Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MGSCC others(503): Show |
chr12 | 69465388 | 69584793 |
| a0002 | 0/0 | 508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | MGSCC others(503): Show |
chr12 | 69465388 | 69584793 |
| a0003 | 0/0 | 100 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | MGSCC others(95): Show |
chr12 | 69465388 | 69584793 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1524 | 221 | 56 | 27 | 115 | 7 | 14 | FRS2_chr12_69465388_69584793 | FRS2 | ATGGG others(1519): Show |
chr12 | 69465388 | 69584793 | ||
| a0001c0002 | 0/0 | 1524 | 119 | 35 | 27 | 40 | 5 | 12 | FRS2_chr12_69465388_69584793 | FRS2 | ATGGG others(1519): Show |
chr12 | 69465388 | 69584793 | ||
| a0002c0004 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | ATGGG others(1519): Show |
chr12 | 69465388 | 69584793 | ||
| a0003c0003 | 0/0 | 1496 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | ATGGG others(1491): Show |
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 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0002 | 0/0 | 6768 | 72 | 5 | 3 | 62 | 0 | 2 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0003 | 0/0 | 6768 | 66 | 11 | 15 | 30 | 1 | 9 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0004 | 1/0 | 6768 | 24 | 0 | 4 | 15 | 3 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | CAAGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0005 | 0/0 | 6769 | 13 | 12 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6764): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0008 | 0/0 | 6768 | 6 | 6 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAAGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0009 | 0/0 | 6767 | 6 | 6 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0010 | 0/0 | 6768 | 4 | 2 | 1 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAAGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0013 | 0/0 | 6767 | 3 | 0 | 0 | 3 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0014 | 0/0 | 6768 | 3 | 2 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0015 | 0/1 | 6768 | 3 | 1 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0016 | 0/0 | 6768 | 3 | 0 | 0 | 3 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0017 | 0/0 | 6768 | 2 | 2 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0020 | 0/0 | 6768 | 2 | 2 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0022 | 0/0 | 6768 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAAGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0023 | 0/0 | 6768 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAAGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0025 | 0/0 | 6769 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6764): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0026 | 0/0 | 6768 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0027 | 0/0 | 6768 | 1 | 0 | 0 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0028 | 0/0 | 6768 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0029 | 0/0 | 6769 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6764): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0030 | 0/0 | 6768 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0031 | 0/0 | 6769 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6764): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0033 | 0/0 | 6769 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6764): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0034 | 0/0 | 6768 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0035 | 0/0 | 6768 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0001t0036 | 0/0 | 6768 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0001 | 0/0 | 6767 | 84 | 24 | 11 | 37 | 3 | 9 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0006 | 0/0 | 6768 | 13 | 0 | 8 | 0 | 2 | 3 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0007 | 0/0 | 6767 | 8 | 7 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0011 | 0/0 | 6767 | 3 | 3 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0012 | 0/0 | 6767 | 3 | 1 | 2 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAAGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0018 | 0/0 | 6767 | 2 | 0 | 1 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0019 | 0/0 | 6767 | 2 | 0 | 2 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0021 | 0/0 | 6767 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAAGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0024 | 0/0 | 6767 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0032 | 0/0 | 6768 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6763): Show |
chr12 | 69465388 | 69584793 |
| a0001c0002t0037 | 0/0 | 6767 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0002c0004t0011 | 0/0 | 6767 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6762): Show |
chr12 | 69465388 | 69584793 |
| a0003c0003t0002 | 0/0 | 6740 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | CAGGA others(6735): Show |
chr12 | 69465388 | 69584793 |
| actghapid | grch38/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 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0002g0065 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0025 | 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 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0059 | 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 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0004g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0004g0093 | 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 |
| 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 |
| a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0010g0096 | 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 |
| a0001c0001t0013g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0013g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0013g0184 | 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 |
| a0001c0001t0015g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0001t0015g0191 | 0/1 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0016g0064 | 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 |
| a0001c0001t0026g0144 | 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 |
| a0001c0001t0034g0024 | 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 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0147 | 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 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0001g0189 | 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 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 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 |
| a0001c0002t0007g0120 | 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 |
| a0001c0002t0007g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0007g0215 | 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 |
| a0001c0002t0012g0087 | 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 |
| a0001c0002t0018g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| a0001c0002t0019g0141 | 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 |
| a0001c0002t0021g0098 | 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 |
| a0002c0004t0011g0211 | 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 | g0090 | EUR | GBR | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0145 | 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 | g0094 | 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 | g0059 | 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 | g0143 | EAS | CHS | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0123 | 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 | g0212 | 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 | g0038 | 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 | g0141 | 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 | g0146 | 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 | g0120 | 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 | g0095 | 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 | g0189 | 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 | g0214 | 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 | g0086 | 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 | g0088 | 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 | g0019 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0096 | AFR | ACB | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01928 | hp2 | a0001 | c0002 | t0018 | g0135 | 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 | g0287 | 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 | g0020 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0021 | 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 | g0037 | EAS | KHV | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0140 | 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 | g0289 | 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 | g0100 | 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 | g0023 | 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 | g0098 | 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 | g0060 | 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 | g0121 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0093 | AMR | PEL | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0124 | 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 | g0089 | 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 | g0190 | 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 | g0122 | 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 | g0211 | 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 | g0215 | 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 | g0119 | 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 | g0040 | 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 | g0039 | 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 | g0147 | 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 | g0018 | 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 | g0185 | AFR | YRI | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0186 | 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 | g0024 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0288 | 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 | g0022 | 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 | g0136 | 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 | g0153 | 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 | g0138 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0061 | 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 | g0133 | 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 | g0213 | 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 | g0285 | 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 | g0284 | 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 | g0025 | 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 | g0129 | 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 | g0134 | 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 | g0184 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0132 | 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 | g0187 | 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 | g0063 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0102 | 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 | g0036 | 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 | g0305 | 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 | g0131 | 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 | g0148 | 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 | g0306 | 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 | g0307 | 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 | g0103 | 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 | g0188 | 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 | g0062 | 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 | g0101 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19068 | hp2 | a0001 | c0001 | t0016 | g0064 | 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 | g0065 | 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 | g0128 | EAS | JPT | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0130 | 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 | g0126 | 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 | g0058 | 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 | g0139 | 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 | g0127 | 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 | g0087 | 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 | g0144 | 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 | g0085 | 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 | g0137 | 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 | a0001 | c0001 | t0015 | g0191 | REF | REF | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0092 | REF | REF | FRS2_chr12_69465388_69584793 | FRS2 | chr12 | 69465388 | 69584793 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69571314 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69574082 | G | A | 2 | a0001c0002 a0002c0004 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69470390 | A | G | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(30): Show |
