Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10056 |
| ensemblid | ENSG00000116120.11 |
| hgncid | 17800 |
| symbol | FARSB |
| name | phenylalanyl-tRNA synthetase subunit beta |
| refseq_nuc | NM_005687.5 |
| refseq_prot | NP_005678.3 |
| ensembl_nuc | ENST00000281828.8 |
| ensembl_prot | ENSP00000281828.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 222566899 |
| end | 222656092 |
| strand | - |
| ver | v1.2 |
| region | chr2:222566899-222656092 |
| region5000 | chr2:222561899-222661092 |
| regionname0 | FARSB_chr2_222566899_222656092 |
| regionname5000 | FARSB_chr2_222561899_222661092 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 589 | 285 | 46 | 50 | 138 | 12 | 38 | 112 | FARSB_chr2_222561899_222661092 | FARSB | MPTVS others(584): Show |
chr2 | 222561899 | 222661092 |
| a0002 | 1/0 | 589 | 56 | 37 | 9 | 4 | 0 | 5 | 2 | FARSB_chr2_222561899_222661092 | FARSB | MPTVS others(584): Show |
chr2 | 222561899 | 222661092 |
| a0003 | 0/0 | 589 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | MPTVS others(584): Show |
chr2 | 222561899 | 222661092 |
| a0004 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | MPTVS others(584): Show |
chr2 | 222561899 | 222661092 |
| a0005 | 0/0 | 589 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | MPTVS others(584): Show |
chr2 | 222561899 | 222661092 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1767 | 283 | 46 | 50 | 137 | 12 | 37 | FARSB_chr2_222561899_222661092 | FARSB | ATGCC others(1762): Show |
chr2 | 222561899 | 222661092 | ||
| a0001c0004 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | ATGCC others(1762): Show |
chr2 | 222561899 | 222661092 | ||
| a0001c0007 | 0/0 | 1767 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | ATGCC others(1762): Show |
chr2 | 222561899 | 222661092 | ||
| a0002c0002 | 1/0 | 1767 | 56 | 37 | 9 | 4 | 0 | 5 | FARSB_chr2_222561899_222661092 | FARSB | ATGCC others(1762): Show |
chr2 | 222561899 | 222661092 | ||
| a0003c0006 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | ATGCC others(1762): Show |
chr2 | 222561899 | 222661092 | ||
| a0004c0003 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | ATGCC others(1762): Show |
chr2 | 222561899 | 222661092 | ||
| a0005c0005 | 0/0 | 1767 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | ATGCC others(1762): Show |
chr2 | 222561899 | 222661092 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6761 | 83 | 9 | 13 | 49 | 3 | 9 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0002 | 0/0 | 6761 | 74 | 0 | 10 | 55 | 1 | 8 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0003 | 0/1 | 6769 | 57 | 8 | 13 | 20 | 4 | 11 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6764): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0005 | 0/0 | 6760 | 15 | 10 | 2 | 2 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6755): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0007 | 0/0 | 6761 | 8 | 0 | 4 | 0 | 1 | 3 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0008 | 0/0 | 6770 | 7 | 6 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6765): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0010 | 0/0 | 6760 | 4 | 3 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6755): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0011 | 0/0 | 6761 | 4 | 3 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0012 | 0/0 | 6769 | 3 | 3 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6764): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0013 | 0/0 | 6770 | 2 | 0 | 0 | 0 | 2 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6765): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0014 | 0/0 | 6770 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6765): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0015 | 0/0 | 6769 | 2 | 0 | 2 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6764): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0016 | 0/0 | 6761 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0017 | 0/0 | 6762 | 2 | 0 | 0 | 1 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6757): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0018 | 0/0 | 6761 | 2 | 0 | 0 | 0 | 0 | 2 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0019 | 0/0 | 6761 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0020 | 0/0 | 6761 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0021 | 0/0 | 6769 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6764): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0022 | 0/0 | 6769 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6764): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0023 | 0/0 | 6769 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6764): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0025 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0026 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0027 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6755): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0029 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0030 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0031 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0032 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0033 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0001t0034 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0004t0002 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0001c0007t0002 | 0/0 | 6761 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0002c0002t0004 | 1/0 | 6761 | 35 | 17 | 8 | 4 | 0 | 5 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0002c0002t0006 | 0/0 | 6761 | 14 | 14 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0002c0002t0009 | 0/0 | 6760 | 5 | 5 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6755): Show |
chr2 | 222561899 | 222661092 |
| a0002c0002t0024 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0002c0002t0028 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0003c0006t0035 | 0/0 | 6762 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6757): Show |
chr2 | 222561899 | 222661092 |
| a0004c0003t0004 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| a0005c0005t0001 | 0/0 | 6761 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | GCAGT others(6756): Show |
chr2 | 222561899 | 222661092 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0003g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0010g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0010g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0010g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0011g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0011g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0011g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0011g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0012g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0012g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0013g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0013g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0014g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0014g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0015g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0015g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0016g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0017g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0017g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0018g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0018g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0019g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0019g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0020g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0021g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0022g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0023g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0025g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0026g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0027g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0029g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0030g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0031g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0032g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0033g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0001t0034g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0001c0007t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0009g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0024g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0002c0002t0028g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0003c0006t0035g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0004c0003t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| a0005c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0013 | g0290 | EUR | GBR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0039 | EUR | GBR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00280 | hp1 | a0001 | c0001 | t0013 | g0283 | EUR | FIN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0038 | EUR | FIN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | FIN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0216 | EUR | FIN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00597 | hp2 | a0001 | c0001 | t0033 | g0137 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0302 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00642 | hp1 | a0002 | c0002 | t0004 | g0191 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0154 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00735 | hp1 | a0001 | c0001 | t0007 | g0138 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00735 | hp2 | a0001 | c0001 | t0034 | g0163 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00741 | hp1 | a0002 | c0002 | t0004 | g0197 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01081 | hp1 | a0001 | c0001 | t0015 | g0043 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0134 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01106 | hp2 | a0001 | c0001 | t0031 | g0136 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0301 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01175 | hp1 | a0001 | c0001 | t0022 | g0041 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01192 | hp2 | a0002 | c0002 | t0004 | g0208 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01243 | hp1 | a0002 | c0002 | t0004 | g0198 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01255 | hp2 | a0001 | c0001 | t0015 | g0066 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0087 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01257 | hp1 | a0002 | c0002 | t0028 | g0209 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01261 | hp1 | a0002 | c0002 | t0004 | g0206 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01346 | hp2 | a0002 | c0002 | t0004 | g0202 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01358 | hp1 | a0002 | c0002 | t0004 | g0207 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0318 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01433 | hp2 | a0001 | c0001 | t0032 | g0142 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01515 | hp1 | a0001 | c0001 | t0017 | g0255 | EUR | IBS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0047 | EUR | IBS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01884 | hp1 | a0001 | c0001 | t0014 | g0287 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0305 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01891 | hp1 | a0002 | c0002 | t0006 | g0214 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01928 | hp1 | a0003 | c0006 | t0035 | g0297 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0312 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02015 | hp1 | a0001 | c0001 | t0020 | g0021 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02040 | hp2 | a0001 | c0001 | t0020 | g0021 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02055 | hp1 | a0002 | c0002 | t0004 | g0161 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02074 | hp2 | a0002 | c0002 | t0004 | g0188 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02132 | hp2 | a0002 | c0002 | t0004 | g0013 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02145 | hp1 | a0002 | c0002 | t0006 | g0171 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02145 | hp2 | a0002 | c0002 | t0004 | g0211 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | CDX | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02155 | hp2 | a0001 | c0001 | t0026 | g0243 | EAS | CDX | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0284 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02257 | hp2 | a0001 | c0001 | t0016 | g0186 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02258 | hp1 | a0002 | c0002 | t0009 | g0177 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0299 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02280 | hp2 | a0002 | c0002 | t0006 | g0187 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02293 | hp1 | a0002 | c0002 | t0004 | g0013 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02451 | hp1 | a0002 | c0002 | t0006 | g0175 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0285 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0309 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02602 | hp1 | a0001 | c0001 | t0023 | g0071 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0037 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02622 | hp1 | a0002 | c0002 | t0004 | g0203 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0295 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02630 | hp1 | a0002 | c0002 | t0009 | g0012 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0289 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02647 | hp1 | a0004 | c0003 | t0004 | g0160 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02647 | hp2 | a0002 | c0002 | t0006 | g0176 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0135 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0139 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02698 | hp2 | a0002 | c0002 | t0004 | g0194 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02717 | hp1 | a0002 | c0002 | t0004 | g0015 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02723 | hp1 | a0002 | c0002 | t0004 | g0162 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0300 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02735 | hp2 | a0002 | c0002 | t0004 | g0212 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02738 | hp2 | a0002 | c0002 | t0004 | g0196 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02809 | hp2 | a0002 | c0002 | t0006 | g0213 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02886 | hp1 | a0002 | c0002 | t0006 | g0296 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02886 | hp2 | a0002 | c0002 | t0024 | g0181 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0282 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0313 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02922 | hp1 | a0002 | c0002 | t0009 | g0172 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02922 | hp2 | a0002 | c0002 | t0004 | g0200 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02965 | hp2 | a0002 | c0002 | t0004 | g0192 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02970 | hp2 | a0002 | c0002 | t0006 | g0174 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02976 | hp1 | a0002 | c0002 | t0004 | g0281 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0310 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0286 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0315 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0303 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0291 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03139 | hp2 | a0002 | c0002 | t0004 | g0193 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03195 | hp2 | a0002 | c0002 | t0004 | g0014 | AFR | ESN | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03209 | hp1 | a0002 | c0002 | t0004 | g0205 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03209 | hp2 | a0001 | c0001 | t0012 | g0062 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03225 | hp1 | a0002 | c0002 | t0006 | g0011 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0314 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0304 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03491 | hp1 | a0001 | c0001 | t0018 | g0279 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03492 | hp1 | a0001 | c0001 | t0018 | g0280 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0311 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03540 | hp2 | a0002 | c0002 | t0004 | g0014 | AFR | GWD | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03579 | hp1 | a0002 | c0002 | t0006 | g0182 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03579 | hp2 | a0002 | c0002 | t0009 | g0179 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03710 | hp1 | a0002 | c0002 | t0004 | g0199 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03831 | hp1 | a0001 | c0001 | t0008 | g0072 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03834 | hp1 | a0001 | c0001 | t0007 | g0153 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03927 | hp2 | a0002 | c0002 | t0004 | g0195 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | BEB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG04199 | hp1 | a0005 | c0005 | t0001 | g0133 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG04199 | hp2 | a0001 | c0007 | t0002 | g0144 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0298 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18522 | hp2 | a0002 | c0002 | t0004 | g0201 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18906 | hp1 | a0002 | c0002 | t0006 | g0180 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18942 | hp2 | a0001 | c0001 | t0019 | g0170 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18967 | hp1 | a0001 | c0001 | t0017 | g0183 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18968 | hp2 | a0001 | c0001 | t0019 | g0249 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18974 | hp2 | a0001 | c0001 | t0027 | g0233 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18987 | hp2 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18999 | hp1 | a0001 | c0001 | t0029 | g0272 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19011 | hp1 | a0001 | c0001 | t0030 | g0131 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19030 | hp1 | a0002 | c0002 | t0004 | g0204 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0308 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19043 | hp1 | a0002 | c0002 | t0004 | g0173 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19043 | hp2 | a0002 | c0002 | t0004 | g0015 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19054 | hp1 | a0001 | c0001 | t0025 | g0218 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19070 | hp2 | a0002 | c0002 | t0004 | g0190 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19074 | hp1 | a0001 | c0004 | t0002 | g0100 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA19240 | hp2 | a0002 | c0002 | t0004 | g0210 | AFR | YRI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ASW | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0288 | AFR | ASW | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0081 | EUR | TSI | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | GIH | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA20905 | hp2 | a0001 | c0001 | t0021 | g0040 | SAS | GIH | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02109 | hp1 | a0002 | c0002 | t0006 | g0178 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0307 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02486 | hp1 | a0002 | c0002 | t0009 | g0012 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03471 | hp1 | a0002 | c0002 | t0006 | g0011 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0022 | AFR | MSL | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | USA | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| HG06807 | hp2 | a0001 | c0001 | t0016 | g0185 | AFR | USA | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA18955 | hp2 | a0002 | c0002 | t0004 | g0189 | EAS | JPT | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| NA21309 | hp2 | a0001 | c0001 | t0012 | g0063 | AFR | LWK | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0164 | REF | REF | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0004 | g0223 | REF | REF | FARSB_chr2_222561899_222661092 | FARSB | chr2 | 222561899 | 222661092 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222571888 | C | T | 3 | a0001 a0003 a0005 |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
