759 | ||||||
| chr12:69526784
|
C | T | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-4081C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526784 | ||||||
| chr12:69526826
|
T | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-4039T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526826 | ||||||
| chr12:69526831
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-260-4034C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526831 | ||||||
| chr12:69526940
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-260-3925G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526940 | ||||||
| chr12:69526958
|
C | T | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-3907C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526958 | ||||||
| chr12:69526991
|
A | G | 1 | a0001c0002t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-260-3874A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69526991 | ||||||
| chr12:69527109
|
A | G | 2 | a0001c0001t0020g0224a0001c0001t0020g0225 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-260-3756A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527109 | ||||||
| chr12:69527163
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-260-3702C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527163 | ||||||
| chr12:69527205
|
A | G | 1 | a0001c0002t0001g0200 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-260-3660A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527205 | ||||||
| chr12:69527289
|
C | T | 1 | a0001c0001t0002g0203 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-260-3576C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527289 | ||||||
| chr12:69527325
|
G | GT | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-260-3527dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527325 | |||||
| chr12:69527325
|
GT | G | 67 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(64): Show | 67 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-260-3527delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527325 | |||||
| chr12:69527327
|
T | G | 1 | a0001c0002t0001g0265 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-260-3538T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527327 | ||||||
| chr12:69527338
|
T | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-3527T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527338 | ||||||
| chr12:69527343
|
A | ATTT | 10 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(7): Show | 10 | HG01109.hp2 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-260-3503_-260-350 others(7): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527343 | |||||
| chr12:69527343
|
A | ATTTTT | 7 | a0001c0001t0013g0189a0001c0001t0025g0013a0001c0002t0001g0120others(4): Show | 7 | HG01169.hp1 HG01361.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-260-3505_-260-350 others(9): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527343 | |||||
| chr12:69527343
|
A | ATTTTTT | 103 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0287others(100): Show | 103 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-260-3506_-260-350 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527343 | |||||
| chr12:69527343
|
A | ATTTTTTT | 70 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(67): Show | 71 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.-260-3507_-260-350 others(11): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527343 | |||||
| chr12:69527343
|
A | ATTTTTTT others(1): Show |
23 | a0001c0001t0002g0275a0001c0001t0002g0278a0001c0001t0002g0290others(20): Show | 23 | HG00558.hp1 HG00609.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-260-3508_-260-350 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527343 | |||||
| chr12:69527343
|
A | ATTTTTTT others(2): Show |
14 | a0001c0001t0002g0064a0001c0001t0002g0271a0001c0001t0002g0277others(11): Show | 14 | HG02451.hp2 HG02486.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.-260-3509_-260-350 others(13): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527343 | |||||
| chr12:69527343
|
A | ATTTTTTT others(3): Show |
31 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0003g0027others(28): Show | 31 | HG00408.hp2 HG00733.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.-260-3510_-260-350 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527343 | |||||
| chr12:69527343
|
A | ATTTTTTT others(4): Show |
23 | a0001c0001t0002g0208a0001c0001t0003g0017a0001c0001t0003g0019others(20): Show | 23 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.-260-3511_-260-350 others(15): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527343 | |||||
| chr12:69527343
|
A | ATTTTTTT others(5): Show |
7 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0003g0021others(4): Show | 7 | HG00673.hp2 HG01891.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.-260-3512_-260-350 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527343 | |||||
| chr12:69527343
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0003g0037 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-260-3513_-260-350 others(17): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69527343 | |||||
| chr12:69527365
|
A | T | 1 | a0001c0001t0004g0100 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-260-3500A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527365 | ||||||
| chr12:69527380
|
A | G | 1 | a0001c0002t0001g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-260-3485A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527380 | ||||||
| chr12:69527451
|
T | A | 1 | a0001c0001t0002g0330 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-260-3414T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527451 | ||||||
| chr12:69527582
|
A | T | 110 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(107): Show | 110 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-260-3283A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527582 | ||||||
| chr12:69527628
|
A | G | 78 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(75): Show | 78 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-260-3237A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527628 | ||||||
| chr12:69527719
|
A | G | 1 | a0001c0002t0001g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-260-3146A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527719 | ||||||
| chr12:69527829
|
T | C | 3 | a0001c0002t0007g0113a0001c0002t0007g0119a0001c0002t0007g0211 | 3 | HG02257.hp1 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-260-3036T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527829 | ||||||
| chr12:69527838
|
C | G | 2 | a0001c0001t0017g0302a0001c0001t0017g0303 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-260-3027C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527838 | ||||||
| chr12:69527853
|
A | G | 1 | a0001c0002t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-260-3012A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69527853 | ||||||
| chr12:69528000
|
GA | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-2864delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69528000 | ||||||
| chr12:69528186
|
T | A | 1 | a0001c0001t0002g0272 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-260-2679T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69528186 | ||||||
| chr12:69528309
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-260-2556G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69528309 | ||||||
| chr12:69528348
|
T | G | 1 | a0001c0001t0003g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-260-2517T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69528348 | ||||||
| chr12:69528731
|
A | G | 1 | a0001c0002t0006g0261 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-260-2134A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69528731 | ||||||
| chr12:69528854
|
A | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-2011A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69528854 | ||||||
| chr12:69528864
|
A | C | 1 | a0001c0001t0003g0032 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-260-2001A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69528864 | ||||||
| chr12:69528930
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-260-1935A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69528930 | ||||||
| chr12:69528958
|
A | G | 90 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(87): Show | 91 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-260-1907A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69528958 | ||||||
| chr12:69529057
|
C | T | 306 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(303): Show | 307 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.-260-1808C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69529057 | ||||||
| chr12:69529185
|
T | C | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-260-1680T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69529185 | ||||||
| chr12:69529359
|
C | T | 1 | a0001c0001t0002g0288 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-260-1506C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69529359 | ||||||
| chr12:69529442
|
G | A | 11 | a0001c0001t0002g0278a0001c0001t0002g0279a0001c0001t0002g0284others(8): Show | 11 | HG00597.hp2 NA18960.hp2 NA18961.hp1 others(8): Show |
intron_variant | MODIFIER | c.-260-1423G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69529442 | ||||||
| chr12:69529539
|
T | TGAACCTG others(4): Show |
2 | a0001c0002t0001g0172a0001c0002t0001g0220 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-260-1324_-260-131 others(15): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69529539 | |||||
| chr12:69529583
|
A | G | 66 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(63): Show | 66 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-260-1282A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69529583 | ||||||
| chr12:69529622
|
A | AAAAT | 10 | a0001c0001t0002g0267a0001c0001t0002g0280a0001c0001t0002g0281others(7): Show | 10 | HG02027.hp1 HG02273.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-260-1217_-260-121 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69529622 | |||||
| chr12:69529622
|
A | AAAATAAA others(5): Show |
3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-260-1225_-260-121 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69529622 | |||||
| chr12:69529622
|
AAAAT | A | 221 | a0001c0001t0001g0226a0001c0001t0003g0016a0001c0001t0003g0017others(218): Show | 222 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.-260-1217_-260-121 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69529622 | |||||
| chr12:69529834
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-260-1031C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69529834 | ||||||
| chr12:69529876
|
A | C | 1 | a0001c0001t0002g0335 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-260-989A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69529876 | ||||||
| chr12:69530058
|
G | GA | 7 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0298others(4): Show | 7 | HG01346.hp2 HG02615.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.-260-798dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69530058 | |||||
| chr12:69530161
|
TAACAATT others(19): Show |
T | 6 | a0001c0002t0001g0172a0001c0002t0001g0173a0001c0002t0001g0174others(3): Show | 6 | HG00639.hp2 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-260-682_-260-657d others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69530161 | |||||
| chr12:69530271
|
C | CT | 14 | a0001c0001t0001g0226a0001c0001t0002g0286a0001c0001t0002g0289others(11): Show | 14 | HG01884.hp1 HG01934.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.-260-580dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 69530271 | |||||
| chr12:69530353
|
T | A | 1 | a0001c0002t0001g0137 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-260-512T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69530353 | ||||||
| chr12:69530597
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-260-268G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69530597 | ||||||
| chr12:69530615
|
C | T | 1 | a0001c0002t0001g0156 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-260-250C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69530615 | ||||||
| chr12:69530977
|
C | CT | 12 | a0001c0001t0003g0017a0001c0001t0003g0022a0001c0001t0003g0023others(9): Show | 12 | HG00639.hp2 HG01358.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.-165+34dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 69530977 | |||||
| chr12:69530977
|
CT | C | 101 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(98): Show | 101 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-165+34delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 69530977 | |||||
| chr12:69531095
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-165+135C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | chr12 | 69531095 | ||||||
| chr12:69531273
|
T | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-165+313T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | chr12 | 69531273 | ||||||
| chr12:69531335
|
G | GA | 103 | a0001c0001t0001g0226a0001c0001t0013g0189a0001c0001t0013g0190others(100): Show | 103 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.-165+387dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 69531335 | |||||
| chr12:69531390
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-165+430A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | chr12 | 69531390 | ||||||
| chr12:69531401
|
T | G | 3 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097 | 3 | HG01123.hp2 HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-165+441T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | chr12 | 69531401 | ||||||
| chr12:69531499
|
G | A | 1 | a0001c0002t0001g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-164-515G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | chr12 | 69531499 | ||||||
| chr12:69531666
|
GA | G | 106 | a0001c0001t0001g0226a0001c0001t0013g0189a0001c0001t0013g0190others(103): Show | 106 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-164-337delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 69531666 | |||||
| chr12:69531730
|
A | G | 1 | a0001c0002t0001g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-164-284A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | chr12 | 69531730 | ||||||
| chr12:69531915
|
T | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-164-99T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 2/8 | chr12 | 69531915 | ||||||
| chr12:69532123
|
T | C | 7 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0280others(4): Show | 7 | HG02615.hp2 HG02976.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122+67T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532123 | ||||||
| chr12:69532220
|
G | A | 1 | a0001c0001t0003g0035 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-122+164G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532220 | ||||||
| chr12:69532277
|
A | G | 2 | a0001c0002t0001g0123a0001c0002t0001g0125 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-122+221A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532277 | ||||||
| chr12:69532352
|
T | C | 1 | a0001c0001t0003g0075 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-122+296T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532352 | ||||||
| chr12:69532396
|
C | T | 2 | a0001c0001t0003g0034a0001c0002t0001g0160 | 2 | HG01123.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-122+340C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532396 | ||||||
| chr12:69532738
|
T | C | 1 | a0001c0001t0023g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-122+682T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532738 | ||||||
| chr12:69532842
|
T | C | 1 | a0001c0001t0002g0203 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-122+786T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532842 | ||||||
| chr12:69532866
|
G | A | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-122+810G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532866 | ||||||
| chr12:69532924
|
G | A | 230 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(227): Show | 231 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(228): Show |
intron_variant | MODIFIER | c.-122+868G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532924 | ||||||
| chr12:69532945
|
T | G | 1 | a0001c0001t0026g0145 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-122+889T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532945 | ||||||
| chr12:69532954
|
A | G | 1 | a0001c0002t0011g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-122+898A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69532954 | ||||||