301 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(298): 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 | a0001c0001t0013 a0001c0002t0018 a0001c0002t0024 |
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 | a0001c0001t0003 a0001c0001t0034 a0001c0001t0035 others(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 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0025 others(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 | a0001c0001t0005 a0001c0001t0025 a0001c0001t0029 others(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 | a0001c0002t0006 a0001c0002t0032 |
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 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0007 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(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 | a0001c0001t0023 a0001c0001t0028 |
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 | a0001c0002t0006 a0001c0002t0032 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(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 | a0001c0001t0008 a0001c0001t0020 |
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 | a0001c0001t0008 a0001c0001t0020 |
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 | a0001c0002t0011 a0002c0004t0011 |
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 | a0001c0002t0006 a0001c0002t0032 |
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 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(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 | a0001c0002t0006 a0001c0002t0032 |
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 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0017 others(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 | a0001c0001t0008 a0001c0001t0020 |
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 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69470594 | C | T | 6 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0269 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(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 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(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 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 |
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 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0229 others(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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0332 a0001c0001t0002g0333 a0001c0001t0002g0334 others(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 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0003g0223 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | 107 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0013g0148 others(104): Show |
107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-261+1804C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69472334 | |||||||
| chr12:69472430 | C | A | 307 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(304): Show |
308 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(305): 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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(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 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
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 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | a0001c0001t0002g0277 a0001c0001t0002g0328 a0001c0001t0002g0329 others(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 | a0001c0001t0004g0078 a0001c0001t0004g0079 a0001c0001t0004g0080 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0003g0033 a0001c0001t0003g0034 a0001c0001t0003g0035 |
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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | 112 | a0001c0001t0001g0226 a0001c0001t0002g0204 a0001c0001t0002g0205 others(109): Show |
112 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(109): 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 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
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 | 306 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(303): Show |
307 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(304): 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 | 106 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0013g0148 others(103): Show |
106 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(103): 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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0261 others(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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | 130 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(127): Show |
130 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(127): 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 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
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 | a0001c0001t0002g0266 a0001c0001t0003g0017 a0001c0001t0003g0036 others(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 | 220 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(217): Show |
221 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(218): 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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
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 | a0001c0002t0006g0256 a0001c0002t0006g0257 a0001c0002t0006g0258 others(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 | a0001c0001t0004g0078 a0001c0001t0004g0079 a0001c0001t0004g0080 others(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 | 201 | a0001c0001t0001g0226 a0001c0001t0002g0205 a0001c0001t0002g0266 others(198): Show |
202 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(199): 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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0269 others(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 | a0001c0001t0005g0245 a0001c0001t0005g0246 a0001c0001t0005g0247 others(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 | |||||||
| chr12:69477432 | G | A | 10 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0004g0077 a0001c0001t0030g0201 |
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 | a0001c0001t0002g0285 | 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 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 |
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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0003g0028 a0001c0001t0003g0033 a0001c0001t0003g0034 others(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 | a0001c0001t0005g0015 a0001c0001t0009g0336 a0001c0001t0009g0337 others(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 | 181 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(178): Show |
181 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(178): 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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0008g0005 a0001c0001t0008g0006 a0001c0001t0008g0007 |
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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0008g0005 a0001c0001t0008g0006 a0001c0001t0008g0007 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0119 | 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 | 107 | a0001c0001t0001g0226 a0001c0001t0003g0176 a0001c0001t0003g0177 others(104): Show |
107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): 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 | 226 | a0001c0001t0001g0226 a0001c0001t0003g0016 a0001c0001t0003g0017 others(223): Show |
227 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(224): 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 | a0001c0002t0007g0190 | 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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0004g0097 a0001c0001t0010g0094 a0001c0001t0010g0095 others(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 | a0001c0001t0004g0081 a0001c0001t0005g0249 a0001c0001t0005g0250 |
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 | a0001c0001t0005g0239 a0001c0001t0005g0245 a0001c0001t0030g0201 |
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 | a0001c0001t0005g0240 a0001c0001t0005g0241 a0001c0001t0005g0246 others(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 | a0001c0001t0005g0243 a0001c0001t0005g0244 a0001c0001t0033g0242 |
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 | a0001c0002t0021g0098 | 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 | a0001c0001t0003g0017 a0001c0001t0003g0020 a0001c0001t0003g0021 others(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 | 92 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0176 others(89): Show |
92 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(89): 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0301 a0001c0001t0002g0325 a0001c0001t0002g0326 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0002t0007g0120 | 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 | a0001c0001t0017g0302 a0001c0001t0017g0303 |
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 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0103 others(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 | 295 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(292): Show |
296 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(293): 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 | a0001c0001t0003g0029 a0001c0002t0001g0187 |
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 | a0001c0001t0003g0029 a0001c0002t0001g0187 |
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 | a0001c0001t0002g0065 | 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 | a0001c0002t0001g0119 a0001c0002t0011g0109 a0001c0002t0011g0111 others(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 | a0001c0002t0001g0180 a0001c0002t0001g0217 |
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 | a0001c0001t0005g0012 a0001c0001t0029g0206 |
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 | a0001c0002t0001g0119 | 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 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(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 | a0001c0001t0002g0284 | 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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0002t0001g0172 others(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 | 221 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(218): Show |
221 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(218): Show |
intron_variant | MODIFIER | c.-261+10708C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69481238 | |||||||