missense_variant | MODERATE | c.1753G>A | p.Val585Ile | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1772/6761 | 1753/1770 | 585/589 | chr2 | 222571888 | |||
| chr2:222613814 | T | C | 1 | a0005 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.1459A>G | p.Thr487Ala | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/17 | 1478/6761 | 1459/1770 | 487/589 | chr2 | 222613814 | |||
| chr2:222639607 | T | C | 1 | a0003 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.428A>G | p.Gln143Arg | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/17 | 447/6761 | 428/1770 | 143/589 | chr2 | 222639607 | |||
| chr2:222639655 | C | T | 1 | a0004 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.380G>A | p.Arg127His | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/17 | 399/6761 | 380/1770 | 127/589 | chr2 | 222639655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222572000 | T | G | 1 | a0001c0004 | 1 | NA19074.hp1 | synonymous_variant | LOW | c.1641A>C | p.Arg547Arg | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1660/6761 | 1641/1770 | 547/589 | chr2 | 222572000 | |||
| chr2:222623700 | G | T | 1 | a0003c0006 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.1201C>A | p.Arg401Arg | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/17 | 1220/6761 | 1201/1770 | 401/589 | chr2 | 222623700 | |||
| chr2:222642852 | T | G | 1 | a0001c0007 | 1 | HG04199.hp2 | splice_region_variant&synonymous_variant | LOW | c.268A>C | p.Arg90Arg | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/17 | 287/6761 | 268/1770 | 90/589 | chr2 | 222642852 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222567060 | T | A | 1 | a0001c0001t0032 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4811A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4811 | chr2 | 222567060 | ||||||
| chr2:222567181 | A | G | 1 | a0001c0001t0026 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4690T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4690 | chr2 | 222567181 | ||||||
| chr2:222567303 | A | C | 1 | a0001c0001t0015 | 2 | HG01081.hp1 HG01255.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4568T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4568 | chr2 | 222567303 | ||||||
| chr2:222567378 | T | C | 10 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(7): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*4493A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4493 | chr2 | 222567378 | ||||||
| chr2:222567785 | T | C | 1 | a0001c0001t0023 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4086A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4086 | chr2 | 222567785 | ||||||
| chr2:222567899 | A | G | 1 | a0003c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3972T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3972 | chr2 | 222567899 | ||||||
| chr2:222567957 | A | C | 1 | a0003c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3914T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3914 | chr2 | 222567957 | ||||||
| chr2:222568110 | AC | A | 2 | a0001c0001t0005 a0001c0001t0010 |
19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3760delG | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3760 | chr2 | 222568110 | ||||||
| chr2:222568160 | A | T | 1 | a0001c0001t0018 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3711T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3711 | chr2 | 222568160 | ||||||
| chr2:222568233 | GT | G | 2 | a0001c0001t0027 a0002c0002t0009 |
6 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3637delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3637 | chr2 | 222568233 | ||||||
| chr2:222568248 | T | C | 5 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0015 others(2): Show |
63 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3623A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3623 | chr2 | 222568248 | ||||||
| chr2:222568277 | C | T | 1 | a0003c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3594G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3594 | chr2 | 222568277 | ||||||
| chr2:222568325 | T | C | 1 | a0003c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3546A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3546 | chr2 | 222568325 | ||||||
| chr2:222568329 | G | A | 1 | a0001c0001t0020 | 2 | HG02015.hp1 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3542C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3542 | chr2 | 222568329 | ||||||
| chr2:222568442 | C | T | 10 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(7): Show |
86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3429G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3429 | chr2 | 222568442 | ||||||
| chr2:222568843 | A | C | 1 | a0001c0001t0010 | 4 | HG00639.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3028T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 3028 | chr2 | 222568843 | ||||||
| chr2:222568986 | G | T | 1 | a0001c0001t0021 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2885C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 2885 | chr2 | 222568986 | ||||||
| chr2:222568989 | G | T | 1 | a0003c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2882C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 2882 | chr2 | 222568989 | ||||||
| chr2:222569096 | G | C | 1 | a0001c0001t0012 | 3 | HG02615.hp1 HG03209.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2775C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 2775 | chr2 | 222569096 | ||||||
| chr2:222569639 | A | G | 1 | a0001c0001t0025 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2232T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 2232 | chr2 | 222569639 | ||||||
| chr2:222569871 | G | A | 1 | a0002c0002t0028 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2000C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 2000 | chr2 | 222569871 | ||||||
| chr2:222569932 | G | A | 1 | a0001c0001t0019 | 2 | NA18942.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1939C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1939 | chr2 | 222569932 | ||||||
| chr2:222570049 | T | C | 3 | a0001c0001t0007 a0001c0001t0031 a0001c0001t0033 |
10 | HG00280.hp2 HG00597.hp2 HG00642.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1822A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1822 | chr2 | 222570049 | ||||||
| chr2:222570101 | T | C | 1 | a0003c0006t0035 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1770A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1770 | chr2 | 222570101 | ||||||
| chr2:222570296 | G | A | 1 | a0001c0001t0033 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1575C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1575 | chr2 | 222570296 | ||||||
| chr2:222570328 | T | G | 4 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0014 others(1): Show |
12 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1543A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1543 | chr2 | 222570328 | ||||||
| chr2:222570337 | G | A | 10 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0018 others(7): Show |
86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1534C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1534 | chr2 | 222570337 | ||||||
| chr2:222570354 | A | C | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0020 others(6): Show |
99 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1517T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1517 | chr2 | 222570354 | ||||||
| chr2:222570528 | C | CT | 5 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0014 others(2): Show |
14 | HG00140.hp1 HG00280.hp1 HG01515.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1342dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1342 | chr2 | 222570528 | ||||||
| chr2:222570721 | C | T | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(33): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*1150G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1150 | chr2 | 222570721 | ||||||
| chr2:222570723 | A | T | 1 | a0001c0001t0014 | 2 | HG01884.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1148T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1148 | chr2 | 222570723 | ||||||
| chr2:222570799 | A | T | 1 | a0001c0001t0031 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1072T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 1072 | chr2 | 222570799 | ||||||
| chr2:222570932 | C | T | 8 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0020 others(5): Show |
98 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*939G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 939 | chr2 | 222570932 | ||||||
| chr2:222571153 | A | G | 1 | a0002c0002t0024 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*718T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 718 | chr2 | 222571153 | ||||||
| chr2:222571222 | T | A | 1 | a0001c0001t0029 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 649 | chr2 | 222571222 | ||||||
| chr2:222571465 | C | CGAACTCA others(1): Show |
9 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(6): Show |
75 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*398_*405dupATGAGT others(2): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 405 | chr2 | 222571465 | ||||||
| chr2:222571639 | C | T | 1 | a0001c0001t0030 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*232G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 232 | chr2 | 222571639 | ||||||
| chr2:222571683 | C | T | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(20): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*188G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 188 | chr2 | 222571683 | ||||||
| chr2:222571709 | T | C | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0020 others(6): Show |
99 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 162 | chr2 | 222571709 | ||||||
| chr2:222571867 | A | G | 1 | a0001c0001t0013 | 2 | HG00140.hp1 HG00280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 17/17 | 4 | chr2 | 222571867 | ||||||
| chr2:222656078 | T | G | 4 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0011 others(1): Show |
24 | HG00639.hp2 HG01109.hp2 HG01361.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-5A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/17 | 5 | chr2 | 222656078 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222572141 | A | G | 69 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(66): Show |
75 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.1619-119T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572141 | |||||||
| chr2:222572153 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-131G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572153 | |||||||
| chr2:222572437 | A | T | 1 | a0001c0001t0017g0183 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1619-415T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572437 | |||||||
| chr2:222572461 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1619-439T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572461 | |||||||
| chr2:222572625 | A | G | 2 | a0002c0002t0004g0161 a0004c0003t0004g0160 |
2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1619-603T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572625 | |||||||
| chr2:222572644 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1619-622T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222572644 | |||||||
| chr2:222573235 | T | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-1213A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222573235 | |||||||
| chr2:222573460 | C | A | 2 | a0002c0002t0006g0011 a0002c0002t0006g0178 |
3 | HG02109.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1619-1438G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222573460 | |||||||
| chr2:222573789 | C | T | 1 | a0001c0001t0005g0318 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1619-1767G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222573789 | |||||||
| chr2:222574136 | A | G | 1 | a0001c0001t0003g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1619-2114T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574136 | |||||||
| chr2:222574160 | C | CT | 74 | a0001c0001t0001g0140 a0001c0001t0003g0001 a0001c0001t0003g0004 others(71): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1619-2139dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574160 | |||||||
| chr2:222574160 | CT | C | 7 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1619-2139delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574160 | |||||||
| chr2:222574227 | G | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-2205C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574227 | |||||||
| chr2:222574237 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1619-2215A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574237 | |||||||
| chr2:222574952 | G | A | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1619-2930C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574952 | |||||||
| chr2:222574980 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-2958G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222574980 | |||||||
| chr2:222575042 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-3020A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575042 | |||||||
| chr2:222575182 | G | C | 2 | a0002c0002t0006g0295 a0002c0002t0006g0296 |
2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1619-3160C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575182 | |||||||
| chr2:222575222 | T | C | 70 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(67): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1619-3200A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575222 | |||||||
| chr2:222575454 | A | T | 1 | a0001c0001t0003g0044 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1619-3432T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575454 | |||||||
| chr2:222575561 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-3539C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575561 | |||||||
| chr2:222575621 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-3599G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575621 | |||||||
| chr2:222575735 | C | T | 1 | a0002c0002t0004g0195 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1619-3713G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575735 | |||||||
| chr2:222575871 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0147 |
3 | HG01070.hp1 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1619-3849C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575871 | |||||||
| chr2:222575977 | CT | C | 73 | a0001c0001t0001g0141 a0001c0001t0002g0234 a0001c0001t0002g0244 others(70): Show |
79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1619-3956delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575977 | |||||||
| chr2:222575984 | T | C | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1619-3962A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222575984 | |||||||
| chr2:222576001 | A | G | 1 | a0001c0001t0005g0310 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1619-3979T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222576001 | |||||||
| chr2:222576171 | C | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-4149G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222576171 | |||||||
| chr2:222576454 | A | G | 2 | a0001c0001t0005g0318 a0001c0001t0034g0163 |
2 | HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1619-4432T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222576454 | |||||||
| chr2:222576519 | T | A | 11 | a0001c0001t0008g0072 a0001c0001t0008g0282 a0001c0001t0008g0284 others(8): Show |
11 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1619-4497A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222576519 | |||||||
| chr2:222576854 | C | T | 1 | a0002c0002t0006g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1619-4832G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222576854 | |||||||
| chr2:222577324 | T | C | 5 | a0002c0002t0006g0171 a0002c0002t0006g0182 a0002c0002t0006g0187 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619-5302A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577324 | |||||||
| chr2:222577339 | C | T | 3 | a0001c0001t0003g0042 a0001c0001t0003g0070 a0001c0001t0023g0071 |
3 | HG02602.hp1 HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1619-5317G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577339 | |||||||
| chr2:222577581 | G | A | 58 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(55): Show |
64 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1619-5559C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577581 | |||||||
| chr2:222577587 | G | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
98 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1619-5565C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577587 | |||||||
| chr2:222577656 | A | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-5634T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577656 | |||||||
| chr2:222577677 | C | T | 1 | a0001c0001t0002g0242 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1619-5655G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577677 | |||||||
| chr2:222577807 | A | T | 79 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(76): Show |
86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1619-5785T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577807 | |||||||
| chr2:222577896 | T | C | 58 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(55): Show |
64 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1619-5874A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222577896 | |||||||
| chr2:222578071 | T | G | 1 | a0002c0002t0004g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1619-6049A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578071 | |||||||
| chr2:222578180 | G | T | 16 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(13): Show |
18 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1619-6158C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578180 | |||||||
| chr2:222578239 | A | G | 1 | a0001c0001t0015g0043 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1619-6217T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578239 | |||||||
| chr2:222578299 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-6277T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578299 | |||||||
| chr2:222578336 | C | G | 1 | a0001c0001t0001g0009 | 2 | NA18982.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1619-6314G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578336 | |||||||
| chr2:222578470 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1619-6448T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578470 | |||||||
| chr2:222578795 | T | C | 281 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1619-6773A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578795 | |||||||