| chr12:69533354
|
G | GT | 96 | a0001c0001t0001g0226a0001c0001t0003g0230a0001c0001t0013g0189others(93): Show | 96 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-122+1310dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69533354 | |||||
| chr12:69533685
|
G | T | 2 | a0001c0002t0001g0157a0001c0002t0001g0158 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-122+1629G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69533685 | ||||||
| chr12:69533696
|
A | C | 1 | a0001c0001t0002g0301 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-122+1640A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69533696 | ||||||
| chr12:69533727
|
C | T | 1 | a0001c0002t0024g0219 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-122+1671C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69533727 | ||||||
| chr12:69533863
|
A | G | 1 | a0001c0001t0003g0024 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-122+1807A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69533863 | ||||||
| chr12:69533930
|
A | G | 2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-122+1874A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69533930 | ||||||
| chr12:69534028
|
A | G | 1 | a0001c0002t0001g0150 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-122+1972A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534028 | ||||||
| chr12:69534076
|
A | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+2020A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534076 | ||||||
| chr12:69534111
|
T | A | 2 | a0001c0002t0006g0256a0001c0002t0006g0257 | 2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-122+2055T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534111 | ||||||
| chr12:69534240
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-122+2184G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534240 | ||||||
| chr12:69534305
|
C | T | 1 | a0001c0001t0023g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-122+2249C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534305 | ||||||
| chr12:69534349
|
C | T | 11 | a0001c0001t0004g0082a0001c0001t0004g0084a0001c0001t0004g0087others(8): Show | 11 | HG01192.hp1 HG01934.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-122+2293C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534349 | ||||||
| chr12:69534420
|
G | C | 1 | a0001c0001t0003g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-122+2364G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534420 | ||||||
| chr12:69534643
|
G | A | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-122+2587G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534643 | ||||||
| chr12:69534644
|
G | A | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-122+2588G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534644 | ||||||
| chr12:69534718
|
A | G | 18 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(15): Show | 18 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-122+2662A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534718 | ||||||
| chr12:69534791
|
A | G | 1 | a0001c0002t0001g0139 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-122+2735A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69534791 | ||||||
| chr12:69535040
|
C | CTGAAATT | 7 | a0001c0001t0003g0227a0001c0001t0003g0228a0001c0001t0003g0229others(4): Show | 7 | HG00544.hp1 NA18955.hp2 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.-122+2986_-122+298 others(11): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69535040 | |||||
| chr12:69535081
|
G | C | 1 | a0001c0001t0004g0106 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-122+3025G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535081 | ||||||
| chr12:69535156
|
G | A | 1 | a0001c0002t0001g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-122+3100G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535156 | ||||||
| chr12:69535214
|
G | A | 74 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(71): Show | 74 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.-122+3158G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535214 | ||||||
| chr12:69535274
|
C | T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-122+3218C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535274 | ||||||
| chr12:69535305
|
G | A | 2 | a0001c0002t0019g0142a0001c0002t0019g0143 | 2 | HG00733.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.-122+3249G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535305 | ||||||
| chr12:69535376
|
G | A | 4 | a0001c0002t0001g0108a0001c0002t0001g0134a0001c0002t0001g0141others(1): Show | 4 | HG02056.hp2 NA18952.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-122+3320G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535376 | ||||||
| chr12:69535394
|
G | T | 20 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0273others(17): Show | 20 | HG02040.hp2 HG02071.hp1 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.-122+3338G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535394 | ||||||
| chr12:69535397
|
G | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-122+3341G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535397 | ||||||
| chr12:69535647
|
G | A | 289 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(286): Show | 290 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.-122+3591G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535647 | ||||||
| chr12:69535671
|
G | A | 7 | a0001c0001t0003g0017a0001c0001t0003g0022a0001c0001t0003g0023others(4): Show | 7 | HG01358.hp2 HG01952.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122+3615G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535671 | ||||||
| chr12:69535730
|
T | G | 1 | a0001c0002t0006g0263 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-122+3674T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535730 | ||||||
| chr12:69535862
|
T | C | 6 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0128others(3): Show | 6 | NA18954.hp2 NA18981.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.-122+3806T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69535862 | ||||||
| chr12:69535864
|
CTTTA | C | 7 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0280others(4): Show | 7 | HG02615.hp2 HG02976.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122+3816_-122+381 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69535864 | |||||
| chr12:69536101
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0004g0097 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-122+4070_-122+408 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69536101 | |||||
| chr12:69536101
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0004g0084 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-122+4066_-122+408 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69536101 | |||||
| chr12:69536102
|
T | C | 4 | a0001c0001t0003g0067a0001c0001t0003g0069a0001c0001t0003g0236others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122+4046T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536102 | ||||||
| chr12:69536112
|
TTTTTTTT others(23): Show |
T | 1 | a0001c0002t0001g0170 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-122+4057_-122+408 others(34): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536112 | ||||||
| chr12:69536113
|
T | C | 1 | a0001c0002t0001g0133 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-122+4057T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536113 | ||||||
| chr12:69536113
|
TTTTTTTT others(22): Show |
T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+4058_-122+408 others(33): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536113 | ||||||
| chr12:69536114
|
TTTTTTTT others(21): Show |
T | 1 | a0001c0001t0003g0232 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-122+4059_-122+408 others(32): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536114 | ||||||
| chr12:69536119
|
TTTTTTTT others(16): Show |
T | 1 | a0001c0002t0001g0174 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-122+4064_-122+408 others(27): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536119 | ||||||
| chr12:69536121
|
TTTTTTTT others(14): Show |
T | 11 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0280others(8): Show | 11 | HG01069.hp1 HG02074.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-122+4066_-122+408 others(25): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536121 | ||||||
| chr12:69536122
|
TTTTTTTT others(13): Show |
T | 2 | a0001c0001t0005g0012a0001c0001t0025g0013 | 2 | HG01361.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-122+4067_-122+408 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536122 | ||||||
| chr12:69536123
|
TTTTTTTT others(12): Show |
T | 1 | a0001c0002t0007g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-122+4068_-122+408 others(23): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536123 | ||||||
| chr12:69536126
|
TTTTTTTT others(9): Show |
T | 7 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(4): Show | 7 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-122+4071_-122+408 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536126 | ||||||
| chr12:69536127
|
TTTTTTTT others(8): Show |
T | 1 | a0001c0001t0008g0006 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-122+4072_-122+408 others(19): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536127 | ||||||
| chr12:69536129
|
TTTTTTTT others(6): Show |
T | 20 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(17): Show | 20 | HG01109.hp2 HG01167.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-122+4074_-122+408 others(17): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536129 | ||||||
| chr12:69536130
|
TTTTTTTT others(5): Show |
T | 6 | a0001c0001t0005g0244a0001c0002t0001g0108a0001c0002t0001g0125others(3): Show | 6 | HG01070.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-122+4075_-122+408 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536130 | ||||||
| chr12:69536131
|
TTTTTTTT others(4): Show |
T | 68 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191others(65): Show | 68 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-122+4076_-122+408 others(15): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536131 | ||||||
| chr12:69536132
|
TTTTTTTT others(3): Show |
T | 25 | a0001c0001t0002g0275a0001c0001t0003g0067a0001c0001t0015g0153others(22): Show | 25 | HG00558.hp1 HG00735.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.-122+4077_-122+408 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536132 | ||||||
| chr12:69536136
|
TTTTTTG | T | 37 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0277others(34): Show | 37 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-122+4081_-122+408 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536136 | ||||||
| chr12:69536137
|
TTTTTG | T | 39 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(36): Show | 39 | HG00733.hp1 HG01256.hp2 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.-122+4082_-122+408 others(9): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536137 | ||||||
| chr12:69536138
|
TTTTG | T | 39 | a0001c0001t0002g0205a0001c0001t0002g0269a0001c0001t0002g0270others(36): Show | 39 | HG00597.hp2 HG00673.hp1 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.-122+4083_-122+408 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536138 | ||||||
| chr12:69536139
|
TTTG | T | 11 | a0001c0001t0002g0294a0001c0001t0002g0300a0001c0001t0002g0320others(8): Show | 11 | HG00408.hp2 HG01258.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-122+4084_-122+408 others(7): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536139 | ||||||
| chr12:69536142
|
G | T | 5 | a0001c0001t0003g0057a0001c0001t0003g0068a0001c0001t0003g0069others(2): Show | 5 | HG02486.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-122+4086G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536142 | ||||||
| chr12:69536164
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+4108A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536164 | ||||||
| chr12:69536180
|
A | G | 2 | a0001c0002t0001g0131a0001c0002t0001g0192 | 2 | NA18961.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-122+4124A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536180 | ||||||
| chr12:69536280
|
A | G | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-122+4224A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536280 | ||||||
| chr12:69536340
|
T | A | 18 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191others(15): Show | 18 | HG00408.hp1 HG00733.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-122+4284T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536340 | ||||||
| chr12:69536418
|
C | T | 2 | a0001c0002t0007g0119a0001c0002t0007g0211 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-122+4362C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536418 | ||||||
| chr12:69536554
|
G | A | 1 | a0001c0002t0011g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-122+4498G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536554 | ||||||
| chr12:69536576
|
TTA | T | 23 | a0001c0001t0002g0286a0001c0001t0002g0289a0001c0001t0002g0297others(20): Show | 23 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.-122+4521_-122+452 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536576 | ||||||
| chr12:69536578
|
A | T | 12 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(9): Show | 12 | HG00735.hp2 HG01167.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-122+4522A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536578 | ||||||
| chr12:69536579
|
AT | A | 202 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(199): Show | 203 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(200): Show |
intron_variant | MODIFIER | c.-122+4534delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69536579 | |||||
| chr12:69536580
|
T | A | 35 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(32): Show | 35 | HG00735.hp2 HG01069.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.-122+4524T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536580 | ||||||
| chr12:69536590
|
T | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+4534T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536590 | ||||||
| chr12:69536592
|
T | C | 1 | a0001c0001t0002g0276 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-122+4536T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536592 | ||||||
| chr12:69536616
|
G | C | 1 | a0001c0001t0008g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-122+4560G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536616 | ||||||
| chr12:69536649
|
T | C | 238 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(235): Show | 239 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(236): Show |
intron_variant | MODIFIER | c.-122+4593T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536649 | ||||||
| chr12:69536656
|
C | T | 80 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(77): Show | 80 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-122+4600C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536656 | ||||||
| chr12:69536703
|
T | C | 4 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0044others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122+4647T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536703 | ||||||
| chr12:69536964
|
T | C | 7 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0280others(4): Show | 7 | HG02615.hp2 HG02976.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122+4908T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536964 | ||||||
| chr12:69536965
|
A | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-122+4909A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69536965 | ||||||
| chr12:69537187
|
T | C | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-122+5131T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69537187 | ||||||
| chr12:69537337
|
AT | A | 217 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(214): Show | 217 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(214): Show |
intron_variant | MODIFIER | c.-122+5292delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69537337 | |||||
| chr12:69537473
|
G | A | 2 | a0001c0001t0005g0012a0001c0001t0029g0206 | 2 | HG01069.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-122+5417G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69537473 | ||||||
| chr12:69537490
|
G | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+5434G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69537490 | ||||||
| chr12:69537606
|
T | C | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-122+5550T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69537606 | ||||||
| chr12:69537610
|