| chr12:69481281 | AT | A | 129 | a0001c0001t0001g0226 a0001c0001t0002g0275 a0001c0001t0002g0286 others(126): Show |
129 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(126): 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 | a0001c0001t0003g0176 a0001c0001t0003g0177 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | 114 | a0001c0001t0001g0226 a0001c0001t0002g0272 a0001c0001t0003g0176 others(111): Show |
114 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(111): 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 | a0001c0002t0001g0195 a0001c0002t0001g0196 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0017g0302 a0001c0001t0017g0303 |
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 | a0001c0001t0002g0333 a0001c0001t0003g0076 a0001c0001t0005g0249 others(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 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0002t0001g0127 others(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 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(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 | a0001c0001t0005g0015 a0001c0001t0031g0014 |
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 | 305 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(302): Show |
306 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(303): 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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | 115 | a0001c0001t0001g0226 a0001c0001t0003g0176 a0001c0001t0003g0177 others(112): Show |
115 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(112): 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 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 others(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 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 |
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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0006g0253 a0001c0002t0006g0258 |
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 | a0001c0002t0001g0129 | 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0130 a0001c0002t0001g0192 |
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 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0070 |
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 | a0001c0001t0003g0022 a0001c0001t0003g0029 a0001c0001t0003g0059 others(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 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0032 others(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 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0034 others(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 | a0001c0001t0003g0033 a0001c0001t0003g0037 a0001c0001t0003g0038 others(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 | a0001c0001t0003g0018 a0001c0001t0003g0035 a0001c0001t0003g0036 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0042 a0001c0001t0003g0049 others(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 | a0001c0001t0017g0303 a0001c0002t0007g0190 |
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 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0002t0001g0138 |
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 | a0001c0001t0017g0302 a0001c0002t0001g0167 |
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 | a0001c0002t0001g0131 a0001c0002t0001g0132 |
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 | a0001c0002t0001g0165 a0001c0002t0001g0181 |
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 | a0001c0002t0001g0128 a0001c0002t0001g0187 |
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 | a0001c0001t0003g0026 a0001c0001t0003g0044 a0001c0001t0003g0045 others(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 | a0001c0001t0003g0017 a0001c0001t0003g0232 a0001c0001t0004g0086 others(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 | a0001c0001t0003g0019 a0001c0001t0003g0227 a0001c0001t0003g0233 others(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 | a0001c0001t0014g0009 a0001c0001t0014g0010 a0001c0002t0001g0200 |
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 | a0001c0001t0008g0003 a0001c0001t0008g0004 a0001c0001t0008g0005 others(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 | a0001c0001t0002g0287 a0001c0001t0002g0305 a0001c0001t0002g0306 |
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 | a0001c0001t0002g0307 | 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 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0269 others(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 | a0001c0001t0002g0304 a0001c0001t0002g0322 a0003c0003t0002g0324 |
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 | a0001c0001t0002g0285 | 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 | a0001c0001t0002g0288 a0001c0001t0002g0327 |
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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
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 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(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 | a0001c0001t0002g0280 a0001c0001t0002g0281 |
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 | a0001c0001t0002g0289 | 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 | a0001c0001t0002g0301 a0001c0001t0003g0236 a0001c0001t0003g0237 others(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 | a0001c0001t0005g0247 a0001c0001t0005g0248 |
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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0001t0005g0015 a0001c0001t0031g0014 |
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 | a0001c0002t0001g0125 a0001c0002t0001g0129 a0001c0002t0001g0133 |
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 | a0001c0002t0001g0134 a0001c0002t0001g0173 a0001c0002t0001g0197 |
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 | a0001c0002t0001g0136 a0001c0002t0001g0137 a0001c0002t0001g0180 others(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 | a0001c0002t0001g0114 a0001c0002t0001g0126 a0001c0002t0001g0130 others(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 | a0001c0001t0026g0144 a0001c0002t0001g0108 a0001c0002t0001g0143 others(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 | a0001c0001t0023g0105 a0001c0002t0001g0110 a0001c0002t0001g0122 others(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 | a0001c0001t0013g0148 a0001c0001t0013g0184 a0001c0002t0001g0121 others(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 |
9 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0013g0153 others(6): Show |
9 | HG02257.hp2 HG02486.hp1 HG03130.hp1 others(6): 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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0341 others(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 | a0001c0001t0009g0338 a0001c0001t0009g0339 a0001c0002t0001g0159 others(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 | a0001c0001t0020g0224 a0001c0002t0001g0118 a0001c0002t0001g0251 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(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 | 228 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(225): Show |
228 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(225): 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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0002t0001g0159 a0001c0002t0001g0164 a0001c0002t0001g0182 others(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 | 227 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(224): Show |
227 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(224): 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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | 93 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0013g0148 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(90): 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 | a0001c0002t0007g0215 | 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 | 112 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0009g0336 others(109): Show |
112 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(109): 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 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 others(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 | 68 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0005g0012 others(65): Show |
69 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(66): 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 | a0001c0001t0026g0144 a0001c0002t0001g0108 a0001c0002t0001g0121 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0272 others(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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0012g0087 | 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 | a0001c0002t0001g0159 a0001c0002t0001g0164 a0001c0002t0001g0182 others(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 | 228 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(225): Show |
228 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(225): 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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | 242 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(239): Show |
243 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(240): 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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | a0001c0002t0001g0119 a0001c0002t0011g0109 a0001c0002t0011g0111 others(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 | 304 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(301): Show |
305 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(302): 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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | 307 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(304): Show |
308 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(305): 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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 others(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 | a0001c0001t0002g0306 | 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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(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 | a0001c0002t0001g0134 a0001c0002t0001g0212 |
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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(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 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0003g0238 a0001c0001t0005g0240 a0001c0001t0008g0005 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0001t0025g0013 a0001c0002t0001g0262 a0001c0002t0006g0001 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0208 others(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 | 104 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0013g0148 others(101): Show |
104 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-261+19475C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69490005 | |||||||
| chr12:69490141 | G | T | 305 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(302): Show |
306 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(303): 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 | 220 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(217): Show |
221 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(218): 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 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0022g0235 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0002t0007g0190 | 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 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0229 others(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 | 232 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(229): Show |