| chr2:222578842 | CG | C | 79 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(76): Show |
86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1619-6821delC | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578842 | |||||||
| chr2:222578883 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-6861T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222578883 | |||||||
| chr2:222579042 | T | C | 79 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(76): Show |
86 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1619-7020A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579042 | |||||||
| chr2:222579104 | T | TG | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-7083dupC | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579104 | |||||||
| chr2:222579120 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(1): Show |
5 | HG01496.hp1 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619-7098T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579120 | |||||||
| chr2:222579134 | A | G | 1 | a0002c0002t0006g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1619-7112T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579134 | |||||||
| chr2:222579141 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
98 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1619-7119G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579141 | |||||||
| chr2:222579391 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
98 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1619-7369C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579391 | |||||||
| chr2:222579649 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-7627T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579649 | |||||||
| chr2:222579926 | G | A | 5 | a0002c0002t0004g0173 a0002c0002t0004g0193 a0002c0002t0004g0204 others(2): Show |
5 | HG02976.hp1 HG03139.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1619-7904C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579926 | |||||||
| chr2:222579941 | A | G | 2 | a0001c0001t0002g0216 a0001c0001t0002g0237 |
2 | HG00323.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1619-7919T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222579941 | |||||||
| chr2:222580031 | A | T | 281 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1619-8009T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580031 | |||||||
| chr2:222580096 | A | G | 63 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(60): Show |
69 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1619-8074T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580096 | |||||||
| chr2:222580146 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1619-8124T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580146 | |||||||
| chr2:222580201 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-8179G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580201 | |||||||
| chr2:222580297 | A | C | 1 | a0001c0001t0003g0054 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1619-8275T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580297 | |||||||
| chr2:222580494 | C | CA | 12 | a0001c0001t0005g0310 a0001c0001t0005g0311 a0001c0001t0005g0312 others(9): Show |
12 | HG00735.hp2 HG01361.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1619-8473dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580494 | |||||||
| chr2:222580494 | CA | C | 149 | a0001c0001t0001g0101 a0001c0001t0001g0113 a0001c0001t0001g0126 others(146): Show |
163 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.1619-8473delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580494 | |||||||
| chr2:222580514 | T | C | 3 | a0001c0001t0010g0022 a0001c0001t0010g0302 a0001c0001t0010g0303 |
4 | HG00639.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1619-8492A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580514 | |||||||
| chr2:222580523 | A | G | 1 | a0001c0001t0030g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1619-8501T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580523 | |||||||
| chr2:222580663 | C | A | 20 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(17): Show |
21 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1619-8641G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580663 | |||||||
| chr2:222580676 | C | T | 3 | a0002c0002t0006g0011 a0002c0002t0006g0178 a0002c0002t0024g0181 |
4 | HG02109.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1619-8654G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580676 | |||||||
| chr2:222580697 | A | G | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-8675T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580697 | |||||||
| chr2:222580859 | G | A | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1619-8837C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580859 | |||||||
| chr2:222580902 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1619-8880A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580902 | |||||||
| chr2:222580953 | A | T | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1619-8931T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580953 | |||||||
| chr2:222580957 | G | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-8935C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580957 | |||||||
| chr2:222580995 | G | A | 14 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(11): Show |
16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1619-8973C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222580995 | |||||||
| chr2:222581020 | C | T | 22 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(19): Show |
23 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.1619-8998G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581020 | |||||||
| chr2:222581184 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-9162A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581184 | |||||||
| chr2:222581243 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-9221C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581243 | |||||||
| chr2:222581265 | T | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-9243A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581265 | |||||||
| chr2:222581383 | A | G | 1 | a0001c0001t0003g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1619-9361T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581383 | |||||||
| chr2:222581591 | C | G | 1 | a0002c0002t0006g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1619-9569G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581591 | |||||||
| chr2:222581609 | C | T | 1 | a0001c0001t0011g0301 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1619-9587G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581609 | |||||||
| chr2:222581700 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-9678G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581700 | |||||||
| chr2:222581858 | T | C | 6 | a0001c0001t0002g0220 a0001c0001t0002g0226 a0001c0001t0002g0227 others(3): Show |
6 | HG01069.hp1 NA18973.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1619-9836A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222581858 | |||||||
| chr2:222582124 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1619-10102T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582124 | |||||||
| chr2:222582193 | T | G | 1 | a0001c0001t0003g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1619-10171A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582193 | |||||||
| chr2:222582437 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1619-10415T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582437 | |||||||
| chr2:222582488 | C | T | 1 | a0001c0001t0002g0242 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1619-10466G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582488 | |||||||
| chr2:222582562 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1619-10540A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582562 | |||||||
| chr2:222582650 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1619-10628G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582650 | |||||||
| chr2:222582651 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1619-10629C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582651 | |||||||
| chr2:222582732 | T | C | 1 | a0001c0001t0015g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1619-10710A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582732 | |||||||
| chr2:222582835 | G | A | 2 | a0001c0001t0002g0216 a0001c0001t0002g0237 |
2 | HG00323.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1619-10813C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582835 | |||||||
| chr2:222582874 | G | A | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1619-10852C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582874 | |||||||
| chr2:222582930 | G | GA | 5 | a0001c0001t0002g0017 a0001c0001t0002g0215 a0001c0001t0002g0234 others(2): Show |
6 | NA18942.hp2 NA18946.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1619-10909dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222582930 | |||||||
| chr2:222583556 | C | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1619-11534G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583556 | |||||||
| chr2:222583672 | C | G | 2 | a0001c0001t0002g0253 a0001c0001t0002g0257 |
2 | HG01358.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1619-11650G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583672 | |||||||
| chr2:222583729 | G | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-11707C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583729 | |||||||
| chr2:222583733 | G | C | 14 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(11): Show |
16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1619-11711C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583733 | |||||||
| chr2:222583780 | T | C | 70 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(67): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1619-11758A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583780 | |||||||
| chr2:222583874 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-11852G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222583874 | |||||||
| chr2:222584013 | G | A | 4 | a0001c0001t0005g0310 a0001c0001t0010g0022 a0001c0001t0010g0302 others(1): Show |
5 | HG00639.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619-11991C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584013 | |||||||
| chr2:222584231 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1619-12209A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584231 | |||||||
| chr2:222584390 | G | A | 1 | a0002c0002t0006g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1619-12368C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584390 | |||||||
| chr2:222584423 | G | A | 77 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(74): Show |
84 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1619-12401C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584423 | |||||||
| chr2:222584431 | T | C | 5 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(2): Show |
5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1619-12409A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584431 | |||||||
| chr2:222584467 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0114 |
2 | NA18942.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1619-12445C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584467 | |||||||
| chr2:222584526 | C | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1619-12504G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584526 | |||||||
| chr2:222584619 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-12597C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584619 | |||||||
| chr2:222584726 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-12704G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584726 | |||||||
| chr2:222584786 | C | T | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1619-12764G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584786 | |||||||
| chr2:222584819 | G | A | 2 | a0001c0001t0003g0005 a0001c0001t0003g0028 |
3 | HG00609.hp1 HG02155.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1619-12797C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584819 | |||||||
| chr2:222584855 | C | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1619-12833G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584855 | |||||||
| chr2:222584977 | G | A | 1 | a0001c0001t0005g0310 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1619-12955C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222584977 | |||||||
| chr2:222585083 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1619-13061A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585083 | |||||||
| chr2:222585101 | G | A | 1 | a0001c0001t0005g0310 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1619-13079C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585101 | |||||||
| chr2:222585112 | C | T | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1619-13090G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585112 | |||||||
| chr2:222585137 | C | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-13115G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585137 | |||||||
| chr2:222585218 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1619-13196G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585218 | |||||||
| chr2:222585225 | A | G | 1 | a0002c0002t0004g0192 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1619-13203T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585225 | |||||||
| chr2:222585349 | C | A | 1 | a0001c0001t0002g0258 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1619-13327G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585349 | |||||||
| chr2:222585487 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1619-13465G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585487 | |||||||
| chr2:222585488 | G | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-13466C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585488 | |||||||
| chr2:222585624 | G | C | 1 | a0002c0002t0004g0208 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1619-13602C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585624 | |||||||
| chr2:222585754 | G | T | 277 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(274): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1619-13732C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585754 | |||||||
| chr2:222585772 | A | C | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1619-13750T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585772 | |||||||
| chr2:222585882 | G | A | 1 | a0001c0001t0003g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1619-13860C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585882 | |||||||
| chr2:222585925 | G | C | 18 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(15): Show |
19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1619-13903C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585925 | |||||||
| chr2:222585963 | T | C | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1619-13941A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585963 | |||||||
| chr2:222585994 | A | T | 22 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(19): Show |
23 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.1618+13934T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222585994 | |||||||
| chr2:222586146 | A | T | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+13782T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586146 | |||||||
| chr2:222586264 | T | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+13664A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586264 | |||||||
| chr2:222586369 | A | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1618+13559T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586369 | |||||||
| chr2:222586369 | A | T | 3 | a0001c0001t0016g0185 a0001c0001t0016g0186 a0002c0002t0006g0187 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+13559T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586369 | |||||||
| chr2:222586384 | C | T | 2 | a0001c0001t0011g0300 a0001c0001t0011g0301 |
2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1618+13544G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586384 | |||||||
| chr2:222586510 | A | C | 1 | a0001c0001t0008g0288 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1618+13418T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586510 | |||||||
| chr2:222586611 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1618+13317G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586611 | |||||||
| chr2:222586696 | A | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+13232T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586696 | |||||||
| chr2:222586806 | A | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1618+13122T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222586806 | |||||||
| chr2:222587293 | T | C | 3 | a0001c0001t0012g0037 a0001c0001t0012g0062 a0001c0001t0012g0063 |
3 | HG02615.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1618+12635A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587293 | |||||||
| chr2:222587312 | G | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+12616C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587312 | |||||||
| chr2:222587396 | G | C | 1 | a0002c0002t0004g0202 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1618+12532C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587396 | |||||||
| chr2:222587579 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1618+12349A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587579 | |||||||
| chr2:222587600 | T | C | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+12328A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587600 | |||||||
| chr2:222587727 | T | C | 277 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(274): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1618+12201A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587727 | |||||||
| chr2:222587765 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1618+12163C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587765 | |||||||
| chr2:222587842 | G | T | 1 | a0001c0001t0001g0110 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1618+12086C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222587842 | |||||||
| chr2:222588055 | A | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
92 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.1618+11873T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588055 | |||||||
| chr2:222588171 | T | C | 1 | a0002c0002t0006g0178 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1618+11757A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588171 | |||||||
| chr2:222588459 | G | C | 4 | a0001c0001t0002g0246 a0001c0001t0002g0261 a0001c0001t0002g0262 others(1): Show |
4 | HG00597.hp1 NA18957.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+11469C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588459 | |||||||
| chr2:222588550 | A | T | 1 | a0001c0001t0015g0043 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1618+11378T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588550 | |||||||
| chr2:222588630 | C | T | 17 | a0001c0001t0003g0024 a0001c0001t0003g0039 a0001c0001t0003g0047 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.1618+11298G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588630 | |||||||
| chr2:222588710 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1618+11218G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588710 | |||||||
| chr2:222588915 | C | T | 4 | a0002c0002t0009g0012 a0002c0002t0009g0172 a0002c0002t0009g0177 others(1): Show |