T | C | 1 | a0001c0001t0002g0278 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-122+5554T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69537610 | ||||||
| chr12:69537979
|
G | A | 231 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(228): Show | 232 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(229): Show |
intron_variant | MODIFIER | c.-122+5923G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69537979 | ||||||
| chr12:69538074
|
G | A | 5 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191others(2): Show | 5 | HG00408.hp1 HG01928.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.-122+6018G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538074 | ||||||
| chr12:69538101
|
A | G | 1 | a0001c0002t0001g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-122+6045A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538101 | ||||||
| chr12:69538195
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0009g0337 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-122+6140_-122+614 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538195 | |||||
| chr12:69538195
|
T | TTATATAT others(15): Show |
1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-122+6140_-122+614 others(26): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538195 | |||||
| chr12:69538195
|
TTTTATAT others(5): Show |
T | 78 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(75): Show | 78 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-122+6141_-122+615 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538195 | |||||
| chr12:69538197
|
T | A | 13 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-122+6141T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538197 | ||||||
| chr12:69538197
|
T | TTATA | 9 | a0001c0001t0004g0103a0001c0002t0001g0110a0001c0002t0001g0114others(6): Show | 9 | HG00544.hp2 HG01192.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-122+6164_-122+616 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATA | 8 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(5): Show | 8 | HG00099.hp2 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+6162_-122+616 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(1): Show |
5 | a0001c0001t0009g0338a0001c0001t0009g0339a0001c0001t0009g0340others(2): Show | 5 | HG02145.hp2 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-122+6160_-122+616 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(3): Show |
4 | a0001c0001t0005g0245a0001c0001t0009g0336a0001c0001t0033g0242others(1): Show | 4 | HG02647.hp2 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122+6158_-122+616 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(5): Show |
6 | a0001c0001t0005g0012a0001c0001t0005g0247a0001c0001t0005g0248others(3): Show | 6 | HG01109.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-122+6156_-122+616 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(7): Show |
2 | a0001c0002t0001g0108a0001c0002t0001g0120 | 2 | HG03579.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-122+6154_-122+616 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(9): Show |
7 | a0001c0001t0001g0226a0001c0001t0005g0246a0001c0001t0015g0153others(4): Show | 7 | HG01069.hp1 HG01123.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-122+6152_-122+616 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(11): Show |
10 | a0001c0002t0001g0117a0001c0002t0001g0125a0001c0002t0001g0137others(7): Show | 10 | HG00639.hp2 HG01258.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-122+6150_-122+616 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(13): Show |
16 | a0001c0001t0026g0145a0001c0001t0031g0014a0001c0002t0001g0128others(13): Show | 16 | HG00408.hp1 HG00733.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-122+6148_-122+616 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(15): Show |
20 | a0001c0002t0001g0127a0001c0002t0001g0129a0001c0002t0001g0151others(17): Show | 20 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.-122+6146_-122+616 others(26): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(17): Show |
16 | a0001c0001t0013g0191a0001c0002t0001g0122a0001c0002t0001g0130others(13): Show | 16 | HG01433.hp2 HG01928.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-122+6144_-122+616 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(19): Show |
10 | a0001c0001t0013g0190a0001c0002t0001g0118a0001c0002t0001g0126others(7): Show | 10 | HG00558.hp2 HG00735.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-122+6142_-122+616 others(30): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(21): Show |
11 | a0001c0001t0005g0015a0001c0001t0013g0189a0001c0001t0025g0013others(8): Show | 11 | HG01361.hp1 HG01361.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-122+6167_-122+616 others(32): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(23): Show |
6 | a0001c0002t0001g0135a0001c0002t0001g0171a0001c0002t0001g0179others(3): Show | 6 | HG00609.hp1 HG02055.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-122+6167_-122+616 others(34): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
T | TTATATAT others(29): Show |
1 | a0001c0002t0001g0124 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-122+6167_-122+616 others(40): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538197
|
TTATATAT others(3): Show |
T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+6158_-122+616 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538197 | |||||
| chr12:69538199
|
A | ATATATAT others(17): Show |
1 | a0001c0002t0001g0202 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-122+6166_-122+616 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538199 | |||||
| chr12:69538212
|
TATATATA others(30): Show |
T | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-122+6168_-122+620 others(41): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538212 | |||||
| chr12:69538214
|
TATATATA others(28): Show |
T | 40 | a0001c0001t0002g0203a0001c0001t0002g0271a0001c0001t0002g0272others(37): Show | 40 | HG00597.hp2 HG01934.hp2 HG01952.hp1 others(37): Show |
intron_variant | MODIFIER | c.-122+6168_-122+620 others(39): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538214 | |||||
| chr12:69538216
|
TATATATA others(26): Show |
T | 21 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0269others(18): Show | 21 | HG00609.hp2 HG00673.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.-122+6168_-122+620 others(37): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538216 | |||||
| chr12:69538218
|
TATATAGC others(24): Show |
T | 8 | a0001c0001t0002g0270a0001c0001t0002g0280a0001c0001t0002g0281others(5): Show | 8 | HG02976.hp1 HG03041.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+6168_-122+619 others(35): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538218 | |||||
| chr12:69538220
|
TATAGCAT others(22): Show |
T | 2 | a0001c0001t0002g0275a0001c0001t0002g0310 | 2 | HG00558.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.-122+6168_-122+619 others(33): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538220 | |||||
| chr12:69538223
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0020g0224 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-122+6167_-122+616 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538223 | ||||||
| chr12:69538223
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0008g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-122+6167_-122+616 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538223 | ||||||
| chr12:69538223
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0008g0003a0001c0001t0008g0007 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-122+6167_-122+616 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538223 | ||||||
| chr12:69538223
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0008g0004a0001c0001t0008g0006 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-122+6167_-122+616 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538223 | ||||||
| chr12:69538223
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0020g0225 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-122+6167_-122+616 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538223 | ||||||
| chr12:69538234
|
T | TTA | 3 | a0001c0001t0004g0209a0001c0002t0001g0157a0001c0002t0001g0158 | 3 | HG01167.hp1 HG01169.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-122+6191_-122+619 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538234 | |||||
| chr12:69538234
|
TTA | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+6191_-122+619 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538234 | |||||
| chr12:69538247
|
T | C | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+6191T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538247 | ||||||
| chr12:69538361
|
C | T | 5 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02976.hp1 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-122+6305C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538361 | ||||||
| chr12:69538380
|
A | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-122+6324A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538380 | ||||||
| chr12:69538447
|
A | AATTCATG others(31): Show |
3 | a0001c0002t0001g0126a0001c0002t0001g0127a0001c0002t0001g0130 | 3 | NA18981.hp2 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-122+6468_-122+650 others(42): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538447 | |||||
| chr12:69538527
|
C | T | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-122+6471C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538527 | ||||||
| chr12:69538574
|
A | AGTGTGTG others(10): Show |
8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+6519_-122+653 others(21): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69538574 | |||||
| chr12:69538624
|
A | G | 1 | a0001c0002t0006g0257 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-122+6568A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538624 | ||||||
| chr12:69538648
|
A | G | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+6592A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538648 | ||||||
| chr12:69538764
|
A | G | 109 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-122+6708A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538764 | ||||||
| chr12:69538768
|
T | C | 109 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-122+6712T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538768 | ||||||
| chr12:69538854
|
G | A | 1 | a0001c0001t0023g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-122+6798G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538854 | ||||||
| chr12:69538897
|
A | G | 5 | a0001c0002t0007g0121a0001c0002t0007g0154a0001c0002t0007g0155others(2): Show | 5 | HG00741.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-122+6841A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538897 | ||||||
| chr12:69538925
|
G | A | 2 | a0001c0001t0002g0305a0001c0001t0002g0310 | 2 | NA18964.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-122+6869G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538925 | ||||||
| chr12:69538955
|
C | T | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-122+6899C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538955 | ||||||
| chr12:69538960
|
C | T | 74 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(71): Show | 74 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.-122+6904C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538960 | ||||||
| chr12:69538984
|
C | A | 1 | a0001c0001t0003g0233 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-122+6928C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69538984 | ||||||
| chr12:69539136
|
A | G | 14 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-122+7080A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539136 | ||||||
| chr12:69539246
|
T | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-122+7190T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539246 | ||||||
| chr12:69539393
|
G | T | 1 | a0001c0002t0001g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-122+7337G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539393 | ||||||
| chr12:69539419
|
A | G | 91 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(88): Show | 91 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-122+7363A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539419 | ||||||
| chr12:69539460
|
A | G | 1 | a0001c0001t0010g0094 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-122+7404A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539460 | ||||||
| chr12:69539484
|
C | A | 1 | a0001c0002t0024g0219 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-122+7428C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539484 | ||||||
| chr12:69539500
|
G | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-122+7444G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539500 | ||||||
| chr12:69539727
|
G | A | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-122+7671G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539727 | ||||||
| chr12:69539799
|
C | G | 80 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(77): Show | 80 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-122+7743C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539799 | ||||||
| chr12:69539904
|
G | A | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+7848G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539904 | ||||||
| chr12:69539992
|
G | A | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+7936G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69539992 | ||||||
| chr12:69540125
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-122+8069C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540125 | ||||||
| chr12:69540133
|
G | A | 13 | a0001c0002t0001g0108a0001c0002t0001g0124a0001c0002t0001g0134others(10): Show | 13 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.-122+8077G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540133 | ||||||
| chr12:69540239
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-122+8183C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540239 | ||||||
| chr12:69540272
|
A | T | 1 | a0001c0001t0027g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-122+8216A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540272 | ||||||
| chr12:69540282
|
A | T | 1 | a0001c0002t0001g0202 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-122+8226A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540282 | ||||||
| chr12:69540335
|
C | CAA | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+8289_-122+829 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69540335 | |||||
| chr12:69540336
|
A | C | 107 | a0001c0001t0001g0226a0001c0001t0013g0189a0001c0001t0013g0190others(104): Show | 107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-122+8280A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540336 | ||||||
| chr12:69540387
|
A | G | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-122+8331A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540387 | ||||||
| chr12:69540395
|
G | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+8339G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540395 | ||||||
| chr12:69540435
|
G | A | 5 | a0001c0002t0001g0120a0001c0002t0011g0109a0001c0002t0011g0111others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-122+8379G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540435 | ||||||
| chr12:69540493
|
CA | C | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-122+8438delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540493 | ||||||
| chr12:69540808
|
G | A | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-122+8752G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69540808 | ||||||
| chr12:69541136
|
AC | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-122+9081delC | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69541136 | ||||||
| chr12:69541182
|
C | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | HG03041.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-122+9126C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69541182 | ||||||
| chr12:69541214
|
G | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+9158G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69541214 | ||||||
| chr12:69541370
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-122+9314G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69541370 | ||||||
| chr12:69541402
|
G | A | 231 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(228): Show | 232 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(229): Show |
intron_variant | MODIFIER | c.-122+9346G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69541402 | ||||||
| chr12:69541428
|