233 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(230): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | 90 | a0001c0001t0001g0226 a0001c0001t0003g0177 a0001c0001t0008g0005 others(87): Show |
90 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(87): 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 | a0001c0001t0026g0144 a0001c0001t0030g0201 a0001c0002t0001g0114 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0208 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0002t0001g0119 a0001c0002t0011g0109 a0001c0002t0011g0111 others(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 | a0001c0001t0002g0307 | 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 | 111 | a0001c0001t0001g0226 a0001c0001t0003g0176 a0001c0001t0003g0177 others(108): Show |
111 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(108): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0288 | 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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0034g0024 | 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 | a0001c0001t0003g0019 | 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 | a0001c0002t0011g0109 a0001c0002t0011g0111 a0001c0002t0011g0112 others(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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0005g0240 a0001c0001t0005g0243 a0001c0001t0005g0244 others(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 | a0001c0001t0023g0105 a0001c0002t0001g0172 a0001c0002t0001g0220 |
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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0016g0063 a0001c0001t0016g0064 a0001c0001t0016g0066 |
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 | a0001c0002t0001g0172 a0001c0002t0001g0220 |
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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(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 | 242 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(239): Show |
243 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(240): Show |
intron_variant | MODIFIER | c.-261+23087T>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69493617 | |||||||
| chr12:69494037 | G | A | 114 | a0001c0001t0001g0226 a0001c0001t0003g0176 a0001c0001t0003g0177 others(111): Show |
114 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.-261+23507G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494037 | |||||||
| chr12:69494350 | C | G | 242 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(239): Show |
243 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(240): Show |
intron_variant | MODIFIER | c.-261+23820C>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69494350 | |||||||
| chr12:69494367 | T | C | 242 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(239): Show |
243 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(240): 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 | a0001c0001t0003g0026 a0001c0001t0003g0030 a0001c0001t0003g0031 others(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 | a0001c0002t0001g0147 | 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 | a0001c0001t0003g0016 a0001c0001t0003g0059 |
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 | a0001c0002t0001g0110 a0001c0002t0001g0114 a0001c0002t0001g0234 |
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 | 307 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(304): Show |
308 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(305): 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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(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 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0002t0001g0127 others(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 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0199 |
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 | a0001c0001t0002g0308 a0001c0001t0002g0318 a0001c0001t0002g0319 others(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 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
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 | 116 | a0001c0001t0001g0226 a0001c0001t0003g0176 a0001c0001t0003g0177 others(113): Show |
116 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(113): 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 | 116 | a0001c0001t0001g0226 a0001c0001t0003g0176 a0001c0001t0003g0177 others(113): Show |
116 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(113): 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 | a0001c0002t0001g0182 a0001c0002t0001g0186 |
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 | a0001c0001t0003g0228 a0001c0002t0001g0197 a0001c0002t0001g0198 others(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 | a0001c0002t0006g0259 a0001c0002t0006g0260 |
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 | a0001c0001t0003g0051 a0001c0001t0036g0046 |
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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0002t0001g0134 | 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 | 91 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0013g0148 others(88): Show |
91 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(88): 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 | a0001c0002t0001g0136 a0001c0002t0001g0150 |
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 | a0001c0001t0003g0023 | 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 | a0001c0001t0017g0302 a0001c0001t0017g0303 |
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 | 232 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(229): Show |
233 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(230): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 111 | a0001c0001t0001g0226 a0001c0001t0003g0176 a0001c0001t0003g0177 others(108): Show |
111 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(108): 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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | 232 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(229): Show |
233 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(230): 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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | 218 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(215): Show |
218 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(215): 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 | a0001c0002t0001g0130 a0001c0002t0001g0180 |
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 | a0001c0001t0003g0028 a0001c0001t0003g0230 a0001c0001t0028g0011 others(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 | a0001c0001t0023g0105 a0001c0002t0001g0262 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0315 a0001c0002t0006g0261 |
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 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0270 others(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 |
25 | a0001c0001t0002g0273 a0001c0001t0002g0281 a0001c0001t0002g0282 others(22): Show |
25 | HG00544.hp2 HG01346.hp2 HG01884.hp1 others(22): 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 | a0001c0001t0002g0269 a0001c0001t0002g0280 a0001c0001t0002g0310 others(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 | a0001c0001t0002g0309 a0001c0001t0008g0005 a0001c0001t0008g0006 others(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 | a0001c0001t0002g0267 a0001c0002t0001g0117 a0001c0002t0001g0127 others(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 | a0001c0002t0001g0110 a0001c0002t0001g0121 a0001c0002t0001g0131 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0266 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0287 a0001c0001t0002g0321 |
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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | 145 | a0001c0001t0001g0226 a0001c0001t0003g0176 a0001c0001t0003g0177 others(142): Show |
145 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(142): 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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | 114 | a0001c0001t0001g0226 a0001c0001t0003g0176 a0001c0001t0003g0177 others(111): Show |
114 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(111): 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 | a0001c0001t0004g0097 | 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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0004g0078 a0001c0001t0004g0079 a0001c0001t0004g0080 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0002t0007g0120 a0001c0002t0007g0154 a0001c0002t0007g0155 others(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 | a0001c0001t0002g0308 a0001c0001t0002g0314 a0001c0001t0002g0318 others(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 | a0001c0001t0003g0019 | 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 | a0001c0001t0005g0240 a0001c0001t0005g0243 a0001c0001t0005g0244 others(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 | 2 | a0001c0002t0001g0149 a0001c0002t0001g0179 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-260-29851G>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69501014 | |||||||
| chr12:69501172 | TA | T | 231 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(228): Show |
232 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(229): 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 | a0001c0002t0018g0135 | 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0004g0088 a0001c0001t0004g0209 |
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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | 111 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0009g0336 others(108): Show |
111 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(108): 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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0023g0105 a0001c0002t0001g0172 a0001c0002t0001g0220 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0001t0026g0144 | 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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | 107 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0013g0148 others(104): Show |
107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): 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 | a0001c0001t0003g0023 a0001c0001t0003g0027 a0001c0001t0034g0024 |
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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | 105 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0013g0148 others(102): Show |
105 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(102): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0001g0182 a0001c0002t0001g0186 |
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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | 219 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(216): Show |
219 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(216): 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 | a0001c0002t0007g0120 | 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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | 232 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(229): Show |
233 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(230): 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 | a0001c0002t0001g0131 a0001c0002t0001g0132 a0001c0002t0001g0183 |
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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0010g0096 | 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 | a0001c0001t0017g0302 a0001c0001t0017g0303 |
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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0280 a0001c0001t0002g0281 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0203 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0065 a0001c0001t0002g0208 others(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 | a0001c0002t0001g0172 a0001c0002t0001g0220 |