5 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+11013G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588915 | |||||||
| chr2:222588926 | C | T | 10 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0025 others(7): Show |
12 | HG00438.hp2 HG00609.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1618+11002G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588926 | |||||||
| chr2:222588980 | T | G | 70 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(67): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1618+10948A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588980 | |||||||
| chr2:222588993 | G | A | 3 | a0001c0001t0012g0037 a0001c0001t0012g0062 a0001c0001t0012g0063 |
3 | HG02615.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1618+10935C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222588993 | |||||||
| chr2:222589080 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0126 |
2 | HG02027.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1618+10848A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589080 | |||||||
| chr2:222589528 | T | TAAAGAGC others(312): Show |
2 | a0002c0002t0006g0295 a0002c0002t0006g0296 |
2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1618+10399_1618+10 others(325): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589528 | |||||||
| chr2:222589528 | T | TAAAGAGC others(313): Show |
8 | a0002c0002t0006g0171 a0002c0002t0006g0174 a0002c0002t0006g0175 others(5): Show |
9 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1618+10399_1618+10 others(326): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589528 | |||||||
| chr2:222589528 | T | TAAAGAGC others(314): Show |
3 | a0002c0002t0006g0011 a0002c0002t0006g0176 a0002c0002t0006g0178 |
4 | HG02109.hp1 HG02647.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1618+10399_1618+10 others(327): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589528 | |||||||
| chr2:222589528 | T | TAAAGAGC others(316): Show |
1 | a0002c0002t0024g0181 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1618+10399_1618+10 others(329): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589528 | |||||||
| chr2:222589656 | C | G | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+10272G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589656 | |||||||
| chr2:222589733 | C | T | 2 | a0001c0001t0005g0314 a0001c0001t0005g0315 |
2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1618+10195G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222589733 | |||||||
| chr2:222590066 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0101 a0001c0001t0001g0122 others(1): Show |
6 | NA18945.hp1 NA18955.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618+9862C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590066 | |||||||
| chr2:222590085 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1618+9843T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590085 | |||||||
| chr2:222590168 | C | T | 6 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(3): Show |
6 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618+9760G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590168 | |||||||
| chr2:222590324 | T | C | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1618+9604A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590324 | |||||||
| chr2:222590363 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+9565G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590363 | |||||||
| chr2:222590369 | G | A | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1618+9559C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590369 | |||||||
| chr2:222590380 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1618+9548C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590380 | |||||||
| chr2:222590513 | T | TA | 18 | a0001c0001t0002g0254 a0001c0001t0005g0304 a0001c0001t0005g0305 others(15): Show |
19 | HG00639.hp2 HG01361.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1618+9414dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590513 | |||||||
| chr2:222590548 | C | CA | 8 | a0001c0001t0003g0026 a0001c0001t0022g0041 a0002c0002t0006g0182 others(5): Show |
9 | HG01175.hp1 HG01928.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1618+9379dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590548 | |||||||
| chr2:222590548 | CA | C | 18 | a0001c0001t0001g0141 a0001c0001t0002g0217 a0001c0001t0008g0282 others(15): Show |
18 | HG00140.hp1 HG00280.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1618+9379delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590548 | |||||||
| chr2:222590548 | CAA | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1618+9378_1618+937 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590548 | |||||||
| chr2:222590628 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+9300A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590628 | |||||||
| chr2:222590645 | G | A | 1 | a0001c0001t0002g0275 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1618+9283C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222590645 | |||||||
| chr2:222591049 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1618+8879A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591049 | |||||||
| chr2:222591122 | A | C | 1 | a0001c0001t0001g0035 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1618+8806T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591122 | |||||||
| chr2:222591158 | G | A | 1 | a0002c0002t0004g0188 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1618+8770C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591158 | |||||||
| chr2:222591211 | T | TA | 105 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
113 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.1618+8716dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591211 | |||||||
| chr2:222591252 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+8676C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591252 | |||||||
| chr2:222591269 | T | G | 1 | a0001c0001t0001g0103 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1618+8659A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591269 | |||||||
| chr2:222591454 | A | G | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+8474T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591454 | |||||||
| chr2:222591461 | A | G | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+8467T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591461 | |||||||
| chr2:222591629 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+8299C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591629 | |||||||
| chr2:222591839 | A | T | 1 | a0001c0001t0029g0272 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1618+8089T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222591839 | |||||||
| chr2:222592017 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+7911C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592017 | |||||||
| chr2:222592133 | T | C | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+7795A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592133 | |||||||
| chr2:222592279 | G | A | 3 | a0001c0001t0016g0185 a0001c0001t0016g0186 a0002c0002t0006g0187 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+7649C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592279 | |||||||
| chr2:222592356 | C | T | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0002g0231 |
3 | HG01169.hp1 HG01943.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1618+7572G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592356 | |||||||
| chr2:222592357 | G | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+7571C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592357 | |||||||
| chr2:222592415 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+7513G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592415 | |||||||
| chr2:222592474 | C | T | 74 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(71): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1618+7454G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592474 | |||||||
| chr2:222592505 | T | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+7423A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592505 | |||||||
| chr2:222592573 | G | A | 1 | a0002c0002t0004g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1618+7355C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592573 | |||||||
| chr2:222592618 | A | G | 4 | a0001c0001t0008g0282 a0001c0001t0008g0285 a0001c0001t0014g0286 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1618+7310T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592618 | |||||||
| chr2:222592664 | G | A | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+7264C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592664 | |||||||
| chr2:222592682 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1618+7246A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592682 | |||||||
| chr2:222592865 | T | G | 4 | a0001c0001t0005g0310 a0001c0001t0010g0022 a0001c0001t0010g0302 others(1): Show |
5 | HG00639.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1618+7063A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222592865 | |||||||
| chr2:222593044 | G | A | 6 | a0001c0001t0005g0311 a0001c0001t0005g0312 a0001c0001t0005g0313 others(3): Show |
6 | HG01361.hp1 HG01975.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618+6884C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593044 | |||||||
| chr2:222593154 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1618+6774C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593154 | |||||||
| chr2:222593197 | C | T | 1 | a0001c0001t0030g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1618+6731G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593197 | |||||||
| chr2:222593227 | A | G | 1 | a0001c0001t0003g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1618+6701T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593227 | |||||||
| chr2:222593309 | T | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+6619A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593309 | |||||||
| chr2:222593470 | T | C | 11 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(8): Show |
11 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1618+6458A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593470 | |||||||
| chr2:222593493 | G | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0169 a0001c0001t0002g0277 |
4 | NA18956.hp1 NA18966.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+6435C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593493 | |||||||
| chr2:222593495 | G | A | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+6433C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593495 | |||||||
| chr2:222593511 | G | A | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+6417C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593511 | |||||||
| chr2:222593537 | G | T | 279 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1618+6391C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593537 | |||||||
| chr2:222593721 | A | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+6207T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593721 | |||||||
| chr2:222593806 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1618+6122C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593806 | |||||||
| chr2:222593846 | T | G | 21 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(18): Show |
22 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1618+6082A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593846 | |||||||
| chr2:222593853 | C | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+6075G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593853 | |||||||
| chr2:222593988 | G | A | 1 | a0002c0002t0024g0181 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1618+5940C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222593988 | |||||||
| chr2:222594014 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+5914G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594014 | |||||||
| chr2:222594088 | C | A | 2 | a0002c0002t0006g0213 a0002c0002t0006g0214 |
2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1618+5840G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594088 | |||||||
| chr2:222594093 | C | CA | 154 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
169 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1618+5834dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594093 | |||||||
| chr2:222594093 | C | CAA | 84 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0097 others(81): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1618+5833_1618+583 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594093 | |||||||
| chr2:222594093 | C | CAAA | 12 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0046 others(9): Show |
12 | HG01175.hp1 HG01891.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1618+5832_1618+583 others(7): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594093 | |||||||
| chr2:222594093 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0228 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1618+5824_1618+583 others(15): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594093 | |||||||
| chr2:222594120 | G | A | 2 | a0001c0001t0003g0074 a0001c0001t0003g0080 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1618+5808C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594120 | |||||||
| chr2:222594157 | C | T | 7 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618+5771G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594157 | |||||||
| chr2:222594367 | G | A | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+5561C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594367 | |||||||
| chr2:222594447 | T | C | 1 | a0001c0001t0002g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1618+5481A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594447 | |||||||
| chr2:222594451 | C | T | 1 | a0002c0002t0004g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1618+5477G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594451 | |||||||
| chr2:222594771 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1618+5157G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594771 | |||||||
| chr2:222594963 | T | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
95 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.1618+4965A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594963 | |||||||
| chr2:222594987 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
8 | HG01496.hp1 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1618+4941G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222594987 | |||||||
| chr2:222595086 | T | C | 2 | a0002c0002t0004g0204 a0002c0002t0004g0281 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1618+4842A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595086 | |||||||
| chr2:222595322 | A | C | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1618+4606T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595322 | |||||||
| chr2:222595461 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+4467G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595461 | |||||||
| chr2:222595579 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+4349G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595579 | |||||||
| chr2:222595677 | GA | G | 5 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(2): Show |
5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+4250delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595677 | |||||||
| chr2:222595704 | G | A | 2 | a0001c0001t0003g0050 a0001c0001t0003g0051 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1618+4224C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595704 | |||||||
| chr2:222595820 | G | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+4108C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595820 | |||||||
| chr2:222595921 | C | CAT | 31 | a0001c0001t0001g0002 a0001c0001t0001g0086 a0001c0001t0001g0097 others(28): Show |
34 | HG00423.hp2 HG00597.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1618+4005_1618+400 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595921 | |||||||
| chr2:222595921 | C | CATAT | 63 | a0001c0001t0001g0149 a0001c0001t0002g0003 a0001c0001t0002g0016 others(60): Show |
70 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1618+4003_1618+400 others(8): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595921 | |||||||
| chr2:222595921 | C | CATATAT | 11 | a0001c0001t0002g0216 a0001c0001t0002g0219 a0001c0001t0002g0232 others(8): Show |
11 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1618+4001_1618+400 others(10): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595921 | |||||||
| chr2:222595921 | C | CATATATA others(3): Show |
1 | a0001c0001t0002g0254 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1618+3997_1618+400 others(14): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222595921 | |||||||
| chr2:222596183 | C | G | 2 | a0001c0001t0010g0302 a0001c0001t0010g0303 |
2 | HG00639.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1618+3745G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596183 | |||||||
| chr2:222596283 | G | A | 1 | a0001c0001t0003g0073 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1618+3645C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596283 | |||||||
| chr2:222596311 | T | A | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1618+3617A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596311 | |||||||
| chr2:222596392 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+3536T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596392 | |||||||
| chr2:222596423 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+3505T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596423 | |||||||
| chr2:222596499 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0104 a0001c0001t0001g0107 others(3): Show |
7 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1618+3429A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596499 | |||||||
| chr2:222596505 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+3423G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596505 | |||||||
| chr2:222596695 | T | C | 1 | a0002c0002t0024g0181 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1618+3233A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596695 | |||||||
| chr2:222596839 | T | C | 1 | a0002c0002t0024g0181 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1618+3089A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596839 | |||||||
| chr2:222596854 | A | G | 1 | a0001c0001t0002g0258 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1618+3074T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596854 | |||||||
| chr2:222596855 | C | T | 2 | a0001c0001t0005g0314 a0001c0001t0005g0315 |
2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1618+3073G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222596855 | |||||||
| chr2:222597006 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+2922C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597006 | |||||||
| chr2:222597124 | G | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+2804C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597124 | |||||||
| chr2:222597165 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1618+2763C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597165 | |||||||
| chr2:222597341 | T | C | 1 | a0001c0001t0030g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1618+2587A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597341 | |||||||
| chr2:222597557 | A | G | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+2371T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597557 | |||||||