A | C | 1 | a0001c0001t0004g0087 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-122+9372A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69541428 | ||||||
| chr12:69541611
|
A | G | 92 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(89): Show | 92 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.-122+9555A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69541611 | ||||||
| chr12:69541684
|
A | T | 1 | a0001c0001t0005g0240 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-122+9628A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69541684 | ||||||
| chr12:69541824
|
CA | C | 9 | a0001c0001t0002g0205a0001c0001t0002g0333a0001c0001t0003g0021others(6): Show | 9 | HG01891.hp1 HG02027.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.-122+9790delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69541824 | |||||
| chr12:69541824
|
CAA | C | 214 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(211): Show | 215 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(212): Show |
intron_variant | MODIFIER | c.-122+9789_-122+979 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69541824 | |||||
| chr12:69541824
|
CAAA | C | 11 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(8): Show | 11 | HG01167.hp2 HG02976.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.-122+9788_-122+979 others(7): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69541824 | |||||
| chr12:69541944
|
A | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-122+9888A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69541944 | ||||||
| chr12:69541983
|
A | G | 1 | a0001c0001t0003g0057 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-122+9927A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69541983 | ||||||
| chr12:69542120
|
C | T | 18 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191others(15): Show | 18 | HG00408.hp1 HG00733.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-122+10064C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69542120 | ||||||
| chr12:69542158
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-122+10102A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69542158 | ||||||
| chr12:69542321
|
G | A | 78 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(75): Show | 78 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-122+10265G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69542321 | ||||||
| chr12:69542381
|
G | A | 3 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191 | 3 | NA18946.hp1 NA18988.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-122+10325G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69542381 | ||||||
| chr12:69542522
|
C | CA | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-122+10469dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69542522 | |||||
| chr12:69542768
|
A | G | 1 | a0001c0001t0005g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-122+10712A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69542768 | ||||||
| chr12:69542809
|
G | A | 66 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(63): Show | 66 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-122+10753G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69542809 | ||||||
| chr12:69542954
|
T | C | 339 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(336): Show | 340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.-122+10898T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69542954 | ||||||
| chr12:69542987
|
A | G | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-122+10931A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69542987 | ||||||
| chr12:69543075
|
C | G | 1 | a0001c0002t0018g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-122+11019C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543075 | ||||||
| chr12:69543085
|
A | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-122+11029A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543085 | ||||||
| chr12:69543139
|
C | T | 231 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(228): Show | 232 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(229): Show |
intron_variant | MODIFIER | c.-122+11083C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543139 | ||||||
| chr12:69543184
|
T | C | 1 | a0001c0002t0007g0154 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-122+11128T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543184 | ||||||
| chr12:69543220
|
A | G | 1 | a0001c0001t0003g0076 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-122+11164A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543220 | ||||||
| chr12:69543466
|
G | A | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+11410G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543466 | ||||||
| chr12:69543467
|
A | G | 8 | a0001c0002t0007g0113a0001c0002t0007g0119a0001c0002t0007g0121others(5): Show | 8 | HG00741.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+11411A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543467 | ||||||
| chr12:69543625
|
A | G | 2 | a0001c0002t0001g0160a0001c0002t0001g0181 | 2 | HG01123.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-122+11569A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543625 | ||||||
| chr12:69543724
|
A | G | 22 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(19): Show | 22 | HG00544.hp1 HG00673.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.-122+11668A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543724 | ||||||
| chr12:69543856
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-122+11800A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543856 | ||||||
| chr12:69543964
|
C | T | 2 | a0001c0002t0007g0155a0001c0002t0007g0166 | 2 | HG02258.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-122+11908C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543964 | ||||||
| chr12:69543988
|
A | G | 1 | a0001c0001t0002g0316 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-122+11932A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543988 | ||||||
| chr12:69543994
|
A | G | 18 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(15): Show | 18 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-122+11938A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69543994 | ||||||
| chr12:69544018
|
T | C | 1 | a0001c0002t0001g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-122+11962T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544018 | ||||||
| chr12:69544084
|
C | CG | 11 | a0001c0001t0002g0270a0001c0001t0002g0334a0001c0001t0002g0335others(8): Show | 11 | HG00673.hp2 HG00741.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-122+12035dupG | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69544084 | |||||
| chr12:69544087
|
G | T | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-122+12031G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544087 | ||||||
| chr12:69544099
|
G | C | 2 | a0001c0001t0014g0009a0001c0001t0014g0010 | 2 | HG01167.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-122+12043G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544099 | ||||||
| chr12:69544104
|
CT | C | 7 | a0001c0001t0002g0321a0001c0001t0005g0015a0001c0001t0005g0247others(4): Show | 7 | HG01069.hp1 HG01069.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-122+12062delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69544104 | |||||
| chr12:69544131
|
A | G | 1 | a0001c0001t0002g0288 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-122+12075A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544131 | ||||||
| chr12:69544173
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+12117A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544173 | ||||||
| chr12:69544292
|
A | G | 1 | a0001c0002t0001g0122 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-122+12236A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544292 | ||||||
| chr12:69544300
|
A | G | 1 | a0001c0001t0002g0307 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-122+12244A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544300 | ||||||
| chr12:69544703
|
T | C | 1 | a0001c0001t0027g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-122+12647T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544703 | ||||||
| chr12:69544738
|
A | G | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-122+12682A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544738 | ||||||
| chr12:69544739
|
G | T | 1 | a0001c0001t0002g0275 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-122+12683G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544739 | ||||||
| chr12:69544754
|
G | A | 200 | a0001c0001t0002g0309a0001c0001t0003g0016a0001c0001t0003g0017others(197): Show | 201 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-122+12698G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544754 | ||||||
| chr12:69545155
|
T | A | 285 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(282): Show | 286 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.-122+13099T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545155 | ||||||
| chr12:69545277
|
C | T | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-122+13221C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545277 | ||||||
| chr12:69545330
|
A | G | 17 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(14): Show | 17 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-122+13274A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545330 | ||||||
| chr12:69545344
|
G | C | 1 | a0001c0001t0002g0317 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-122+13288G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545344 | ||||||
| chr12:69545394
|
C | T | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-122+13338C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545394 | ||||||
| chr12:69545422
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+13366C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545422 | ||||||
| chr12:69545465
|
A | G | 1 | a0001c0001t0002g0283 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-122+13409A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545465 | ||||||
| chr12:69545575
|
T | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+13519T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545575 | ||||||
| chr12:69545618
|
G | T | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-122+13562G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545618 | ||||||
| chr12:69545711
|
G | A | 1 | a0001c0001t0008g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-122+13655G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545711 | ||||||
| chr12:69545735
|
G | A | 1 | a0001c0002t0011g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-122+13679G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545735 | ||||||
| chr12:69545755
|
C | CA | 38 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0003g0021others(35): Show | 38 | HG00735.hp2 HG01123.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.-122+13722dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69545755 | |||||
| chr12:69545755
|
CA | C | 138 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(135): Show | 138 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.-122+13722delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69545755 | |||||
| chr12:69545755
|
CAA | C | 8 | a0001c0001t0003g0067a0001c0001t0003g0068a0001c0001t0003g0069others(5): Show | 8 | HG02451.hp2 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+13721_-122+13 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69545755 | |||||
| chr12:69545755
|
CAAAA | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+13719_-122+13 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69545755 | |||||
| chr12:69545765
|
A | C | 1 | a0001c0001t0005g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-122+13709A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545765 | ||||||
| chr12:69545768
|
A | C | 4 | a0001c0002t0001g0135a0001c0002t0001g0137a0001c0002t0001g0150others(1): Show | 4 | HG00609.hp1 NA18945.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-122+13712A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545768 | ||||||
| chr12:69545772
|
A | C | 114 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(111): Show | 115 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.-122+13716A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545772 | ||||||
| chr12:69545773
|
A | C | 8 | a0001c0002t0007g0113a0001c0002t0007g0119a0001c0002t0007g0121others(5): Show | 8 | HG00741.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-122+13717A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545773 | ||||||
| chr12:69545778
|
AC | A | 20 | a0001c0001t0003g0016a0001c0001t0003g0035a0001c0001t0003g0036others(17): Show | 20 | HG00140.hp1 HG00408.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.-122+13723delC | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545778 | ||||||
| chr12:69545779
|
C | A | 22 | a0001c0001t0001g0226a0001c0001t0003g0033a0001c0001t0003g0034others(19): Show | 22 | HG00733.hp1 HG00735.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.-122+13723C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545779 | ||||||
| chr12:69545785
|
C | A | 1 | a0001c0001t0015g0055 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-122+13729C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545785 | ||||||
| chr12:69545954
|
ATTAAC | A | 4 | a0001c0002t0001g0146a0001c0002t0001g0167a0001c0002t0001g0168others(1): Show | 4 | HG00099.hp2 HG02970.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122+13903_-122+13 others(11): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69545954 | |||||
| chr12:69545985
|
T | C | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-122+13929T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69545985 | ||||||
| chr12:69546101
|
A | G | 1 | a0001c0002t0001g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-122+14045A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69546101 | ||||||
| chr12:69546260
|
G | T | 1 | a0001c0001t0002g0326 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-122+14204G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69546260 | ||||||
| chr12:69546311
|
G | A | 4 | a0001c0002t0011g0109a0001c0002t0011g0111a0001c0002t0011g0112others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-122+14255G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69546311 | ||||||
| chr12:69546458
|
A | G | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+14402A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69546458 | ||||||
| chr12:69546469
|
G | C | 1 | a0001c0001t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-122+14413G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69546469 | ||||||
| chr12:69546535
|
A | C | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-122+14479A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69546535 | ||||||
| chr12:69546777
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-122+14721G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69546777 | ||||||
| chr12:69546925
|
T | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-122+14869T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69546925 | ||||||
| chr12:69547047
|
A | G | 113 | a0001c0001t0001g0226a0001c0001t0009g0336a0001c0001t0009g0337others(110): Show | 113 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.-122+14991A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69547047 | ||||||
| chr12:69547235
|
G | A | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-121-14945G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69547235 | ||||||
| chr12:69547291
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-121-14889C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69547291 | ||||||
| chr12:69547481
|
C | T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-121-14699C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69547481 | ||||||
| chr12:69547485
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-121-14695A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69547485 | ||||||
| chr12:69547718
|
T | C | 7 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0280others(4): Show | 7 | HG02615.hp2 HG02976.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121-14462T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69547718 | ||||||
| chr12:69547719
|
G | C | 305 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(302): Show | 306 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.-121-14461G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69547719 | ||||||
| chr12:69547786
|
A | G | 229 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(226): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.-121-14394A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69547786 | ||||||