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 | a0001c0002t0001g0159 a0001c0002t0001g0164 a0001c0002t0001g0182 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0004g0090 | 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 | a0001c0001t0003g0039 | 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 | a0001c0001t0003g0018 | 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0004g0097 | 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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | 117 | a0001c0001t0001g0226 a0001c0001t0003g0176 a0001c0001t0003g0177 others(114): Show |
117 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(114): 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 | a0001c0002t0001g0117 a0001c0002t0001g0118 a0001c0002t0001g0194 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0033 a0001c0001t0003g0034 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0003g0036 a0001c0001t0003g0048 |
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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0036 a0001c0001t0003g0037 others(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 | 307 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(304): Show |
308 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(305): 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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | 237 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(234): Show |
238 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(235): 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | 307 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(304): Show |
308 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.-260-17719A>G | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69513146 | |||||||
| chr12:69513151 | G | GT | 249 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(246): Show |
249 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(246): 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 | a0001c0002t0001g0108 a0001c0002t0001g0123 a0001c0002t0001g0133 others(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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | |||||||
| chr12:69513625 | 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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0001c0002t0001g0193 |
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 | 223 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(220): Show |
224 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(221): 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 | a0001c0002t0001g0160 a0001c0002t0001g0181 |
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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 300 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(297): Show |
301 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(298): 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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0002t0001g0147 | 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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0002g0308 a0001c0001t0002g0314 a0001c0001t0002g0318 others(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 | 242 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(239): Show |
243 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(240): 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 | a0001c0001t0003g0036 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0001t0002g0271 a0001c0001t0002g0276 a0001c0001t0002g0291 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | 28 | a0001c0001t0004g0078 a0001c0001t0004g0079 a0001c0001t0004g0080 others(25): Show |
28 | HG00408.hp1 HG00733.hp2 HG01069.hp1 others(25): 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 | a0001c0001t0002g0326 a0001c0001t0005g0239 a0001c0001t0005g0240 others(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 | a0001c0002t0012g0083 a0001c0002t0012g0087 a0001c0002t0012g0099 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | 88 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 others(85): Show |
88 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(85): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0034g0024 | 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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | 102 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 others(99): Show |
102 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-260-13225delA | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 1/8 | chr12 | 69517639 | |||||||
| chr12:69517643 | C | G | 2 | a0001c0001t0005g0244 a0001c0001t0033g0242 |
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 | a0001c0002t0001g0172 a0001c0002t0001g0220 |
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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0002t0001g0216 a0001c0002t0001g0251 |
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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0033 a0001c0001t0003g0034 others(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 | a0001c0002t0001g0188 | 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 | 109 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(106): Show |
109 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(106): 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 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(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 | a0001c0001t0002g0208 a0001c0001t0003g0016 a0001c0001t0003g0017 others(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 | 34 | a0001c0001t0002g0204 a0001c0001t0002g0275 a0001c0001t0002g0290 others(31): Show |
35 | HG00558.hp1 HG00639.hp1 HG00642.hp2 others(32): 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 | a0001c0001t0009g0340 a0001c0001t0009g0341 |
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 | a0001c0002t0001g0188 | 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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | 108 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(105): Show |
108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): 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 | a0001c0002t0001g0188 | 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 | a0001c0002t0001g0188 | 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 | a0001c0002t0001g0188 | 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 | 102 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 others(99): Show |
102 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(99): 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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0033 a0001c0001t0003g0034 others(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 | 237 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(234): Show |
238 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(235): 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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 others(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 | a0001c0001t0008g0003 a0001c0002t0001g0262 a0001c0002t0006g0001 others(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 | 118 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(115): Show |
118 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(115): 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 | a0001c0002t0001g0108 a0001c0002t0001g0123 a0001c0002t0001g0133 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0002g0273 a0001c0001t0002g0301 a0001c0001t0002g0333 |
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 | 103 | a0001c0001t0002g0299 a0001c0001t0013g0148 a0001c0001t0013g0153 others(100): Show |
103 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(100): 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 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0103 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0002t0007g0113 a0001c0002t0007g0190 a0001c0002t0007g0215 |
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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0001t0003g0019 | 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 | a0001c0002t0001g0159 a0001c0002t0001g0164 a0001c0002t0001g0182 others(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 | 110 | a0001c0001t0002g0299 a0001c0001t0009g0336 a0001c0001t0009g0337 others(107): Show |
110 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(107): 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 | a0001c0001t0002g0061 a0001c0001t0002g0065 a0001c0001t0002g0203 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0316 a0001c0001t0003g0040 others(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 | a0001c0001t0002g0062 a0001c0001t0002g0204 a0001c0001t0002g0307 others(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 | a0001c0001t0003g0075 a0001c0001t0004g0089 a0001c0001t0004g0093 others(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 | a0001c0001t0004g0086 a0001c0001t0004g0091 |
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 | 38 | a0001c0001t0002g0306 a0001c0001t0003g0017 a0001c0001t0003g0018 others(35): Show |
38 | HG00408.hp1 HG00673.hp2 HG01123.hp1 others(35): 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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0271 others(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 | a0001c0001t0005g0239 a0001c0001t0005g0241 a0001c0002t0007g0113 |
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 | a0001c0001t0005g0240 a0001c0001t0005g0243 a0001c0001t0005g0244 others(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 | a0001c0001t0002g0270 a0001c0002t0001g0119 a0001c0002t0001g0127 |
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 | a0001c0001t0002g0281 a0001c0002t0001g0262 a0001c0002t0006g0001 others(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 | a0001c0001t0002g0280 a0001c0001t0002g0282 |
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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0008g0003 a0001c0001t0008g0004 a0001c0001t0008g0005 others(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 | a0001c0002t0001g0160 a0001c0002t0001g0181 |
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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | 104 | a0001c0001t0001g0226 a0001c0001t0002g0299 a0001c0001t0013g0148 others(101): Show |
104 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(101): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0138 | 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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0005g0015 a0001c0001t0025g0013 a0001c0001t0031g0014 |
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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0001g0139 a0001c0002t0001g0178 a0001c0002t0001g0213 |
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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0002t0001g0188 | 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 | a0001c0002t0001g0188 | 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 | 292 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(289): Show |
293 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(290): 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 | a0001c0001t0003g0034 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0002c0004t0011g0211 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0124 |
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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0001g0172 a0001c0002t0001g0220 |
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 | a0001c0002t0001g0172 a0001c0002t0001g0220 |
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 | 108 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(105): Show |
108 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(105): 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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0002t0001g0172 a0001c0002t0001g0220 |