| chr2:222597679 | A | G | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1618+2249T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597679 | |||||||
| chr2:222597754 | C | T | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1618+2174G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597754 | |||||||
| chr2:222597794 | T | A | 1 | a0001c0001t0002g0247 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1618+2134A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222597794 | |||||||
| chr2:222598163 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0123 |
2 | NA18963.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1618+1765G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598163 | |||||||
| chr2:222598255 | T | C | 1 | a0001c0001t0003g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1618+1673A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598255 | |||||||
| chr2:222598420 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1618+1508A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598420 | |||||||
| chr2:222598504 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1618+1424G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598504 | |||||||
| chr2:222598674 | T | C | 5 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(2): Show |
5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+1254A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598674 | |||||||
| chr2:222598753 | G | A | 1 | a0002c0002t0004g0211 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1618+1175C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598753 | |||||||
| chr2:222598812 | G | A | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1618+1116C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598812 | |||||||
| chr2:222598918 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1618+1010C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598918 | |||||||
| chr2:222598941 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1618+987A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598941 | |||||||
| chr2:222598941 | TAA | T | 75 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(72): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1618+985_1618+986d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222598941 | |||||||
| chr2:222599072 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1618+856C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599072 | |||||||
| chr2:222599088 | G | GA | 77 | a0001c0001t0002g0003 a0001c0001t0002g0017 a0001c0001t0002g0018 others(74): Show |
83 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1618+839dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599088 | |||||||
| chr2:222599096 | C | A | 312 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(309): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.1618+832G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599096 | |||||||
| chr2:222599136 | C | T | 6 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0003g0058 others(3): Show |
6 | HG01070.hp2 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1618+792G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599136 | |||||||
| chr2:222599198 | G | A | 4 | a0001c0001t0005g0310 a0001c0001t0010g0022 a0001c0001t0010g0302 others(1): Show |
5 | HG00639.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1618+730C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599198 | |||||||
| chr2:222599322 | G | C | 1 | a0001c0001t0003g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1618+606C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599322 | |||||||
| chr2:222599369 | T | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+559A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599369 | |||||||
| chr2:222599522 | C | A | 1 | a0002c0002t0006g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1618+406G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599522 | |||||||
| chr2:222599732 | C | T | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1618+196G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599732 | |||||||
| chr2:222599795 | T | C | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1618+133A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 16/16 | chr2 | 222599795 | |||||||
| chr2:222600112 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-29C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600112 | |||||||
| chr2:222600226 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-143G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600226 | |||||||
| chr2:222600262 | A | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1463-179T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600262 | |||||||
| chr2:222600291 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1463-208T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600291 | |||||||
| chr2:222600673 | A | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-590T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600673 | |||||||
| chr2:222600679 | C | T | 1 | a0001c0001t0002g0215 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1463-596G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600679 | |||||||
| chr2:222600712 | T | C | 4 | a0001c0001t0003g0024 a0001c0001t0003g0047 a0001c0001t0003g0077 others(1): Show |
4 | HG00323.hp1 HG00639.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-629A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600712 | |||||||
| chr2:222600942 | G | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-859C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222600942 | |||||||
| chr2:222601000 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-917A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601000 | |||||||
| chr2:222601061 | C | CT | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1463-979dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601061 | |||||||
| chr2:222601186 | A | C | 1 | a0002c0002t0006g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1463-1103T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601186 | |||||||
| chr2:222601225 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1463-1142G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601225 | |||||||
| chr2:222601360 | C | T | 1 | a0001c0001t0007g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1463-1277G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601360 | |||||||
| chr2:222601413 | C | CAAT | 3 | a0001c0001t0001g0149 a0001c0001t0002g0264 a0001c0001t0003g0047 |
3 | HG00673.hp1 HG01516.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1463-1333_1463-133 others(7): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601413 | |||||||
| chr2:222601437 | A | T | 1 | a0001c0001t0002g0168 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1463-1354T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601437 | |||||||
| chr2:222601489 | C | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
91 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1463-1406G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601489 | |||||||
| chr2:222601675 | T | C | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1463-1592A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222601675 | |||||||
| chr2:222602009 | A | C | 1 | a0001c0001t0002g0270 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1463-1926T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602009 | |||||||
| chr2:222602042 | C | T | 1 | a0002c0002t0024g0181 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1463-1959G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602042 | |||||||
| chr2:222602140 | C | T | 6 | a0001c0001t0005g0311 a0001c0001t0005g0312 a0001c0001t0005g0313 others(3): Show |
6 | HG01361.hp1 HG01975.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1463-2057G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602140 | |||||||
| chr2:222602192 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1463-2109C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602192 | |||||||
| chr2:222602256 | C | T | 1 | a0001c0001t0008g0291 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1463-2173G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602256 | |||||||
| chr2:222602329 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1463-2246T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602329 | |||||||
| chr2:222602574 | C | A | 2 | a0001c0001t0011g0298 a0001c0001t0011g0299 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1463-2491G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602574 | |||||||
| chr2:222602574 | C | T | 2 | a0001c0001t0011g0300 a0001c0001t0011g0301 |
2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1463-2491G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602574 | |||||||
| chr2:222602574 | CT | C | 15 | a0001c0001t0002g0248 a0002c0002t0006g0011 a0002c0002t0006g0171 others(12): Show |
17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1463-2492delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602574 | |||||||
| chr2:222602614 | T | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-2531A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602614 | |||||||
| chr2:222602632 | T | G | 4 | a0001c0001t0003g0006 a0001c0001t0003g0044 a0001c0001t0003g0045 others(1): Show |
5 | NA18945.hp2 NA18964.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463-2549A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602632 | |||||||
| chr2:222602670 | C | T | 1 | a0001c0001t0031g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1463-2587G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602670 | |||||||
| chr2:222602823 | C | T | 279 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1463-2740G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602823 | |||||||
| chr2:222602862 | C | A | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1463-2779G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602862 | |||||||
| chr2:222602864 | T | C | 1 | a0001c0001t0002g0277 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1463-2781A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602864 | |||||||
| chr2:222602892 | T | A | 6 | a0002c0002t0004g0014 a0002c0002t0004g0015 a0002c0002t0004g0200 others(3): Show |
8 | HG02622.hp1 HG02717.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1463-2809A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222602892 | |||||||
| chr2:222603261 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1463-3178A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603261 | |||||||
| chr2:222603367 | T | C | 1 | a0001c0001t0005g0314 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1463-3284A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603367 | |||||||
| chr2:222603665 | A | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-3582T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603665 | |||||||
| chr2:222603679 | ATATTATA others(3): Show |
A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1463-3606_1463-359 others(14): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603679 | |||||||
| chr2:222603680 | T | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-3597A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603680 | |||||||
| chr2:222603692 | TTA | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-3611_1463-361 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603692 | |||||||
| chr2:222603704 | G | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-3621C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603704 | |||||||
| chr2:222603719 | T | C | 2 | a0001c0001t0002g0248 a0003c0006t0035g0297 |
2 | HG01928.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1463-3636A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603719 | |||||||
| chr2:222603801 | A | G | 5 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(2): Show |
5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463-3718T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603801 | |||||||
| chr2:222603833 | T | C | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1463-3750A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603833 | |||||||
| chr2:222603906 | T | C | 1 | a0001c0001t0005g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1463-3823A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603906 | |||||||
| chr2:222603998 | C | A | 1 | a0002c0002t0004g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1463-3915G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222603998 | |||||||
| chr2:222604210 | T | A | 2 | a0001c0001t0003g0067 a0001c0001t0003g0073 |
2 | NA18979.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1463-4127A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604210 | |||||||
| chr2:222604217 | T | TA | 8 | a0001c0001t0001g0036 a0001c0001t0002g0225 a0001c0001t0003g0058 others(5): Show |
8 | HG00642.hp1 HG01109.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1463-4135dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604217 | |||||||
| chr2:222604348 | C | CAGTG | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-4269_1463-426 others(8): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604348 | |||||||
| chr2:222604495 | T | C | 1 | a0001c0001t0002g0239 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1463-4412A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604495 | |||||||
| chr2:222604672 | C | A | 1 | a0001c0001t0020g0021 | 2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1463-4589G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604672 | |||||||
| chr2:222604722 | A | AT | 166 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(163): Show |
181 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.1463-4640dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604722 | |||||||
| chr2:222604722 | A | ATT | 32 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(29): Show |
33 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1463-4641_1463-464 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604722 | |||||||
| chr2:222604722 | A | ATTT | 49 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(46): Show |
54 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1463-4642_1463-464 others(7): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604722 | |||||||
| chr2:222604722 | ATTTTTT | A | 17 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(14): Show |
18 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1463-4645_1463-464 others(10): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604722 | |||||||
| chr2:222604836 | G | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-4753C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604836 | |||||||
| chr2:222604975 | T | TG | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1463-4893dupC | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222604975 | |||||||
| chr2:222605125 | A | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1463-5042T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605125 | |||||||
| chr2:222605158 | A | ACTCTCTC others(7): Show |
1 | a0001c0001t0003g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1463-5076_1463-507 others(18): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605158 | |||||||
| chr2:222605161 | T | C | 1 | a0001c0001t0003g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1463-5078A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TACTTTCT others(13): Show |
1 | a0001c0001t0005g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1463-5079_1463-507 others(24): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TCTCTCTC others(8): Show |
6 | a0001c0001t0001g0036 a0001c0001t0001g0120 a0001c0001t0001g0141 others(3): Show |
6 | HG00673.hp1 HG02027.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1463-5079_1463-507 others(19): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TCTCTCTC others(10): Show |
2 | a0001c0001t0011g0301 a0002c0002t0006g0187 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1463-5079_1463-507 others(21): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TCTCTCTC others(12): Show |
1 | a0001c0001t0001g0122 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1463-5079_1463-507 others(23): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TCTCTCTC others(14): Show |
2 | a0001c0001t0001g0105 a0001c0001t0005g0318 |
2 | HG01361.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1463-5079_1463-507 others(25): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTC | 5 | a0001c0001t0002g0268 a0001c0001t0002g0274 a0001c0001t0007g0154 others(2): Show |
5 | HG00642.hp2 HG01891.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1463-5080_1463-507 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTC | 48 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(45): Show |
53 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1463-5082_1463-507 others(8): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTC | 8 | a0001c0001t0003g0045 a0001c0001t0003g0074 a0001c0001t0003g0080 others(5): Show |
8 | HG01069.hp2 HG01071.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1463-5084_1463-507 others(10): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(1): Show |
10 | a0001c0001t0001g0126 a0001c0001t0001g0184 a0001c0001t0001g0293 others(7): Show |
11 | HG01261.hp2 HG01928.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1463-5086_1463-507 others(12): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(3): Show |
53 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0108 others(50): Show |
59 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1463-5088_1463-507 others(14): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(5): Show |
16 | a0001c0001t0001g0008 a0001c0001t0001g0088 a0001c0001t0001g0097 others(13): Show |
17 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1463-5090_1463-507 others(16): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(7): Show |
45 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(42): Show |
50 | HG00741.hp2 HG01070.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.1463-5092_1463-507 others(18): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(9): Show |
12 | a0001c0001t0001g0085 a0001c0001t0001g0091 a0001c0001t0001g0104 others(9): Show |
12 | HG00280.hp2 HG01192.hp1 HG03225.hp2 others(9): Show |
intron_variant | MODIFIER | c.1463-5094_1463-507 others(20): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(11): Show |
14 | a0001c0001t0001g0099 a0001c0001t0001g0121 a0001c0001t0001g0143 others(11): Show |
15 | HG00735.hp1 HG01106.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.1463-5096_1463-507 others(22): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(13): Show |
6 | a0001c0001t0005g0307 a0001c0001t0005g0316 a0001c0001t0010g0022 others(3): Show |
7 | HG02109.hp2 HG02257.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1463-5098_1463-507 others(24): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(15): Show |
6 | a0001c0001t0001g0123 a0001c0001t0005g0310 a0001c0001t0005g0317 others(3): Show |
6 | HG00639.hp2 HG00735.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1463-5100_1463-507 others(26): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(17): Show |
3 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0309 |
3 | HG01884.hp2 HG02572.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1463-5102_1463-507 others(28): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(25): Show |
1 | a0001c0001t0005g0313 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1463-5110_1463-507 others(36): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605161 | T | TTCTCTCT others(29): Show |
1 | a0001c0001t0005g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1463-5079_1463-507 others(40): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605161 | |||||||