| chr12:69547830
|
C | CT | 79 | a0001c0001t0002g0314a0001c0001t0002g0316a0001c0001t0003g0016others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-121-14324dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69547830 | |||||
| chr12:69547830
|
C | CTT | 78 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(75): Show | 78 | HG00558.hp1 HG00609.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.-121-14325_-121-14 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69547830 | |||||
| chr12:69547830
|
C | CTTT | 17 | a0001c0001t0002g0204a0001c0001t0002g0208a0001c0001t0002g0269others(14): Show | 17 | HG00597.hp2 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.-121-14326_-121-14 others(9): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69547830 | |||||
| chr12:69547830
|
C | CTTTT | 9 | a0001c0001t0002g0205a0001c0001t0002g0266a0001c0001t0002g0267others(6): Show | 9 | HG01167.hp2 HG02615.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.-121-14327_-121-14 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69547830 | |||||
| chr12:69547830
|
CT | C | 18 | a0001c0001t0005g0015a0001c0001t0005g0239a0001c0001t0005g0241others(15): Show | 18 | HG01109.hp2 HG02055.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-121-14324delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69547830 | |||||
| chr12:69547830
|
CTT | C | 7 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(4): Show | 7 | HG01069.hp1 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121-14325_-121-14 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69547830 | |||||
| chr12:69547830
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0003g0026a0001c0001t0003g0030a0001c0001t0003g0031others(1): Show | 4 | HG00673.hp2 NA18960.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121-14333_-121-14 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69547830 | |||||
| chr12:69547830
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0001g0156a0001c0002t0024g0219 | 2 | NA18747.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-121-14334_-121-14 others(17): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69547830 | |||||
| chr12:69547830
|
CTTTTTTT others(5): Show |
C | 108 | a0001c0001t0001g0226a0001c0001t0009g0336a0001c0001t0009g0337others(105): Show | 108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-121-14335_-121-14 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69547830 | |||||
| chr12:69548067
|
G | A | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-121-14113G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69548067 | ||||||
| chr12:69548113
|
G | A | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-121-14067G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69548113 | ||||||
| chr12:69548237
|
T | C | 73 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(70): Show | 73 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-121-13943T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69548237 | ||||||
| chr12:69548379
|
G | A | 19 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(16): Show | 19 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.-121-13801G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69548379 | ||||||
| chr12:69548613
|
G | A | 256 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(253): Show | 257 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(254): Show |
intron_variant | MODIFIER | c.-121-13567G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69548613 | ||||||
| chr12:69548658
|
A | G | 1 | a0001c0002t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-121-13522A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69548658 | ||||||
| chr12:69548784
|
C | T | 231 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(228): Show | 232 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(229): Show |
intron_variant | MODIFIER | c.-121-13396C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69548784 | ||||||
| chr12:69548803
|
G | C | 14 | a0001c0001t0003g0069a0001c0001t0005g0239a0001c0001t0005g0240others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-121-13377G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69548803 | ||||||
| chr12:69549323
|
T | G | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-121-12857T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69549323 | ||||||
| chr12:69549436
|
GA | G | 231 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(228): Show | 232 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(229): Show |
intron_variant | MODIFIER | c.-121-12736delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69549436 | |||||
| chr12:69549440
|
A | G | 1 | a0001c0001t0009g0337 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-121-12740A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69549440 | ||||||
| chr12:69549459
|
G | A | 1 | a0001c0001t0003g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-121-12721G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69549459 | ||||||
| chr12:69549995
|
C | T | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-121-12185C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69549995 | ||||||
| chr12:69550453
|
T | C | 1 | a0001c0002t0001g0265 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-121-11727T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69550453 | ||||||
| chr12:69550508
|
G | A | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-121-11672G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69550508 | ||||||
| chr12:69550575
|
C | T | 9 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(6): Show | 10 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.-121-11605C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69550575 | ||||||
| chr12:69551141
|
C | T | 217 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(214): Show | 217 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(214): Show |
intron_variant | MODIFIER | c.-121-11039C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69551141 | ||||||
| chr12:69551383
|
AGT | A | 226 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(223): Show | 227 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.-121-10796_-121-10 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69551383 | ||||||
| chr12:69551482
|
T | C | 1 | a0001c0002t0001g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-121-10698T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69551482 | ||||||
| chr12:69551583
|
C | T | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-121-10597C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69551583 | ||||||
| chr12:69551742
|
G | A | 4 | a0001c0001t0003g0036a0001c0001t0003g0049a0001c0001t0003g0072others(1): Show | 4 | HG02056.hp1 HG02165.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121-10438G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69551742 | ||||||
| chr12:69551770
|
T | C | 14 | a0001c0002t0001g0262a0001c0002t0006g0001a0001c0002t0006g0252others(11): Show | 15 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-121-10410T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69551770 | ||||||
| chr12:69552002
|
A | G | 2 | a0001c0002t0001g0123a0001c0002t0001g0125 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-121-10178A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552002 | ||||||
| chr12:69552015
|
G | A | 226 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(223): Show | 227 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.-121-10165G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552015 | ||||||
| chr12:69552103
|
C | T | 1 | a0001c0002t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-121-10077C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552103 | ||||||
| chr12:69552302
|
C | CA | 54 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(51): Show | 54 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-121-9853dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69552302 | |||||
| chr12:69552302
|
C | CAA | 89 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0003g0020others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-121-9854_-121-985 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69552302 | |||||
| chr12:69552302
|
C | CAAA | 34 | a0001c0001t0001g0226a0001c0001t0002g0282a0001c0001t0003g0017others(31): Show | 34 | HG00544.hp1 HG00673.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-121-9855_-121-985 others(7): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69552302 | |||||
| chr12:69552302
|
C | CAAAA | 7 | a0001c0001t0003g0228a0001c0001t0003g0229a0001c0001t0008g0002others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121-9856_-121-985 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69552302 | |||||
| chr12:69552302
|
CA | C | 69 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0269others(66): Show | 69 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-121-9853delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69552302 | |||||
| chr12:69552302
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0023g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-121-9863_-121-985 others(15): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69552302 | |||||
| chr12:69552303
|
A | C | 2 | a0001c0002t0001g0123a0001c0002t0001g0125 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-121-9877A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552303 | ||||||
| chr12:69552343
|
G | T | 88 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191others(85): Show | 88 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-121-9837G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552343 | ||||||
| chr12:69552385
|
A | T | 4 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0175others(1): Show | 4 | HG00639.hp2 HG02615.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121-9795A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552385 | ||||||
| chr12:69552413
|
T | C | 2 | a0001c0001t0003g0051a0001c0001t0036g0046 | 2 | HG00140.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-121-9767T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552413 | ||||||
| chr12:69552422
|
C | T | 1 | a0001c0002t0001g0137 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-121-9758C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552422 | ||||||
| chr12:69552598
|
G | A | 8 | a0001c0002t0007g0113a0001c0002t0007g0119a0001c0002t0007g0121others(5): Show | 8 | HG00741.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-121-9582G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552598 | ||||||
| chr12:69552651
|
A | G | 1 | a0001c0002t0001g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-121-9529A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552651 | ||||||
| chr12:69552674
|
C | T | 1 | a0001c0001t0004g0090 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-121-9506C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552674 | ||||||
| chr12:69552679
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-121-9501G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552679 | ||||||
| chr12:69552752
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-121-9428C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552752 | ||||||
| chr12:69552781
|
A | G | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-121-9399A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552781 | ||||||
| chr12:69552882
|
A | C | 17 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(14): Show | 17 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-121-9298A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552882 | ||||||
| chr12:69552887
|
A | G | 1 | a0001c0001t0030g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-121-9293A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552887 | ||||||
| chr12:69552891
|
C | CA | 15 | a0001c0001t0002g0333a0001c0002t0001g0262a0001c0002t0006g0001others(12): Show | 16 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-121-9276dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69552891 | |||||
| chr12:69552907
|
A | G | 2 | a0001c0001t0017g0302a0001c0001t0017g0303 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-121-9273A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69552907 | ||||||
| chr12:69553017
|
A | T | 1 | a0001c0001t0008g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-121-9163A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69553017 | ||||||
| chr12:69553055
|
A | ATTTTTGT others(5): Show |
15 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(12): Show | 15 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-121-9107_-121-909 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69553055 | |||||
| chr12:69553055
|
A | ATTTTTGT others(11): Show |
1 | a0001c0001t0025g0013 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-121-9113_-121-909 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69553055 | |||||
| chr12:69553061
|
G | GTTTTTGT others(6): Show |
1 | a0001c0001t0029g0206 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-121-9114_-121-910 others(17): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69553061 | |||||
| chr12:69553077
|
T | C | 1 | a0001c0001t0009g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-121-9103T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69553077 | ||||||
| chr12:69553140
|
C | T | 1 | a0001c0001t0031g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-121-9040C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69553140 | ||||||
| chr12:69553210
|
T | C | 4 | a0001c0001t0003g0036a0001c0001t0003g0049a0001c0001t0003g0072others(1): Show | 4 | HG02056.hp1 HG02165.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121-8970T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69553210 | ||||||
| chr12:69553522
|
ATTG | A | 3 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191 | 3 | NA18946.hp1 NA18988.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-121-8654_-121-865 others(7): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69553522 | |||||
| chr12:69553571
|
G | A | 219 | a0001c0001t0001g0226a0001c0001t0003g0016a0001c0001t0003g0017others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-121-8609G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69553571 | ||||||
| chr12:69553621
|
A | T | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-121-8559A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69553621 | ||||||
| chr12:69554245
|
A | G | 10 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(7): Show | 10 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-121-7935A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69554245 | ||||||
| chr12:69554310
|
T | C | 2 | a0001c0002t0001g0137a0001c0002t0001g0150 | 2 | NA18945.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-121-7870T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69554310 | ||||||
| chr12:69554312
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-121-7868A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69554312 | ||||||
| chr12:69554406
|
G | T | 212 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(209): Show | 213 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(210): Show |
intron_variant | MODIFIER | c.-121-7774G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69554406 | ||||||
| chr12:69554853
|
C | T | 1 | a0001c0002t0006g0264 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-121-7327C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69554853 | ||||||
| chr12:69555030
|
A | AT | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-121-7141dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69555030 | |||||
| chr12:69555335
|
G | T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-121-6845G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555335 | ||||||
| chr12:69555338
|
C | A | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-121-6842C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555338 | ||||||
| chr12:69555346
|
T | C | 3 | a0001c0001t0008g0005a0001c0001t0008g0006a0001c0001t0008g0007 | 3 | HG02622.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-121-6834T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555346 | ||||||
| chr12:69555413
|
A | G | 1 | a0001c0001t0002g0325 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-121-6767A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555413 | ||||||
| chr12:69555510
|
G | A | 2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-121-6670G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555510 | ||||||
| chr12:69555526
|
G | A | 3 | a0001c0002t0001g0132a0001c0002t0001g0139a0001c0002t0001g0183 | 3 | NA18947.hp2 NA19054.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-121-6654G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555526 | ||||||