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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0002t0001g0187 | 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 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0003g0019 | 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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0013g0148 a0001c0001t0025g0013 a0001c0002t0001g0119 others(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 | 102 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0288 others(99): Show |
102 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(99): 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 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(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 | a0001c0001t0002g0275 a0001c0001t0002g0278 a0001c0001t0002g0290 others(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 | a0001c0001t0002g0065 a0001c0001t0002g0271 a0001c0001t0002g0277 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0003g0027 others(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 | a0001c0001t0002g0208 a0001c0001t0003g0017 a0001c0001t0003g0020 others(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 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0022 others(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 | a0001c0001t0003g0038 | 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 | a0001c0001t0004g0101 | 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 | a0001c0002t0001g0147 | 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 | 109 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(106): Show |
109 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(106): 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0002t0007g0113 a0001c0002t0007g0190 a0001c0002t0007g0215 |
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 | a0001c0001t0017g0302 a0001c0001t0017g0303 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0003g0040 | 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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0003g0020 | 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | 305 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(302): Show |
306 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(303): 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0285 others(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 | a0001c0002t0001g0172 a0001c0002t0001g0220 |
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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0267 a0001c0001t0002g0280 a0001c0001t0002g0281 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | 220 | a0001c0001t0001g0226 a0001c0001t0003g0016 a0001c0001t0003g0017 others(217): Show |
221 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(218): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0298 others(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 | a0001c0002t0001g0172 a0001c0002t0001g0173 a0001c0002t0001g0174 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0286 a0001c0001t0002g0287 others(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 | a0001c0002t0001g0136 | 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 | a0001c0001t0003g0017 a0001c0001t0003g0020 a0001c0001t0003g0021 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | 102 | a0001c0001t0001g0226 a0001c0001t0013g0148 a0001c0001t0013g0153 others(99): Show |
102 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(99): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0004g0085 a0001c0001t0004g0086 a0001c0001t0004g0093 |
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 | a0001c0002t0001g0147 | 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 | 105 | a0001c0001t0001g0226 a0001c0001t0013g0148 a0001c0001t0013g0153 others(102): Show |
105 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(102): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0280 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0124 |
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 | a0001c0001t0003g0034 a0001c0002t0001g0160 |
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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | 229 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(226): Show |
230 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(227): 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 | a0001c0001t0026g0144 | 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 | 95 | a0001c0001t0001g0226 a0001c0001t0003g0230 a0001c0001t0013g0148 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(92): 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 | a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0003g0023 | 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 | a0001c0001t0003g0176 a0001c0001t0003g0177 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0006g0256 a0001c0002t0006g0257 |
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 | a0001c0001t0004g0082 a0001c0001t0004g0084 a0001c0001t0004g0089 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0002t0001g0138 | 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 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0229 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0019g0141 a0001c0002t0019g0142 |
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 | a0001c0002t0001g0108 a0001c0002t0001g0133 a0001c0002t0001g0140 others(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 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0273 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | 288 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(285): Show |
289 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(286): 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 | a0001c0001t0003g0017 a0001c0001t0003g0020 a0001c0001t0003g0021 others(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 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0002t0001g0127 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0280 others(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 | a0001c0001t0004g0093 | 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 | a0001c0001t0003g0067 a0001c0001t0003g0069 a0001c0001t0003g0236 others(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 | a0001c0002t0001g0132 | 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0280 others(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 | a0001c0001t0005g0012 a0001c0001t0025g0013 |
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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0005g0244 a0001c0002t0001g0108 a0001c0002t0001g0124 others(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 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 others(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 | 24 | a0001c0001t0002g0275 a0001c0001t0003g0067 a0001c0001t0028g0011 others(21): Show |
24 | HG00558.hp1 HG00735.hp2 HG00741.hp2 others(21): 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 | a0001c0001t0002g0274 a0001c0001t0002g0276 a0001c0001t0002g0277 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0269 a0001c0001t0002g0270 others(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 | a0001c0001t0002g0294 a0001c0001t0002g0300 a0001c0001t0002g0320 others(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 | a0001c0001t0003g0057 a0001c0001t0003g0068 a0001c0001t0003g0069 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0130 a0001c0002t0001g0192 |
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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | 17 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 others(14): Show |
17 | HG00408.hp1 HG00733.hp2 HG01070.hp2 others(14): 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 | a0001c0002t0007g0190 a0001c0002t0007g0215 |
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 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0002g0297 others(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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | 201 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(198): Show |
202 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(199): 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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | 237 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(234): Show |
238 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(235): 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0044 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0280 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | 216 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(213): Show |
216 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(213): 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 | a0001c0001t0005g0012 a0001c0001t0029g0206 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | 230 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(227): Show |
231 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(228): 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 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 others(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 | a0001c0002t0001g0119 | 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0004g0100 a0001c0002t0001g0110 a0001c0002t0001g0114 others(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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0009g0338 a0001c0001t0009g0339 a0001c0001t0009g0340 others(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 | a0001c0001t0005g0245 a0001c0001t0009g0336 a0001c0001t0033g0242 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0247 a0001c0001t0005g0248 others(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 | a0001c0002t0001g0108 a0001c0002t0001g0119 |
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 |
6 | a0001c0001t0001g0226 a0001c0001t0005g0246 a0001c0001t0029g0206 others(3): Show |
6 | HG01069.hp1 HG01123.hp1 HG01884.hp2 others(3): 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 | a0001c0002t0001g0117 a0001c0002t0001g0124 a0001c0002t0001g0136 others(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 | a0001c0001t0026g0144 a0001c0001t0031g0014 a0001c0002t0001g0127 others(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 | a0001c0002t0001g0126 a0001c0002t0001g0128 a0001c0002t0001g0151 others(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 | a0001c0001t0013g0184 a0001c0002t0001g0121 a0001c0002t0001g0129 others(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 | a0001c0001t0013g0153 a0001c0002t0001g0118 a0001c0002t0001g0125 others(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 | a0001c0001t0005g0015 a0001c0001t0013g0148 a0001c0001t0025g0013 others(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 | a0001c0002t0001g0134 a0001c0002t0001g0171 a0001c0002t0001g0179 others(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 | a0001c0002t0001g0123 | 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0001t0002g0203 a0001c0001t0002g0271 a0001c0001t0002g0272 others(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 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0269 others(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 | a0001c0001t0002g0270 a0001c0001t0002g0280 a0001c0001t0002g0281 others(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 | a0001c0001t0002g0275 a0001c0001t0002g0310 |
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 | a0001c0001t0008g0003 a0001c0001t0008g0007 |
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 | a0001c0001t0008g0004 a0001c0001t0008g0006 |
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 | a0001c0001t0004g0209 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0002t0001g0129 |