| chr2:222605195 | G | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0107 a0001c0001t0001g0130 others(2): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1463-5112C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605195 | |||||||
| chr2:222605264 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-5181G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605264 | |||||||
| chr2:222605384 | T | A | 1 | a0002c0002t0006g0214 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1463-5301A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605384 | |||||||
| chr2:222605547 | T | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-5464A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605547 | |||||||
| chr2:222605683 | C | T | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1463-5600G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605683 | |||||||
| chr2:222605754 | C | CA | 279 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1463-5672dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605754 | |||||||
| chr2:222605808 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-5725T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605808 | |||||||
| chr2:222605928 | A | C | 1 | a0001c0001t0001g0125 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1463-5845T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222605928 | |||||||
| chr2:222606069 | A | ATTTCTAG others(3): Show |
1 | a0001c0001t0003g0026 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1463-5996_1463-598 others(14): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606069 | |||||||
| chr2:222606128 | G | A | 1 | a0001c0001t0019g0249 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1463-6045C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606128 | |||||||
| chr2:222606193 | G | A | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1463-6110C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606193 | |||||||
| chr2:222606287 | C | T | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1463-6204G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606287 | |||||||
| chr2:222606361 | AG | A | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1463-6279delC | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606361 | |||||||
| chr2:222606549 | C | G | 78 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0017 others(75): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1463-6466G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606549 | |||||||
| chr2:222606651 | T | G | 1 | a0001c0001t0016g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1463-6568A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606651 | |||||||
| chr2:222606685 | C | A | 1 | a0001c0001t0002g0250 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1463-6602G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606685 | |||||||
| chr2:222606717 | T | A | 1 | a0001c0007t0002g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1463-6634A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606717 | |||||||
| chr2:222606735 | G | A | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1463-6652C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606735 | |||||||
| chr2:222606740 | G | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463-6657C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606740 | |||||||
| chr2:222606896 | G | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1463-6813C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222606896 | |||||||
| chr2:222607225 | T | C | 2 | a0001c0001t0005g0311 a0001c0001t0005g0313 |
2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1462+6586A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607225 | |||||||
| chr2:222607259 | T | G | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0132 others(2): Show |
5 | HG00735.hp2 HG01257.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1462+6552A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607259 | |||||||
| chr2:222607591 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1462+6220C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607591 | |||||||
| chr2:222607605 | C | T | 15 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1462+6206G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607605 | |||||||
| chr2:222607649 | A | T | 275 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(272): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1462+6162T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607649 | |||||||
| chr2:222607650 | A | T | 1 | a0001c0001t0003g0026 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1462+6161T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607650 | |||||||
| chr2:222607742 | T | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+6069A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607742 | |||||||
| chr2:222607747 | T | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+6064A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607747 | |||||||
| chr2:222607748 | A | T | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1462+6063T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607748 | |||||||
| chr2:222607753 | G | A | 73 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(70): Show |
79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1462+6058C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607753 | |||||||
| chr2:222607974 | C | A | 1 | a0001c0001t0002g0168 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1462+5837G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222607974 | |||||||
| chr2:222608264 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1462+5547T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608264 | |||||||
| chr2:222608280 | A | G | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462+5531T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608280 | |||||||
| chr2:222608482 | T | C | 5 | a0001c0001t0005g0310 a0001c0001t0010g0022 a0001c0001t0010g0302 others(2): Show |
6 | HG00639.hp2 HG01928.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1462+5329A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608482 | |||||||
| chr2:222608498 | C | T | 14 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(11): Show |
14 | HG01361.hp1 HG01884.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1462+5313G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608498 | |||||||
| chr2:222608589 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1462+5222T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608589 | |||||||
| chr2:222608614 | A | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0026 a0001c0001t0003g0031 |
4 | HG01952.hp2 NA19010.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1462+5197T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608614 | |||||||
| chr2:222608675 | G | C | 2 | a0001c0001t0002g0254 a0001c0001t0002g0256 |
2 | HG01255.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1462+5136C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608675 | |||||||
| chr2:222608794 | T | G | 3 | a0001c0001t0003g0039 a0001c0001t0021g0040 a0001c0001t0022g0041 |
3 | HG00140.hp2 HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1462+5017A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222608794 | |||||||
| chr2:222609622 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462+4189G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609622 | |||||||
| chr2:222609671 | G | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+4140C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609671 | |||||||
| chr2:222609715 | T | C | 1 | a0001c0001t0003g0028 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1462+4096A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609715 | |||||||
| chr2:222609767 | T | A | 4 | a0001c0001t0003g0024 a0001c0001t0003g0047 a0001c0001t0003g0077 others(1): Show |
4 | HG00323.hp1 HG00639.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462+4044A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609767 | |||||||
| chr2:222609768 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1462+4043A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609768 | |||||||
| chr2:222609911 | A | G | 11 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(8): Show |
11 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1462+3900T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609911 | |||||||
| chr2:222609913 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1462+3898C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609913 | |||||||
| chr2:222609978 | G | A | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1462+3833C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222609978 | |||||||
| chr2:222610028 | A | T | 74 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(71): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1462+3783T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610028 | |||||||
| chr2:222610048 | A | G | 1 | a0001c0001t0008g0289 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1462+3763T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610048 | |||||||
| chr2:222610060 | A | G | 1 | a0001c0001t0008g0289 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1462+3751T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610060 | |||||||
| chr2:222610475 | A | G | 75 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(72): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1462+3336T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610475 | |||||||
| chr2:222610493 | AT | A | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1462+3317delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610493 | |||||||
| chr2:222610503 | G | A | 75 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(72): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1462+3308C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610503 | |||||||
| chr2:222610525 | A | T | 6 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0010g0022 others(3): Show |
7 | HG00639.hp2 HG01928.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1462+3286T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610525 | |||||||
| chr2:222610602 | T | A | 1 | a0001c0001t0002g0251 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1462+3209A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610602 | |||||||
| chr2:222610691 | T | C | 1 | a0002c0002t0006g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1462+3120A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610691 | |||||||
| chr2:222610804 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0035 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1462+3007A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610804 | |||||||
| chr2:222610926 | C | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+2885G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222610926 | |||||||
| chr2:222611053 | A | G | 2 | a0002c0002t0006g0011 a0002c0002t0006g0178 |
3 | HG02109.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1462+2758T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611053 | |||||||
| chr2:222611448 | C | CG | 21 | a0001c0001t0001g0033 a0001c0001t0002g0239 a0001c0001t0005g0304 others(18): Show |
22 | HG00639.hp2 HG00735.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1462+2362dupC | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611448 | |||||||
| chr2:222611457 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1462+2354C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611457 | |||||||
| chr2:222611459 | G | A | 7 | a0001c0001t0007g0038 a0001c0001t0007g0087 a0001c0001t0007g0134 others(4): Show |
7 | HG00280.hp2 HG00735.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1462+2352C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611459 | |||||||
| chr2:222611552 | G | A | 277 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(274): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1462+2259C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611552 | |||||||
| chr2:222611590 | G | A | 1 | a0001c0001t0005g0312 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1462+2221C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611590 | |||||||
| chr2:222611661 | C | G | 14 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(11): Show |
16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1462+2150G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611661 | |||||||
| chr2:222611815 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+1996G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611815 | |||||||
| chr2:222611971 | G | A | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1462+1840C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611971 | |||||||
| chr2:222611981 | C | T | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1462+1830G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222611981 | |||||||
| chr2:222612235 | T | C | 7 | a0002c0002t0004g0173 a0002c0002t0004g0193 a0002c0002t0004g0204 others(4): Show |
7 | HG01257.hp1 HG02145.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1462+1576A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612235 | |||||||
| chr2:222612259 | T | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462+1552A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612259 | |||||||
| chr2:222612441 | A | G | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1462+1370T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612441 | |||||||
| chr2:222612448 | G | A | 1 | a0001c0001t0007g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1462+1363C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612448 | |||||||
| chr2:222612459 | G | T | 2 | a0001c0001t0002g0275 a0001c0001t0002g0276 |
2 | NA19009.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1462+1352C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612459 | |||||||
| chr2:222612466 | C | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1462+1345G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612466 | |||||||
| chr2:222612512 | C | A | 3 | a0001c0001t0010g0022 a0001c0001t0010g0302 a0001c0001t0010g0303 |
4 | HG00639.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1462+1299G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612512 | |||||||
| chr2:222612561 | G | A | 1 | a0001c0004t0002g0100 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1462+1250C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612561 | |||||||
| chr2:222612718 | T | C | 19 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(16): Show |
20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1462+1093A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612718 | |||||||
| chr2:222612729 | C | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462+1082G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612729 | |||||||
| chr2:222612730 | C | CAATGCAC others(11): Show |
1 | a0001c0001t0002g0292 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1462+1063_1462+108 others(22): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612730 | |||||||
| chr2:222612743 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1462+1068C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612743 | |||||||
| chr2:222612910 | A | G | 3 | a0001c0001t0012g0037 a0001c0001t0012g0062 a0001c0001t0012g0063 |
3 | HG02615.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1462+901T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222612910 | |||||||
| chr2:222613013 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1462+798T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613013 | |||||||
| chr2:222613044 | G | A | 2 | a0001c0001t0002g0226 a0001c0001t0002g0227 |
2 | NA18984.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1462+767C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613044 | |||||||
| chr2:222613049 | A | G | 1 | a0001c0001t0003g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1462+762T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613049 | |||||||
| chr2:222613239 | G | T | 2 | a0001c0001t0002g0238 a0001c0001t0002g0260 |
2 | NA19010.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1462+572C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613239 | |||||||
| chr2:222613374 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1462+437C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613374 | |||||||
| chr2:222613435 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1462+376G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613435 | |||||||
| chr2:222613727 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1462+84A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613727 | |||||||
| chr2:222613780 | A | C | 1 | a0002c0002t0004g0202 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1462+31T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 15/16 | chr2 | 222613780 | |||||||
| chr2:222614146 | A | C | 3 | a0001c0001t0003g0039 a0001c0001t0021g0040 a0001c0001t0022g0041 |
3 | HG00140.hp2 HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1345-218T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222614146 | |||||||
| chr2:222614286 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1345-358T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222614286 | |||||||
| chr2:222614494 | C | A | 1 | a0001c0001t0005g0312 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1345-566G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222614494 | |||||||
| chr2:222614561 | T | C | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1345-633A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222614561 | |||||||
| chr2:222615210 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1345-1282C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615210 | |||||||
| chr2:222615237 | T | C | 3 | a0001c0001t0003g0053 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02615.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1345-1309A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615237 | |||||||
| chr2:222615276 | T | A | 4 | a0002c0002t0009g0012 a0002c0002t0009g0172 a0002c0002t0009g0177 others(1): Show |
5 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345-1348A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615276 | |||||||
| chr2:222615412 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-1484G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615412 | |||||||
| chr2:222615984 | A | C | 2 | a0002c0002t0004g0161 a0004c0003t0004g0160 |
2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1345-2056T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615984 | |||||||
| chr2:222615996 | T | A | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1345-2068A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222615996 | |||||||
| chr2:222616254 | A | G | 11 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(8): Show |
11 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1345-2326T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616254 | |||||||
| chr2:222616398 | T | G | 1 | a0001c0001t0002g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1345-2470A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616398 | |||||||
| chr2:222616407 | C | T | 7 | a0002c0002t0004g0173 a0002c0002t0004g0193 a0002c0002t0004g0204 others(4): Show |
7 | HG01257.hp1 HG02145.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345-2479G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616407 | |||||||
| chr2:222616454 | G | C | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1345-2526C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616454 | |||||||
| chr2:222616455 | G | A | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1345-2527C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616455 | |||||||
| chr2:222616528 | A | G | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1345-2600T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616528 | |||||||