| chr12:69555620
|
G | A | 78 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(75): Show | 78 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-121-6560G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555620 | ||||||
| chr12:69555628
|
C | A | 2 | a0001c0001t0005g0012a0001c0001t0029g0206 | 2 | HG01069.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-121-6552C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555628 | ||||||
| chr12:69555683
|
A | T | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-121-6497A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555683 | ||||||
| chr12:69555755
|
A | C | 1 | a0001c0001t0002g0294 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-121-6425A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555755 | ||||||
| chr12:69555761
|
A | G | 1 | a0001c0002t0018g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-121-6419A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555761 | ||||||
| chr12:69555770
|
T | G | 1 | a0001c0002t0001g0165 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-121-6410T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69555770 | ||||||
| chr12:69556008
|
C | CG | 46 | a0001c0001t0002g0208a0001c0001t0002g0271a0001c0001t0002g0282others(43): Show | 46 | HG00140.hp2 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.-121-6161dupG | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69556008 | |||||
| chr12:69556008
|
C | CGG | 26 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(23): Show | 26 | HG00140.hp1 HG00408.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.-121-6162_-121-616 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69556008 | |||||
| chr12:69556008
|
CG | C | 105 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0266others(102): Show | 106 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.-121-6161delG | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69556008 | |||||
| chr12:69556008
|
CGG | C | 103 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(100): Show | 103 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.-121-6162_-121-616 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69556008 | |||||
| chr12:69556019
|
G | T | 4 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(1): Show | 4 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121-6161G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556019 | ||||||
| chr12:69556020
|
C | T | 4 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(1): Show | 4 | HG01069.hp1 HG01361.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121-6160C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556020 | ||||||
| chr12:69556120
|
C | T | 3 | a0001c0002t0001g0197a0001c0002t0001g0198a0001c0002t0001g0199 | 3 | HG01884.hp2 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-121-6060C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556120 | ||||||
| chr12:69556249
|
T | G | 1 | a0001c0002t0001g0262 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-121-5931T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556249 | ||||||
| chr12:69556325
|
T | TTTTC | 71 | a0001c0001t0013g0189a0001c0001t0013g0190a0001c0001t0013g0191others(68): Show | 71 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-121-5835_-121-583 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69556325 | |||||
| chr12:69556407
|
A | G | 1 | a0001c0002t0001g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-121-5773A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556407 | ||||||
| chr12:69556463
|
G | T | 1 | a0001c0002t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-121-5717G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556463 | ||||||
| chr12:69556464
|
C | T | 1 | a0001c0002t0001g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-121-5716C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556464 | ||||||
| chr12:69556602
|
G | A | 1 | a0001c0002t0006g0261 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-121-5578G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556602 | ||||||
| chr12:69556765
|
C | T | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-121-5415C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556765 | ||||||
| chr12:69556805
|
T | A | 1 | a0001c0002t0001g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-121-5375T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556805 | ||||||
| chr12:69556855
|
A | G | 9 | a0001c0002t0001g0120a0001c0002t0007g0113a0001c0002t0007g0119others(6): Show | 9 | HG00741.hp2 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-121-5325A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69556855 | ||||||
| chr12:69557357
|
G | C | 1 | a0001c0001t0002g0272 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-121-4823G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557357 | ||||||
| chr12:69557492
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-121-4688T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557492 | ||||||
| chr12:69557593
|
A | ATT | 14 | a0001c0002t0001g0108a0001c0002t0001g0124a0001c0002t0001g0128others(11): Show | 14 | HG00558.hp2 HG00597.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.-121-4586_-121-458 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557593 | |||||
| chr12:69557594
|
T | TGTGTGTG others(10): Show |
1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-121-4586_-121-458 others(21): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557594 | ||||||
| chr12:69557594
|
T | TTGTGTGT others(1): Show |
6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0309others(3): Show | 6 | HG00597.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-121-4567_-121-456 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
T | TTGTGTGT others(3): Show |
13 | a0001c0001t0002g0287a0001c0001t0002g0291a0001c0001t0002g0292others(10): Show | 13 | HG01106.hp2 HG02055.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.-121-4569_-121-456 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
T | TTGTGTGT others(5): Show |
14 | a0001c0001t0002g0273a0001c0001t0002g0290a0001c0001t0002g0295others(11): Show | 15 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-121-4571_-121-456 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
T | TTGTGTGT others(7): Show |
6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-121-4574_-121-457 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0020g0224a0001c0001t0020g0225 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-121-4574_-121-457 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
T | TTGTGTGT others(7): Show |
8 | a0001c0001t0002g0274a0001c0001t0002g0285a0001c0001t0002g0293others(5): Show | 8 | HG01978.hp2 HG03516.hp1 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-121-4573_-121-456 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0002g0283a0001c0001t0029g0206 | 2 | HG01069.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-121-4575_-121-456 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0014g0008 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-121-4577_-121-456 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
T | TTGTGTGT others(17): Show |
2 | a0001c0001t0014g0009a0001c0001t0014g0010 | 2 | HG01167.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-121-4583_-121-456 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
T | TTTTGTG | 3 | a0001c0002t0001g0159a0001c0002t0001g0188a0001c0002t0001g0218 | 3 | HG01358.hp1 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-121-4585_-121-458 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
T | TTTTGTGT others(3): Show |
2 | a0001c0001t0030g0201a0001c0002t0011g0112 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-121-4585_-121-458 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
TTG | T | 28 | a0001c0001t0003g0019a0001c0001t0003g0026a0001c0001t0003g0033others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.-121-4561_-121-456 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557594
|
TTGTG | T | 3 | a0001c0001t0004g0100a0001c0001t0004g0102a0001c0001t0004g0107 | 3 | NA18971.hp2 NA19062.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-121-4563_-121-456 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557594 | |||||
| chr12:69557595
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0001g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-121-4574_-121-457 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557595 | |||||
| chr12:69557596
|
G | T | 89 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(86): Show | 89 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-121-4584G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557596 | ||||||
| chr12:69557615
|
T | C | 1 | a0001c0002t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-121-4565T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557615 | ||||||
| chr12:69557617
|
T | C | 7 | a0001c0001t0003g0024a0001c0001t0003g0027a0001c0001t0004g0090others(4): Show | 7 | HG01516.hp1 HG02132.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-121-4563T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557617 | ||||||
| chr12:69557617
|
T | TGC | 3 | a0001c0001t0003g0021a0001c0001t0003g0221a0001c0001t0003g0222 | 3 | HG01070.hp1 HG01071.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-121-4562_-121-456 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557617 | |||||
| chr12:69557617
|
TGTGCGCG others(5): Show |
T | 1 | a0001c0001t0004g0104 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-121-4561_-121-455 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557617 | |||||
| chr12:69557619
|
T | C | 50 | a0001c0001t0003g0016a0001c0001t0003g0020a0001c0001t0003g0021others(47): Show | 50 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.-121-4561T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557619 | ||||||
| chr12:69557619
|
T | TGC | 8 | a0001c0001t0003g0023a0001c0001t0003g0038a0001c0001t0003g0042others(5): Show | 8 | HG00544.hp1 HG01496.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.-121-4544_-121-454 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGCGCGCG others(1): Show |
4 | a0001c0002t0001g0131a0001c0002t0001g0138a0001c0002t0001g0192others(1): Show | 4 | HG03669.hp2 NA18961.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121-4550_-121-454 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGCGCGCG others(3): Show |
1 | a0001c0002t0001g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-121-4552_-121-454 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGCGC | 4 | a0001c0002t0001g0130a0001c0002t0001g0167a0001c0002t0001g0168others(1): Show | 4 | HG02970.hp2 NA18981.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(10): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGCGCA others(1): Show |
4 | a0001c0001t0013g0190a0001c0002t0001g0179a0001c0002t0001g0215others(1): Show | 4 | HG00733.hp2 HG01361.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGCGCA others(3): Show |
12 | a0001c0001t0013g0191a0001c0001t0026g0145a0001c0002t0001g0117others(9): Show | 12 | HG00408.hp1 HG01070.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGCGCG others(1): Show |
16 | a0001c0002t0001g0122a0001c0002t0001g0126a0001c0002t0001g0127others(13): Show | 16 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGCGCG others(3): Show |
1 | a0001c0002t0001g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGCG others(1): Show |
4 | a0001c0002t0001g0214a0001c0002t0007g0121a0001c0002t0007g0155others(1): Show | 4 | HG00741.hp2 HG02897.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGCG others(5): Show |
1 | a0001c0002t0001g0200 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGCG others(3): Show |
4 | a0001c0002t0001g0140a0001c0002t0001g0162a0001c0002t0001g0178others(1): Show | 4 | HG01258.hp1 NA19003.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGCG others(5): Show |
3 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0216 | 3 | HG00639.hp2 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(3): Show |
1 | a0001c0002t0001g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(5): Show |
8 | a0001c0002t0001g0161a0001c0002t0001g0172a0001c0002t0001g0196others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(7): Show |
1 | a0001c0002t0001g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(9): Show |
1 | a0001c0002t0001g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(5): Show |
5 | a0001c0002t0001g0185a0001c0002t0007g0119a0001c0002t0011g0109others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(7): Show |
3 | a0001c0002t0001g0164a0001c0002t0001g0197a0001c0002t0001g0199 | 3 | HG01346.hp2 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(9): Show |
1 | a0001c0002t0001g0156 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(9): Show |
2 | a0001c0001t0009g0336a0001c0001t0009g0339 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(11): Show |
2 | a0001c0001t0009g0338a0001c0001t0009g0340 | 2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(5): Show |
4 | a0001c0001t0002g0203a0001c0002t0006g0257a0001c0002t0006g0263others(1): Show | 4 | HG01109.hp1 HG03688.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(16): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0002g0320a0001c0001t0002g0322 | 2 | NA19002.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(9): Show |
1 | a0001c0002t0001g0198 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(13): Show |
2 | a0001c0001t0009g0337a0001c0001t0009g0341 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(7): Show |
3 | a0001c0002t0006g0253a0001c0002t0006g0255a0001c0002t0006g0256 | 3 | HG00639.hp1 HG00741.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(18): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(9): Show |
5 | a0001c0001t0002g0272a0001c0001t0002g0284a0001c0001t0002g0330others(2): Show | 5 | HG00609.hp2 HG00673.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(11): Show |
6 | a0001c0001t0002g0271a0001c0001t0002g0286a0001c0001t0002g0289others(3): Show | 6 | HG01934.hp2 HG01952.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(12): Show |
1 | a0001c0001t0002g0270 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(23): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(9): Show |
3 | a0001c0001t0002g0278a0001c0001t0002g0314a0001c0002t0006g0252 | 3 | HG00642.hp2 NA18961.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(20): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(11): Show |
19 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(16): Show | 19 | HG02027.hp1 NA18612.hp1 NA18945.hp2 others(16): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(13): Show |
5 | a0001c0001t0002g0269a0001c0001t0002g0276a0001c0001t0002g0288others(2): Show | 5 | HG02074.hp2 HG02451.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0002g0321 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(13): Show |
3 | a0001c0001t0002g0208a0001c0001t0002g0279a0001c0001t0002g0328 | 3 | NA19007.hp2 NA19063.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(15): Show |
3 | a0001c0001t0002g0305a0001c0001t0027g0268a0001c0002t0001g0123 | 3 | HG02976.hp2 HG03831.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(26): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(13): Show |
1 | a0001c0001t0031g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(15): Show |
1 | a0001c0001t0002g0310 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(26): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(15): Show |
1 | a0001c0001t0002g0306 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-121-4560_-121-455 others(26): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
T | TGTGTGTG others(17): Show |
2 | a0001c0001t0002g0275a0001c0001t0002g0311 | 2 | HG00558.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.-121-4560_-121-455 others(28): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
TGC | T | 3 | a0001c0001t0003g0018a0001c0001t0004g0082a0001c0002t0001g0110 | 3 | HG02071.hp2 HG03239.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-121-4544_-121-454 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557619
|
TGCGCGCG others(13): Show |
T | 1 | a0001c0001t0017g0302 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-121-4559_-121-454 others(24): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557619 | |||||
| chr12:69557620
|
GCGCGCGC others(11): Show |
G | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | HG03041.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-121-4559_-121-454 others(22): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557620 | ||||||
| chr12:69557621
|
C | T | 23 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0273others(20): Show | 23 | HG00597.hp2 HG01256.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-121-4559C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557621 | ||||||