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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0002t0007g0120 a0001c0002t0007g0154 a0001c0002t0007g0155 others(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 | a0001c0001t0002g0307 a0001c0001t0002g0310 |
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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0010g0096 | 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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0002t0001g0108 a0001c0002t0001g0123 a0001c0002t0001g0133 others(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 | a0001c0001t0003g0020 | 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | 106 | a0001c0001t0001g0226 a0001c0001t0013g0148 a0001c0001t0013g0153 others(103): Show |
106 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(103): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0119 a0001c0002t0011g0109 a0001c0002t0011g0111 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0285 | 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 | 230 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(227): Show |
231 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(228): 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 | a0001c0001t0004g0089 | 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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0333 a0001c0001t0003g0019 others(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 | 213 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(210): Show |
214 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(211): 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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | 17 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 others(14): Show |
17 | HG00408.hp1 HG00733.hp2 HG01070.hp2 others(14): 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 |
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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | 338 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(335): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): 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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | 230 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(227): Show |
231 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(228): 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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0002t0007g0113 a0001c0002t0007g0120 a0001c0002t0007g0154 others(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 | a0001c0002t0001g0160 a0001c0002t0001g0181 |
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 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0020 others(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 | a0001c0002t0007g0155 a0001c0002t0007g0166 |
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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0002t0001g0145 | 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 | a0001c0001t0002g0270 a0001c0001t0002g0334 a0001c0001t0002g0335 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0002g0321 a0001c0001t0005g0015 a0001c0001t0005g0247 others(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 | a0001c0001t0002g0289 | 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0121 | 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 | a0001c0001t0002g0306 | 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 | 199 | a0001c0001t0002g0309 a0001c0001t0003g0016 a0001c0001t0003g0017 others(196): Show |
200 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.-122+12698G>A | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69544754 | |||||||
| chr12:69545155 | T | A | 284 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(281): Show |
285 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(282): 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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0003g0019 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0134 a0001c0002t0001g0136 a0001c0002t0001g0150 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0002t0007g0113 a0001c0002t0007g0120 a0001c0002t0007g0154 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0035 a0001c0001t0003g0037 others(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 | a0001c0001t0001g0226 a0001c0001t0003g0033 a0001c0001t0003g0034 others(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 | a0001c0002t0001g0145 a0001c0002t0001g0167 a0001c0002t0001g0168 others(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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0002t0011g0109 a0001c0002t0011g0111 a0001c0002t0011g0112 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0003g0019 | 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 | a0001c0001t0003g0019 | 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | 112 | a0001c0001t0001g0226 a0001c0001t0009g0336 a0001c0001t0009g0337 others(109): Show |
112 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(109): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0280 others(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 | 304 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(301): Show |
305 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(302): 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0314 a0001c0001t0002g0316 a0001c0001t0003g0016 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0204 a0001c0001t0002g0208 a0001c0001t0002g0269 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0266 a0001c0001t0002g0267 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0239 a0001c0001t0005g0241 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0003g0026 a0001c0001t0003g0030 a0001c0001t0003g0031 others(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 | a0001c0002t0001g0156 a0001c0002t0024g0219 |
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 | 107 | a0001c0001t0001g0226 a0001c0001t0009g0336 a0001c0001t0009g0337 others(104): Show |
107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): 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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | 255 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(252): Show |
256 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(253): 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 | 230 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(227): Show |
231 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(228): 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 | a0001c0001t0003g0069 a0001c0001t0005g0239 a0001c0001t0005g0240 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | 230 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(227): Show |
231 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(228): 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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | 216 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(213): Show |
216 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(213): Show |
intron_variant | MODIFIER | c.-121-11039C>T | FRS2 | ENSG00000166225.9 | transcript | ENST00000549921.6 | protein_coding | 3/8 | chr12 | 69551141 | |||||||
| chr12:69551383 | AGT | A | 225 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(222): Show |
226 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(223): 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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0003g0037 a0001c0001t0003g0049 a0001c0001t0003g0072 others(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 | a0001c0002t0001g0262 a0001c0002t0006g0001 a0001c0002t0006g0252 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0124 |
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 | 225 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(222): Show |
226 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(223): 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0003g0018 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0282 a0001c0001t0003g0017 others(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 | a0001c0001t0003g0228 a0001c0001t0003g0229 a0001c0001t0008g0002 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0269 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0124 |
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 | 87 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 others(84): Show |
87 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(84): 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 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0175 others(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 | a0001c0001t0003g0051 a0001c0001t0036g0046 |
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 | a0001c0002t0001g0136 | 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 | a0001c0002t0007g0113 a0001c0002t0007g0120 a0001c0002t0007g0154 others(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 | a0001c0002t0001g0119 | 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 | a0001c0001t0004g0088 | 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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0001t0002g0333 a0001c0002t0001g0262 a0001c0002t0006g0001 others(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 | a0001c0001t0017g0302 a0001c0001t0017g0303 |
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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0001t0003g0037 a0001c0001t0003g0049 a0001c0001t0003g0072 others(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 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 |
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 | 218 | a0001c0001t0001g0226 a0001c0001t0003g0016 a0001c0001t0003g0017 others(215): Show |
219 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(216): 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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0002t0001g0136 a0001c0002t0001g0150 |
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 | 211 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(208): Show |
212 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(209): 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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0008g0005 a0001c0001t0008g0006 a0001c0001t0008g0007 |
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 | a0001c0001t0003g0176 a0001c0001t0003g0177 |
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 | a0001c0002t0001g0131 a0001c0002t0001g0138 a0001c0002t0001g0183 |
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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0005g0012 a0001c0001t0029g0206 |
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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0001t0002g0208 a0001c0001t0002g0271 a0001c0001t0002g0282 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0266 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0199 |
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 | a0001c0001t0013g0148 a0001c0001t0013g0153 a0001c0001t0013g0184 others(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 | a0001c0002t0001g0212 | 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 | a0001c0002t0001g0137 | 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 | a0001c0002t0001g0137 | 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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0002t0001g0119 a0001c0002t0007g0113 a0001c0002t0007g0120 others(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 | a0001c0002t0001g0108 a0001c0002t0001g0123 a0001c0002t0001g0127 others(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 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0309 others(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 | a0001c0001t0002g0288 a0001c0001t0002g0291 a0001c0001t0002g0292 others(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 | a0001c0001t0002g0273 a0001c0001t0002g0290 a0001c0001t0002g0295 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