| chr2:222616545 | C | CA | 60 | a0001c0001t0002g0227 a0001c0001t0003g0001 a0001c0001t0003g0004 others(57): Show |
66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1345-2618dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616545 | |||||||
| chr2:222616545 | C | CAA | 76 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(73): Show |
83 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1345-2619_1345-261 others(6): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616545 | |||||||
| chr2:222616545 | C | CAAA | 86 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
92 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.1345-2620_1345-261 others(7): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616545 | |||||||
| chr2:222616545 | C | CAAAA | 6 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0001t0001g0125 others(3): Show |
6 | HG02027.hp2 HG04199.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-2621_1345-261 others(8): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616545 | |||||||
| chr2:222616571 | C | G | 2 | a0002c0002t0006g0213 a0002c0002t0006g0214 |
2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1345-2643G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616571 | |||||||
| chr2:222616893 | G | A | 4 | a0001c0001t0008g0282 a0001c0001t0008g0285 a0001c0001t0014g0286 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+2752C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616893 | |||||||
| chr2:222616906 | G | A | 39 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(36): Show |
43 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.1344+2739C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616906 | |||||||
| chr2:222616971 | CAGAAAGA others(282): Show |
C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1344+2385_1344+267 others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616971 | |||||||
| chr2:222616985 | C | CT | 18 | a0001c0001t0002g0003 a0001c0001t0002g0020 a0001c0001t0002g0169 others(15): Show |
18 | HG00438.hp1 HG00597.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.1344+2659dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222616985 | |||||||
| chr2:222617460 | A | G | 94 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(91): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.1344+2185T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617460 | |||||||
| chr2:222617476 | A | G | 19 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(16): Show |
20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1344+2169T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617476 | |||||||
| chr2:222617585 | A | G | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1344+2060T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617585 | |||||||
| chr2:222617613 | G | A | 1 | a0002c0002t0004g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1344+2032C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617613 | |||||||
| chr2:222617630 | T | C | 1 | a0001c0001t0002g0018 | 2 | NA18952.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1344+2015A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617630 | |||||||
| chr2:222617657 | G | A | 1 | a0001c0001t0033g0137 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1344+1988C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617657 | |||||||
| chr2:222617694 | T | G | 25 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(22): Show |
26 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1344+1951A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617694 | |||||||
| chr2:222617775 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0130 |
2 | HG00741.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1344+1870G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617775 | |||||||
| chr2:222617776 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1344+1869C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617776 | |||||||
| chr2:222617819 | G | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
91 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1344+1826C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617819 | |||||||
| chr2:222617861 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0106 |
2 | NA18962.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1344+1784G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617861 | |||||||
| chr2:222617957 | G | A | 1 | a0002c0002t0004g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1344+1688C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617957 | |||||||
| chr2:222617972 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1344+1673C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222617972 | |||||||
| chr2:222618098 | T | C | 19 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(16): Show |
20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1344+1547A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618098 | |||||||
| chr2:222618175 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1344+1470T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618175 | |||||||
| chr2:222618226 | T | A | 14 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(11): Show |
16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1344+1419A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618226 | |||||||
| chr2:222618444 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1344+1201T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618444 | |||||||
| chr2:222618516 | T | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+1129A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618516 | |||||||
| chr2:222618587 | T | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+1058A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618587 | |||||||
| chr2:222618592 | T | C | 1 | a0001c0001t0002g0292 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1344+1053A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618592 | |||||||
| chr2:222618857 | A | G | 1 | a0001c0001t0005g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1344+788T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618857 | |||||||
| chr2:222618876 | C | A | 1 | a0002c0002t0004g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1344+769G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618876 | |||||||
| chr2:222618951 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1344+694C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618951 | |||||||
| chr2:222618969 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+676G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222618969 | |||||||
| chr2:222619156 | T | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1344+489A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619156 | |||||||
| chr2:222619319 | TA | T | 110 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0106 others(107): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1344+325delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619319 | |||||||
| chr2:222619319 | TAA | T | 42 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(39): Show |
46 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.1344+324_1344+325d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619319 | |||||||
| chr2:222619320 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1344+325T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619320 | |||||||
| chr2:222619387 | G | A | 39 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(36): Show |
43 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.1344+258C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619387 | |||||||
| chr2:222619508 | A | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(36): Show |
43 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.1344+137T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619508 | |||||||
| chr2:222619606 | A | C | 5 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(2): Show |
5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+39T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 14/16 | chr2 | 222619606 | |||||||
| chr2:222619881 | G | T | 1 | a0001c0001t0002g0254 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1252-144C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222619881 | |||||||
| chr2:222619909 | A | T | 2 | a0001c0001t0002g0226 a0001c0001t0002g0227 |
2 | NA18984.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1252-172T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222619909 | |||||||
| chr2:222620072 | T | G | 3 | a0001c0001t0007g0087 a0001c0001t0007g0138 a0001c0001t0007g0139 |
3 | HG00735.hp1 HG01256.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1252-335A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620072 | |||||||
| chr2:222620291 | T | C | 1 | a0001c0001t0011g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1252-554A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620291 | |||||||
| chr2:222620385 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1252-648A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620385 | |||||||
| chr2:222620439 | T | C | 4 | a0002c0002t0009g0012 a0002c0002t0009g0172 a0002c0002t0009g0177 others(1): Show |
5 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1252-702A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620439 | |||||||
| chr2:222620460 | A | G | 1 | a0001c0001t0008g0288 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1252-723T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620460 | |||||||
| chr2:222620590 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0126 |
2 | HG02027.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1252-853C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620590 | |||||||
| chr2:222620653 | T | C | 87 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(84): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1252-916A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620653 | |||||||
| chr2:222620711 | G | A | 37 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(34): Show |
41 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.1252-974C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222620711 | |||||||
| chr2:222621038 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1252-1301T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621038 | |||||||
| chr2:222621069 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1252-1332A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621069 | |||||||
| chr2:222621328 | G | A | 13 | a0001c0001t0001g0127 a0002c0002t0006g0171 a0002c0002t0006g0174 others(10): Show |
14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1252-1591C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621328 | |||||||
| chr2:222621386 | C | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1252-1649G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621386 | |||||||
| chr2:222621470 | G | T | 3 | a0002c0002t0009g0012 a0002c0002t0009g0177 a0002c0002t0009g0179 |
4 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1252-1733C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621470 | |||||||
| chr2:222621778 | T | C | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1251+1872A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621778 | |||||||
| chr2:222621949 | T | C | 1 | a0001c0001t0002g0232 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1251+1701A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222621949 | |||||||
| chr2:222622068 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1251+1582G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622068 | |||||||
| chr2:222622113 | G | C | 2 | a0001c0001t0003g0077 a0001c0001t0003g0078 |
2 | HG00639.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1251+1537C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622113 | |||||||
| chr2:222622208 | A | G | 1 | a0001c0001t0005g0310 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1251+1442T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622208 | |||||||
| chr2:222622235 | C | T | 1 | a0001c0001t0002g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1251+1415G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622235 | |||||||
| chr2:222622439 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1251+1211T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622439 | |||||||
| chr2:222622503 | G | A | 74 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(71): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.1251+1147C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622503 | |||||||
| chr2:222622635 | C | T | 1 | a0001c0004t0002g0100 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1251+1015G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622635 | |||||||
| chr2:222622772 | G | A | 2 | a0002c0002t0004g0204 a0002c0002t0004g0281 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1251+878C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622772 | |||||||
| chr2:222622841 | T | C | 1 | a0001c0001t0002g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1251+809A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622841 | |||||||
| chr2:222622924 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1251+726C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222622924 | |||||||
| chr2:222623063 | GAA | G | 14 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(11): Show |
16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1251+585_1251+586d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222623063 | |||||||
| chr2:222623067 | T | G | 14 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(11): Show |
16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1251+583A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222623067 | |||||||
| chr2:222623088 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1251+562C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222623088 | |||||||
| chr2:222623517 | C | G | 3 | a0001c0001t0016g0185 a0001c0001t0016g0186 a0002c0002t0006g0187 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1251+133G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 13/16 | chr2 | 222623517 | |||||||
| chr2:222623734 | A | G | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1171-4T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222623734 | |||||||
| chr2:222623868 | C | T | 3 | a0001c0001t0016g0185 a0001c0001t0016g0186 a0002c0002t0006g0187 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1171-138G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222623868 | |||||||
| chr2:222623989 | C | T | 1 | a0002c0002t0004g0192 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1171-259G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222623989 | |||||||
| chr2:222624059 | T | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(236): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1170+213A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222624059 | |||||||
| chr2:222624207 | C | G | 1 | a0001c0001t0003g0052 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1170+65G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222624207 | |||||||
| chr2:222624260 | G | A | 4 | a0001c0001t0002g0232 a0001c0001t0002g0254 a0001c0001t0002g0256 others(1): Show |
4 | HG01255.hp1 HG01346.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+12C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 12/16 | chr2 | 222624260 | |||||||
| chr2:222624530 | GT | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.963-52delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 11/16 | chr2 | 222624530 | |||||||
| chr2:222624574 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.963-95G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 11/16 | chr2 | 222624574 | |||||||
| chr2:222624703 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.962+11A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 11/16 | chr2 | 222624703 | |||||||
| chr2:222625071 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.901-296C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625071 | |||||||
| chr2:222625094 | C | T | 2 | a0001c0001t0011g0298 a0001c0001t0011g0299 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.901-319G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625094 | |||||||
| chr2:222625134 | G | T | 1 | a0001c0001t0002g0267 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.901-359C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625134 | |||||||
| chr2:222625491 | G | A | 2 | a0002c0002t0006g0175 a0002c0002t0006g0176 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.901-716C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625491 | |||||||
| chr2:222625708 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.901-933G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625708 | |||||||
| chr2:222625845 | T | C | 2 | a0001c0001t0005g0314 a0001c0001t0005g0315 |
2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.901-1070A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625845 | |||||||
| chr2:222625855 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.901-1080G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625855 | |||||||
| chr2:222625890 | T | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.901-1115A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625890 | |||||||
| chr2:222625942 | T | C | 5 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(2): Show |
5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.901-1167A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222625942 | |||||||
| chr2:222626141 | C | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.901-1366G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626141 | |||||||
| chr2:222626243 | C | CA | 86 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
92 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.901-1469dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626243 | |||||||
| chr2:222626243 | C | CAA | 13 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0130 others(10): Show |
13 | HG00140.hp1 HG00280.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.901-1470_901-1469d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626243 | |||||||
| chr2:222626243 | CA | C | 11 | a0001c0001t0002g0168 a0001c0001t0003g0048 a0001c0001t0003g0052 others(8): Show |
12 | HG02109.hp1 HG02280.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.901-1469delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626243 | |||||||
| chr2:222626287 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.901-1512T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626287 | |||||||
| chr2:222626402 | A | G | 18 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(15): Show |
19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.901-1627T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626402 | |||||||
| chr2:222626455 | A | G | 15 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(12): Show |
17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.901-1680T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626455 | |||||||
| chr2:222626549 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.901-1774G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626549 | |||||||
| chr2:222626805 | G | A | 1 | a0002c0002t0004g0192 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.901-2030C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626805 | |||||||
| chr2:222626851 | G | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
95 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.900+1986C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626851 | |||||||
| chr2:222626904 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.900+1933G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626904 | |||||||