| chr12:69557622
|
G | GTGTGTGT others(6): Show |
1 | a0001c0001t0002g0333 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-121-4558_-121-455 others(17): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557622 | ||||||
| chr12:69557622
|
GCGCGCGC others(15): Show |
G | 1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-121-4557_-121-453 others(26): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557622 | ||||||
| chr12:69557623
|
C | G | 1 | a0001c0001t0002g0333 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-121-4557C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557623 | ||||||
| chr12:69557623
|
C | T | 4 | a0001c0001t0002g0309a0001c0002t0001g0110a0001c0002t0001g0139others(1): Show | 4 | HG00597.hp2 HG01256.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-121-4557C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557623 | ||||||
| chr12:69557625
|
C | T | 4 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0309others(1): Show | 4 | HG00597.hp2 HG01256.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121-4555C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557625 | ||||||
| chr12:69557626
|
G | A | 1 | a0001c0001t0009g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-121-4554G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557626 | ||||||
| chr12:69557627
|
C | T | 4 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0309others(1): Show | 4 | HG00597.hp2 HG01256.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121-4553C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557627 | ||||||
| chr12:69557628
|
G | A | 1 | a0001c0001t0002g0270 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-121-4552G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557628 | ||||||
| chr12:69557628
|
G | GCA | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-121-4551_-121-455 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557628 | |||||
| chr12:69557628
|
G | GCGCA | 12 | a0001c0002t0001g0124a0001c0002t0001g0134a0001c0002t0001g0135others(9): Show | 12 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.-121-4549_-121-454 others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557628 | |||||
| chr12:69557629
|
C | CGCGCTGC others(8): Show |
1 | a0001c0002t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-121-4547_-121-454 others(19): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557629 | |||||
| chr12:69557629
|
C | G | 1 | a0001c0001t0002g0270 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-121-4551C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557629 | ||||||
| chr12:69557629
|
C | T | 2 | a0001c0001t0004g0101a0001c0002t0032g0254 | 2 | HG01256.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-121-4551C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557629 | ||||||
| chr12:69557631
|
C | T | 16 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(13): Show | 16 | HG01069.hp1 HG01109.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.-121-4549C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557631 | ||||||
| chr12:69557632
|
G | GTT | 4 | a0001c0001t0005g0245a0001c0001t0014g0008a0001c0001t0014g0009others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121-4548_-121-454 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557632 | ||||||
| chr12:69557632
|
G | T | 15 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(12): Show | 15 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.-121-4548G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557632 | ||||||
| chr12:69557635
|
CGCAGGTG others(3): Show |
C | 1 | a0001c0002t0032g0254 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-121-4541_-121-453 others(14): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557635 | |||||
| chr12:69557636
|
G | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-121-4544G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557636 | ||||||
| chr12:69557639
|
G | T | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | HG03041.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-121-4541G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557639 | ||||||
| chr12:69557643
|
C | T | 4 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(1): Show | 4 | HG02976.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121-4537C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557643 | ||||||
| chr12:69557644
|
A | G | 5 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG01891.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-121-4536A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557644 | ||||||
| chr12:69557648
|
A | G | 18 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(15): Show | 19 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-121-4532A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557648 | ||||||
| chr12:69557650
|
G | A | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-121-4530G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557650 | ||||||
| chr12:69557693
|
C | T | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-121-4487C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557693 | ||||||
| chr12:69557730
|
T | C | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-121-4450T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557730 | ||||||
| chr12:69557775
|
T | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-121-4405T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557775 | ||||||
| chr12:69557796
|
A | G | 3 | a0001c0002t0001g0140a0001c0002t0001g0178a0001c0002t0001g0214 | 3 | NA18953.hp2 NA19003.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-121-4384A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557796 | ||||||
| chr12:69557988
|
A | ATG | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-121-4180_-121-417 others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69557988 | |||||
| chr12:69557988
|
A | G | 1 | a0001c0001t0003g0040 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-121-4192A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69557988 | ||||||
| chr12:69558099
|
A | G | 1 | a0001c0001t0002g0283 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-121-4081A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69558099 | ||||||
| chr12:69558209
|
G | C | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-121-3971G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69558209 | ||||||
| chr12:69558514
|
C | T | 1 | a0001c0001t0033g0242 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-121-3666C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69558514 | ||||||
| chr12:69558517
|
G | C | 17 | a0001c0001t0002g0275a0001c0001t0002g0277a0001c0001t0002g0304others(14): Show | 17 | HG00558.hp1 HG00609.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.-121-3663G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69558517 | ||||||
| chr12:69558587
|
G | T | 1 | a0001c0002t0001g0262 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-121-3593G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69558587 | ||||||
| chr12:69558693
|
A | G | 1 | a0001c0001t0002g0273 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-121-3487A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69558693 | ||||||
| chr12:69558730
|
G | A | 305 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(302): Show | 306 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.-121-3450G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69558730 | ||||||
| chr12:69558771
|
G | A | 5 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02976.hp1 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121-3409G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69558771 | ||||||
| chr12:69558771
|
G | T | 1 | a0001c0002t0001g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-121-3409G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69558771 | ||||||
| chr12:69558823
|
A | C | 1 | a0001c0002t0001g0171 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-121-3357A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69558823 | ||||||
| chr12:69559463
|
A | G | 18 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(15): Show | 18 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-121-2717A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69559463 | ||||||
| chr12:69559604
|
C | T | 1 | a0001c0001t0002g0325 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-121-2576C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69559604 | ||||||
| chr12:69559709
|
A | G | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-121-2471A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69559709 | ||||||
| chr12:69559787
|
T | TA | 25 | a0001c0001t0002g0333a0001c0001t0003g0017a0001c0001t0003g0018others(22): Show | 25 | HG00544.hp1 HG00673.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.-121-2380dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69559787 | |||||
| chr12:69559816
|
C | T | 2 | a0001c0002t0006g0259a0001c0002t0006g0260 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-121-2364C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69559816 | ||||||
| chr12:69560047
|
T | C | 1 | a0001c0001t0003g0022 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-121-2133T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69560047 | ||||||
| chr12:69560048
|
A | G | 9 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-121-2132A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69560048 | ||||||
| chr12:69560128
|
A | C | 2 | a0001c0001t0020g0224a0001c0001t0020g0225 | 2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-121-2052A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69560128 | ||||||
| chr12:69560263
|
A | G | 2 | a0001c0001t0003g0039a0001c0001t0003g0048 | 2 | HG02074.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-121-1917A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69560263 | ||||||
| chr12:69560266
|
A | C | 3 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | HG03041.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-121-1914A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69560266 | ||||||
| chr12:69560272
|
C | T | 69 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.-121-1908C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69560272 | ||||||
| chr12:69560293
|
G | GT | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-121-1879dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69560293 | |||||
| chr12:69560650
|
T | G | 1 | a0001c0001t0004g0084 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-121-1530T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69560650 | ||||||
| chr12:69560682
|
G | A | 2 | a0001c0001t0008g0005a0001c0001t0008g0006 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-121-1498G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69560682 | ||||||
| chr12:69560789
|
A | G | 1 | a0001c0002t0007g0154 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-121-1391A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69560789 | ||||||
| chr12:69560869
|
A | G | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-121-1311A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69560869 | ||||||
| chr12:69561038
|
C | T | 1 | a0001c0001t0003g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-121-1142C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69561038 | ||||||
| chr12:69561078
|
T | C | 79 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(76): Show | 79 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.-121-1102T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69561078 | ||||||
| chr12:69561155
|
G | A | 1 | a0001c0001t0017g0302 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-121-1025G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69561155 | ||||||
| chr12:69561287
|
A | G | 18 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(15): Show | 18 | HG01069.hp1 HG01109.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-121-893A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69561287 | ||||||
| chr12:69561294
|
ATTGAAGT others(21): Show |
A | 3 | a0001c0001t0003g0024a0001c0001t0003g0027a0001c0001t0034g0025 | 3 | HG02132.hp2 HG02523.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-121-860_-121-833d others(30): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 69561294 | |||||
| chr12:69561380
|
T | C | 1 | a0001c0001t0005g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-121-800T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69561380 | ||||||
| chr12:69561495
|
T | G | 1 | a0001c0001t0009g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-121-685T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69561495 | ||||||
| chr12:69561540
|
G | C | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-121-640G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69561540 | ||||||
| chr12:69561905
|
T | C | 79 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(76): Show | 79 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.-121-275T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69561905 | ||||||
| chr12:69562013
|
A | G | 1 | a0001c0002t0001g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-121-167A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69562013 | ||||||
| chr12:69562428
|
G | A | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-27+154G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69562428 | ||||||
| chr12:69562695
|
T | A | 2 | a0001c0001t0022g0235a0001c0001t0023g0105 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-27+421T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69562695 | ||||||
| chr12:69562730
|
T | C | 241 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(238): Show | 242 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(239): Show |
intron_variant | MODIFIER | c.-27+456T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69562730 | ||||||
| chr12:69562908
|
T | C | 1 | a0001c0001t0026g0145 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-27+634T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69562908 | ||||||
| chr12:69563239
|
C | A | 7 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27+965C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69563239 | ||||||
| chr12:69563254
|
T | C | 3 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075 | 3 | HG00733.hp1 HG01192.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-27+980T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69563254 | ||||||
| chr12:69563257
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-27+983G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69563257 | ||||||
| chr12:69563264
|
G | A | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-27+990G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69563264 | ||||||
| chr12:69563354
|
G | T | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27+1080G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69563354 | ||||||
| chr12:69563414
|
T | C | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27+1140T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69563414 | ||||||
| chr12:69563675
|
C | T | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-27+1401C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69563675 | ||||||
| chr12:69563732
|
T | G | 1 | a0001c0001t0003g0018 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-27+1458T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69563732 | ||||||
| chr12:69563815
|
G | C | 9 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-27+1541G>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69563815 | ||||||
| chr12:69563910
|
C | G | 313 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(310): Show | 314 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.-27+1636C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69563910 | ||||||
| chr12:69564068
|
C | T | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-27+1794C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69564068 | ||||||
| chr12:69564074
|
A | G | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-27+1800A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69564074 | ||||||
| chr12:69564422
|
G | T | 121 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(118): Show | 122 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.-27+2148G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69564422 | ||||||
| chr12:69564503
|
G | T | 126 | a0001c0001t0001g0226a0001c0001t0013g0189a0001c0001t0013g0190others(123): Show | 127 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.-27+2229G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69564503 | ||||||
| chr12:69564825
|
G | A | 77 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0064others(74): Show | 77 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-27+2551G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69564825 | ||||||