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 | a0001c0001t0002g0274 a0001c0001t0002g0284 a0001c0001t0002g0293 others(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 | a0001c0001t0002g0283 a0001c0001t0029g0206 |
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 | a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0002t0001g0159 a0001c0002t0001g0189 a0001c0002t0001g0218 |
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 | a0001c0001t0030g0201 a0001c0002t0011g0112 |
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 | 27 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0033 others(24): Show |
27 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(24): 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 | a0001c0001t0004g0101 a0001c0001t0004g0103 a0001c0001t0004g0107 |
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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0003g0023 a0001c0001t0003g0027 a0001c0001t0004g0088 others(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 | a0001c0001t0003g0019 a0001c0001t0003g0221 a0001c0001t0003g0222 |
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 | a0001c0001t0003g0016 a0001c0001t0003g0018 a0001c0001t0003g0019 others(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 | a0001c0001t0003g0021 a0001c0001t0003g0040 a0001c0001t0003g0042 others(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 | a0001c0002t0001g0130 a0001c0002t0001g0137 a0001c0002t0001g0192 others(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 | a0001c0002t0001g0129 a0001c0002t0001g0167 a0001c0002t0001g0168 others(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 | a0001c0001t0013g0153 a0001c0002t0001g0179 a0001c0002t0001g0214 others(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 | a0001c0001t0013g0184 a0001c0001t0026g0144 a0001c0002t0001g0117 others(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 | a0001c0002t0001g0121 a0001c0002t0001g0125 a0001c0002t0001g0126 others(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 | a0001c0002t0001g0213 a0001c0002t0007g0120 a0001c0002t0007g0155 others(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 | a0001c0002t0001g0139 a0001c0002t0001g0162 a0001c0002t0001g0178 others(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 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0216 |
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 | a0001c0002t0001g0119 | 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 | a0001c0002t0001g0161 a0001c0002t0001g0172 a0001c0002t0001g0196 others(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 | a0001c0002t0001g0145 | 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 | a0001c0002t0001g0186 a0001c0002t0007g0190 a0001c0002t0011g0109 others(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 | a0001c0002t0001g0164 a0001c0002t0001g0197 a0001c0002t0001g0199 |
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 | a0001c0001t0009g0336 a0001c0001t0009g0339 |
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 | a0001c0001t0009g0338 a0001c0001t0009g0340 |
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 | a0001c0001t0002g0203 a0001c0002t0006g0257 a0001c0002t0006g0263 others(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 | a0001c0001t0002g0320 a0001c0001t0002g0322 |
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 | a0001c0001t0009g0337 a0001c0001t0009g0341 |
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 | a0001c0002t0006g0253 a0001c0002t0006g0255 a0001c0002t0006g0256 |
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 | a0001c0001t0002g0272 a0001c0001t0002g0285 a0001c0001t0002g0330 others(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 | a0001c0001t0002g0271 a0001c0001t0002g0286 a0001c0001t0002g0287 others(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 | a0001c0001t0002g0278 a0001c0001t0002g0314 a0001c0002t0006g0252 |
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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0002g0269 a0001c0001t0002g0276 a0001c0001t0002g0289 others(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 | a0001c0001t0002g0208 a0001c0001t0002g0279 a0001c0001t0002g0328 |
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 | a0001c0001t0002g0307 a0001c0001t0027g0268 a0001c0002t0001g0122 |
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 | a0001c0001t0002g0305 | 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 | a0001c0001t0002g0275 a0001c0001t0002g0311 |
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 | a0001c0001t0003g0022 a0001c0001t0004g0082 a0001c0002t0001g0110 |
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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0273 others(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 | a0001c0001t0002g0309 a0001c0002t0001g0110 a0001c0002t0001g0138 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0309 others(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 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0309 others(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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0002t0001g0123 a0001c0002t0001g0133 a0001c0002t0001g0134 others(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 | a0001c0001t0004g0102 a0001c0002t0032g0254 |
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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0001t0005g0245 a0001c0001t0014g0008 a0001c0001t0014g0009 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
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 | a0001c0002t0001g0139 a0001c0002t0001g0178 a0001c0002t0001g0213 |
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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0001t0003g0039 | 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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0001t0002g0275 a0001c0001t0002g0277 a0001c0001t0002g0304 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0001t0002g0333 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0002t0006g0259 a0001c0002t0006g0260 |
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 | a0001c0001t0003g0020 | 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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0020g0224 a0001c0001t0020g0225 |
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 | a0001c0001t0003g0036 a0001c0001t0003g0048 |
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 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0008g0005 a0001c0001t0008g0006 |
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 | a0001c0001t0003g0040 | 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0001t0003g0023 a0001c0001t0003g0027 a0001c0001t0034g0024 |
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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0001t0022g0235 a0001c0001t0023g0105 |
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 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0001t0026g0144 | 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 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 |
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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0003g0022 | 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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0226 a0001c0001t0013g0148 a0001c0001t0013g0153 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0065 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | 310 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(307): Show |
311 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(308): 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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0103 others(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 | 116 | a0001c0001t0001g0226 a0001c0001t0004g0082 a0001c0001t0004g0091 others(113): Show |
116 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(113): 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 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 |
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 | a0001c0001t0003g0016 a0001c0001t0003g0059 |
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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0002t0001g0167 a0001c0002t0001g0168 a0001c0002t0001g0169 |
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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0003g0017 a0001c0001t0003g0020 a0001c0001t0003g0021 |
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 | a0001c0001t0029g0206 a0001c0002t0001g0119 a0001c0002t0007g0120 others(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 | 230 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(227): Show |
231 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(228): 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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0002t0001g0189 | 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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0005g0239 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(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 | a0001c0001t0002g0203 a0001c0001t0002g0204 a0001c0001t0002g0205 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0001g0214 | 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 | a0001c0001t0003g0016 a0001c0001t0003g0059 a0001c0001t0023g0105 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0001t0001g0226 a0001c0001t0002g0203 a0001c0001t0002g0204 others(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 | a0001c0001t0014g0008 a0001c0001t0014g0009 a0001c0001t0014g0010 |
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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0009g0336 a0001c0001t0009g0337 a0001c0001t0009g0338 others(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 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0199 |
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 | a0001c0001t0008g0002 a0001c0001t0008g0003 a0001c0001t0008g0004 others(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 | a0001c0001t0003g0025 a0001c0001t0003g0053 a0001c0001t0003g0233 others(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 | a0001c0002t0011g0109 a0001c0002t0011g0111 a0001c0002t0011g0112 others(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 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(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 | a0001c0001t0004g0085 a0001c0001t0004g0086 a0001c0001t0004g0093 |
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 | a0001c0001t0004g0103 | 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 | a0001c0001t0023g0105 a0001c0001t0028g0011 |
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 | a0001c0002t0007g0190 a0001c0002t0007g0215 |
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 | a0001c0002t0001g0188 | 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 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0001t0022g0235 a0001c0001t0031g0014 |
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 | a0001c0001t0001g0226 a0001c0001t0008g0002 a0001c0001t0008g0003 others(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 | a0001c0001t0005g0012 a0001c0001t0005g0015 a0001c0001t0025g0013 |
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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0005g0012 others(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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0002t0006g0001 a0001c0002t0006g0252 a0001c0002t0006g0253 others(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 | a0001c0002t0001g0122 | 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 | a0001c0001t0026g0144 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0001g0226 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0002t0001g0195 a0001c0002t0001g0196 a0001c0002t0001g0197 others(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 |