| chr12:69564983
|
A | G | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-27+2709A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69564983 | ||||||
| chr12:69565191
|
C | G | 4 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013others(1): Show | 4 | HG01361.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+2917C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69565191 | ||||||
| chr12:69565230
|
A | G | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27+2956A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69565230 | ||||||
| chr12:69565376
|
A | T | 16 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(13): Show | 16 | HG01109.hp2 HG01361.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-27+3102A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69565376 | ||||||
| chr12:69565427
|
G | A | 311 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(308): Show | 312 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.-27+3153G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69565427 | ||||||
| chr12:69565598
|
T | C | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-27+3324T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69565598 | ||||||
| chr12:69565821
|
A | AT | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-3174dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69565821 | |||||
| chr12:69565837
|
G | T | 1 | a0001c0002t0001g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-26-3168G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69565837 | ||||||
| chr12:69565889
|
A | G | 4 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0102others(1): Show | 4 | NA18971.hp2 NA18998.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-3116A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69565889 | ||||||
| chr12:69565982
|
G | GT | 117 | a0001c0001t0001g0226a0001c0001t0004g0082a0001c0001t0004g0091others(114): Show | 117 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.-26-3014dupT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69565982 | |||||
| chr12:69565994
|
A | G | 3 | a0001c0001t0003g0236a0001c0001t0003g0237a0001c0001t0003g0238 | 3 | HG02965.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-26-3011A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69565994 | ||||||
| chr12:69566167
|
C | T | 2 | a0001c0001t0003g0016a0001c0001t0003g0058 | 2 | HG00408.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.-26-2838C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566167 | ||||||
| chr12:69566170
|
C | T | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-26-2835C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566170 | ||||||
| chr12:69566187
|
A | C | 3 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0169 | 3 | HG02970.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-26-2818A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566187 | ||||||
| chr12:69566284
|
A | G | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26-2721A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566284 | ||||||
| chr12:69566391
|
C | T | 1 | a0001c0001t0008g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-26-2614C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566391 | ||||||
| chr12:69566471
|
T | A | 1 | a0001c0001t0022g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-26-2534T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566471 | ||||||
| chr12:69566555
|
C | T | 3 | a0001c0001t0003g0017a0001c0001t0003g0022a0001c0001t0003g0023 | 3 | HG01358.hp2 HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-26-2450C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566555 | ||||||
| chr12:69566594
|
C | T | 7 | a0001c0001t0029g0206a0001c0002t0001g0120a0001c0002t0007g0121others(4): Show | 7 | HG00741.hp2 HG01069.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26-2411C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566594 | ||||||
| chr12:69566616
|
TA | T | 231 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(228): Show | 232 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(229): Show |
intron_variant | MODIFIER | c.-26-2378delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69566616 | |||||
| chr12:69566671
|
T | C | 1 | a0001c0001t0025g0013 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-26-2334T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566671 | ||||||
| chr12:69566680
|
C | A | 1 | a0001c0001t0028g0011 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-26-2325C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566680 | ||||||
| chr12:69566686
|
T | G | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26-2319T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566686 | ||||||
| chr12:69566830
|
C | T | 1 | a0001c0002t0001g0188 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-26-2175C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566830 | ||||||
| chr12:69566889
|
C | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-26-2116C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69566889 | ||||||
| chr12:69567162
|
A | ATC | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26-1829_-26-1828d others(4): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69567162 | |||||
| chr12:69567162
|
ATC | A | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-1829_-26-1828d others(4): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69567162 | |||||
| chr12:69567271
|
T | C | 16 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0005g0239others(13): Show | 16 | HG01109.hp2 HG01361.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-26-1734T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69567271 | ||||||
| chr12:69567752
|
G | A | 65 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(62): Show | 65 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.-26-1253G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69567752 | ||||||
| chr12:69567867
|
TAGAC | T | 8 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-1135_-26-1132d others(6): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69567867 | |||||
| chr12:69568264
|
G | A | 229 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(226): Show | 230 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(227): Show |
intron_variant | MODIFIER | c.-26-741G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69568264 | ||||||
| chr12:69568447
|
G | A | 1 | a0001c0001t0004g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-26-558G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69568447 | ||||||
| chr12:69568510
|
T | TCTGC | 91 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(88): Show | 91 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-26-471_-26-468dup others(4): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69568510 | |||||
| chr12:69568510
|
T | TCTGCCTG others(1): Show |
9 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(6): Show | 9 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26-475_-26-468dup others(8): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69568510 | |||||
| chr12:69568510
|
TCTGCCTG others(5): Show |
T | 1 | a0001c0002t0001g0215 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-26-479_-26-468del others(12): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69568510 | |||||
| chr12:69568555
|
G | GTC | 5 | a0001c0001t0003g0016a0001c0001t0003g0058a0001c0001t0023g0105others(2): Show | 5 | HG00408.hp2 HG01258.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-432_-26-431dup others(2): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69568555 | |||||
| chr12:69568555
|
GTC | G | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-26-432_-26-431del others(2): Show |
FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69568555 | |||||
| chr12:69568724
|
GT | G | 229 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(226): Show | 230 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(227): Show |
intron_variant | MODIFIER | c.-26-271delT | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 69568724 | |||||
| chr12:69568752
|
G | A | 1 | a0001c0002t0007g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-26-253G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 4/8 | chr12 | 69568752 | ||||||
| chr12:69569201
|
A | G | 1 | a0001c0002t0037g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.66+105A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 5/8 | chr12 | 69569201 | ||||||
| chr12:69569556
|
A | G | 1 | a0001c0001t0003g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.66+460A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 5/8 | chr12 | 69569556 | ||||||
| chr12:69569586
|
C | T | 215 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(212): Show | 215 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(212): Show |
intron_variant | MODIFIER | c.66+490C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 5/8 | chr12 | 69569586 | ||||||
| chr12:69569705
|
G | A | 228 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(225): Show | 229 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(226): Show |
intron_variant | MODIFIER | c.66+609G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 5/8 | chr12 | 69569705 | ||||||
| chr12:69569792
|
C | T | 1 | a0001c0001t0003g0057 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.67-539C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 5/8 | chr12 | 69569792 | ||||||
| chr12:69569859
|
C | G | 9 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(6): Show | 9 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-472C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 5/8 | chr12 | 69569859 | ||||||
| chr12:69570091
|
C | A | 228 | a0001c0001t0001g0226a0001c0001t0002g0203a0001c0001t0002g0204others(225): Show | 229 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(226): Show |
intron_variant | MODIFIER | c.67-240C>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 5/8 | chr12 | 69570091 | ||||||
| chr12:69570110
|
A | T | 1 | a0001c0001t0002g0312 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.67-221A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 5/8 | chr12 | 69570110 | ||||||
| chr12:69570158
|
G | A | 3 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0010 | 3 | HG01167.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67-173G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 5/8 | chr12 | 69570158 | ||||||
| chr12:69570537
|
T | C | 14 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(11): Show | 14 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.253+20T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 6/8 | chr12 | 69570537 | ||||||
| chr12:69570609
|
G | GA | 6 | a0001c0001t0009g0336a0001c0001t0009g0337a0001c0001t0009g0338others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.253+99dupA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 69570609 | |||||
| chr12:69570674
|
A | G | 3 | a0001c0002t0001g0197a0001c0002t0001g0198a0001c0002t0001g0199 | 3 | HG01884.hp2 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.253+157A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 6/8 | chr12 | 69570674 | ||||||
| chr12:69571230
|
T | G | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.254-46T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 6/8 | chr12 | 69571230 | ||||||
| chr12:69571441
|
A | AC | 4 | a0001c0001t0003g0019a0001c0001t0003g0053a0001c0001t0003g0233others(1): Show | 4 | HG02027.hp2 HG02080.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+11dupC | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 69571441 | |||||
| chr12:69571519
|
A | T | 4 | a0001c0002t0011g0109a0001c0002t0011g0111a0001c0002t0011g0112others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+85A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/8 | chr12 | 69571519 | ||||||
| chr12:69571588
|
G | A | 13 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+154G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/8 | chr12 | 69571588 | ||||||
| chr12:69571598
|
A | G | 3 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097 | 3 | HG01123.hp2 HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.412+164A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/8 | chr12 | 69571598 | ||||||
| chr12:69571757
|
G | A | 1 | a0001c0002t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.412+323G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/8 | chr12 | 69571757 | ||||||
| chr12:69571789
|
G | A | 1 | a0001c0001t0003g0034 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.413-329G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/8 | chr12 | 69571789 | ||||||
| chr12:69571805
|
A | G | 1 | a0001c0001t0004g0102 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.413-313A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/8 | chr12 | 69571805 | ||||||
| chr12:69571828
|
C | T | 1 | a0001c0002t0018g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.413-290C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/8 | chr12 | 69571828 | ||||||
| chr12:69571841
|
G | A | 2 | a0001c0001t0023g0105a0001c0001t0028g0011 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.413-277G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/8 | chr12 | 69571841 | ||||||
| chr12:69571888
|
A | G | 1 | a0001c0001t0003g0032 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.413-230A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 7/8 | chr12 | 69571888 | ||||||
| chr12:69572515
|
A | C | 2 | a0001c0002t0007g0119a0001c0002t0007g0211 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.576+234A>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69572515 | ||||||
| chr12:69572618
|
A | G | 1 | a0001c0002t0001g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.576+337A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69572618 | ||||||
| chr12:69572679
|
C | T | 221 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(218): Show | 221 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(218): Show |
intron_variant | MODIFIER | c.576+398C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69572679 | ||||||
| chr12:69572976
|
G | A | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.576+695G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69572976 | ||||||
| chr12:69573084
|
C | T | 2 | a0001c0001t0022g0235a0001c0001t0031g0014 | 2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.576+803C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573084 | ||||||
| chr12:69573153
|
A | G | 9 | a0001c0001t0001g0226a0001c0001t0008g0002a0001c0001t0008g0003others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.577-852A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573153 | ||||||
| chr12:69573256
|
T | C | 3 | a0001c0001t0005g0012a0001c0001t0005g0015a0001c0001t0025g0013 | 3 | HG01361.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.577-749T>C | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573256 | ||||||
| chr12:69573276
|
A | G | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.577-729A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573276 | ||||||
| chr12:69573322
|
C | T | 20 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0005g0012others(17): Show | 20 | HG01109.hp2 HG01167.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.577-683C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573322 | ||||||
| chr12:69573512
|
TA | T | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.577-491delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 69573512 | |||||
| chr12:69573514
|
A | G | 13 | a0001c0002t0006g0001a0001c0002t0006g0252a0001c0002t0006g0253others(10): Show | 14 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.577-491A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573514 | ||||||
| chr12:69573608
|
G | T | 1 | a0001c0002t0001g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.577-397G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573608 | ||||||
| chr12:69573639
|
T | G | 1 | a0001c0001t0026g0145 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.577-366T>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573639 | ||||||
| chr12:69573715
|
A | T | 1 | a0001c0001t0002g0288 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.577-290A>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573715 | ||||||
| chr12:69573856
|
C | T | 307 | a0001c0001t0001g0226a0001c0001t0002g0060a0001c0001t0002g0061others(304): Show | 308 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.577-149C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573856 | ||||||
| chr12:69573918
|
T | A | 5 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-87T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 8/8 | chr12 | 69573918 |