| chr2:222626909 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.900+1928C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626909 | |||||||
| chr2:222626929 | G | A | 1 | a0001c0001t0030g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.900+1908C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222626929 | |||||||
| chr2:222627014 | C | T | 32 | a0002c0002t0004g0013 a0002c0002t0004g0014 a0002c0002t0004g0015 others(29): Show |
35 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.900+1823G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627014 | |||||||
| chr2:222627203 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
93 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.900+1634T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627203 | |||||||
| chr2:222627208 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0159 a0001c0001t0034g0163 |
3 | HG00735.hp2 HG01516.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.900+1629A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627208 | |||||||
| chr2:222627422 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.900+1415C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627422 | |||||||
| chr2:222627446 | C | T | 18 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(15): Show |
19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.900+1391G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627446 | |||||||
| chr2:222627464 | G | A | 2 | a0002c0002t0006g0213 a0002c0002t0006g0214 |
2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.900+1373C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627464 | |||||||
| chr2:222627568 | T | G | 5 | a0002c0002t0004g0173 a0002c0002t0004g0193 a0002c0002t0004g0204 others(2): Show |
5 | HG02976.hp1 HG03139.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+1269A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627568 | |||||||
| chr2:222627933 | C | T | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.900+904G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627933 | |||||||
| chr2:222627988 | T | C | 1 | a0002c0002t0004g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.900+849A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222627988 | |||||||
| chr2:222628044 | C | T | 2 | a0001c0001t0011g0298 a0001c0001t0011g0299 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.900+793G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628044 | |||||||
| chr2:222628083 | T | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
92 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.900+754A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628083 | |||||||
| chr2:222628145 | C | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.900+692G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628145 | |||||||
| chr2:222628260 | C | T | 18 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(15): Show |
19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.900+577G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628260 | |||||||
| chr2:222628302 | C | T | 32 | a0002c0002t0004g0013 a0002c0002t0004g0014 a0002c0002t0004g0015 others(29): Show |
35 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.900+535G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628302 | |||||||
| chr2:222628355 | A | G | 1 | a0001c0001t0011g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.900+482T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628355 | |||||||
| chr2:222628498 | A | C | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.900+339T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628498 | |||||||
| chr2:222628533 | T | C | 2 | a0002c0002t0004g0189 a0002c0002t0004g0190 |
2 | NA18955.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.900+304A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628533 | |||||||
| chr2:222628706 | T | C | 19 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(16): Show |
20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.900+131A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628706 | |||||||
| chr2:222628716 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(234): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.900+121C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628716 | |||||||
| chr2:222628721 | G | A | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.900+116C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628721 | |||||||
| chr2:222628724 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.900+113A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628724 | |||||||
| chr2:222628738 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.900+99C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 10/16 | chr2 | 222628738 | |||||||
| chr2:222629079 | C | G | 12 | a0002c0002t0006g0011 a0002c0002t0006g0174 a0002c0002t0006g0175 others(9): Show |
14 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.849-191G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222629079 | |||||||
| chr2:222629485 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.849-597A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222629485 | |||||||
| chr2:222629490 | G | A | 1 | a0002c0002t0006g0174 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849-602C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222629490 | |||||||
| chr2:222629818 | G | A | 2 | a0001c0001t0003g0074 a0001c0001t0003g0080 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.848+295C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222629818 | |||||||
| chr2:222629980 | A | G | 1 | a0001c0001t0005g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.848+133T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222629980 | |||||||
| chr2:222630066 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.848+47G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 9/16 | chr2 | 222630066 | |||||||
| chr2:222630414 | A | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.787-240T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630414 | |||||||
| chr2:222630500 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.787-326C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630500 | |||||||
| chr2:222630543 | T | C | 1 | a0001c0001t0007g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.787-369A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630543 | |||||||
| chr2:222630758 | A | G | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.787-584T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630758 | |||||||
| chr2:222630813 | A | T | 15 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(12): Show |
17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.787-639T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630813 | |||||||
| chr2:222630957 | T | A | 1 | a0002c0002t0004g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.786+647A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222630957 | |||||||
| chr2:222631182 | CT | C | 26 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(23): Show |
28 | HG00639.hp2 HG01361.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.786+421delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631182 | |||||||
| chr2:222631250 | A | C | 2 | a0001c0001t0002g0235 a0001c0001t0002g0264 |
2 | NA18959.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.786+354T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631250 | |||||||
| chr2:222631265 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.786+339A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631265 | |||||||
| chr2:222631277 | G | A | 2 | a0002c0002t0006g0213 a0002c0002t0006g0214 |
2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.786+327C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631277 | |||||||
| chr2:222631325 | A | G | 5 | a0002c0002t0004g0173 a0002c0002t0004g0193 a0002c0002t0004g0204 others(2): Show |
5 | HG02976.hp1 HG03139.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+279T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631325 | |||||||
| chr2:222631357 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(234): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.786+247C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631357 | |||||||
| chr2:222631391 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.786+213T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631391 | |||||||
| chr2:222631490 | A | G | 4 | a0001c0001t0008g0282 a0001c0001t0008g0285 a0001c0001t0014g0286 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+114T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 8/16 | chr2 | 222631490 | |||||||
| chr2:222631847 | C | T | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.716-173G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222631847 | |||||||
| chr2:222631898 | C | T | 30 | a0002c0002t0004g0013 a0002c0002t0004g0014 a0002c0002t0004g0015 others(27): Show |
33 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.716-224G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222631898 | |||||||
| chr2:222631932 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.716-258G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222631932 | |||||||
| chr2:222631980 | G | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.716-306C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222631980 | |||||||
| chr2:222632023 | G | GATGGTGC others(11): Show |
14 | a0001c0001t0001g0093 a0001c0001t0005g0304 a0001c0001t0005g0305 others(11): Show |
14 | HG01257.hp2 HG01361.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.716-367_716-350dup others(18): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632023 | |||||||
| chr2:222632023 | GATGGTGC others(11): Show |
G | 16 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(13): Show |
18 | HG01928.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.716-367_716-350del others(18): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632023 | |||||||
| chr2:222632056 | C | A | 1 | a0001c0001t0002g0231 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.716-382G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632056 | |||||||
| chr2:222632069 | T | C | 32 | a0002c0002t0004g0013 a0002c0002t0004g0014 a0002c0002t0004g0015 others(29): Show |
35 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.716-395A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632069 | |||||||
| chr2:222632076 | A | AGAGTG | 2 | a0001c0001t0001g0009 a0001c0001t0001g0158 |
3 | NA18982.hp2 NA19007.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.716-407_716-403dup others(5): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632076 | |||||||
| chr2:222632142 | AT | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.716-469delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632142 | |||||||
| chr2:222632143 | T | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.716-469A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632143 | |||||||
| chr2:222632151 | A | G | 81 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(78): Show |
90 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.716-477T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632151 | |||||||
| chr2:222632198 | C | G | 1 | a0001c0001t0002g0234 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.716-524G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632198 | |||||||
| chr2:222632241 | C | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.716-567G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632241 | |||||||
| chr2:222632248 | T | C | 1 | a0002c0002t0024g0181 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.716-574A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632248 | |||||||
| chr2:222632293 | G | A | 1 | a0001c0001t0008g0291 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.716-619C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632293 | |||||||
| chr2:222632432 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
90 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.716-758G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632432 | |||||||
| chr2:222632792 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.715+407G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632792 | |||||||
| chr2:222632840 | C | A | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.715+359G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632840 | |||||||
| chr2:222632842 | A | AC | 4 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0001t0003g0050 others(1): Show |
4 | HG01243.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+356_715+357ins others(1): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632842 | |||||||
| chr2:222632843 | A | C | 6 | a0001c0001t0001g0098 a0002c0002t0004g0204 a0002c0002t0004g0281 others(3): Show |
6 | HG01891.hp1 HG01928.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.715+356T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632843 | |||||||
| chr2:222632914 | T | C | 81 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(78): Show |
90 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.715+285A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632914 | |||||||
| chr2:222632997 | G | A | 3 | a0001c0001t0016g0185 a0001c0001t0016g0186 a0002c0002t0006g0187 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.715+202C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222632997 | |||||||
| chr2:222633120 | A | T | 1 | a0002c0002t0006g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.715+79T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222633120 | |||||||
| chr2:222633148 | G | A | 2 | a0001c0001t0011g0300 a0001c0001t0011g0301 |
2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.715+51C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 7/16 | chr2 | 222633148 | |||||||
| chr2:222633337 | GT | G | 5 | a0002c0002t0004g0014 a0002c0002t0004g0200 a0002c0002t0004g0201 others(2): Show |
6 | HG01928.hp1 HG02622.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-31delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633337 | |||||||
| chr2:222633355 | T | C | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.607-48A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633355 | |||||||
| chr2:222633448 | T | C | 96 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(93): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.607-141A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633448 | |||||||
| chr2:222633455 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.607-148C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633455 | |||||||
| chr2:222633500 | T | A | 66 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(63): Show |
73 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.607-193A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633500 | |||||||
| chr2:222633514 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.607-207G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633514 | |||||||
| chr2:222633543 | G | A | 1 | a0001c0001t0005g0310 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.607-236C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633543 | |||||||
| chr2:222633554 | T | C | 1 | a0001c0001t0007g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.607-247A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633554 | |||||||
| chr2:222633579 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.607-272C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633579 | |||||||
| chr2:222633645 | G | A | 18 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(15): Show |
19 | HG00639.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.607-338C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633645 | |||||||
| chr2:222633670 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.607-363C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633670 | |||||||
| chr2:222633682 | CA | C | 36 | a0001c0001t0002g0222 a0001c0001t0003g0075 a0001c0001t0003g0076 others(33): Show |
39 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.607-376delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633682 | |||||||
| chr2:222633682 | CAA | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(182): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.607-377_607-376del others(2): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633682 | |||||||
| chr2:222633908 | G | A | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.606+483C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633908 | |||||||
| chr2:222633944 | T | C | 3 | a0001c0001t0016g0185 a0001c0001t0016g0186 a0002c0002t0006g0187 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.606+447A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633944 | |||||||
| chr2:222633957 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.606+434G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222633957 | |||||||
| chr2:222634119 | A | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.606+272T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222634119 | |||||||
| chr2:222634358 | C | T | 66 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(63): Show |
73 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.606+33G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 6/16 | chr2 | 222634358 | |||||||
| chr2:222634934 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.456-393G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222634934 | |||||||
| chr2:222635033 | T | C | 1 | a0002c0002t0004g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.456-492A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635033 | |||||||
| chr2:222635034 | C | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.456-493G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635034 | |||||||
| chr2:222635077 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.456-536C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635077 | |||||||
| chr2:222635160 | A | T | 5 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(2): Show |
5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.456-619T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635160 | |||||||
| chr2:222635343 | G | A | 5 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(2): Show |
5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.456-802C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635343 | |||||||
| chr2:222635351 | G | A | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.456-810C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635351 | |||||||
| chr2:222635437 | G | C | 1 | a0005c0005t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.456-896C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635437 | |||||||
| chr2:222635559 | C | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.456-1018G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635559 | |||||||
| chr2:222635821 | T | A | 9 | a0001c0001t0007g0038 a0001c0001t0007g0087 a0001c0001t0007g0134 others(6): Show |
9 | HG00280.hp2 HG00597.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.456-1280A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635821 | |||||||
| chr2:222635850 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.456-1309G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635850 | |||||||
| chr2:222635877 | C | G | 22 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(19): Show |
23 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.456-1336G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635877 | |||||||
| chr2:222635983 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.456-1442T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222635983 | |||||||
| chr2:222636176 | G | C | 3 | a0001c0001t0012g0037 a0001c0001t0012g0062 a0001c0001t0012g0063 |
3 | HG02615.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.456-1635C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636176 | |||||||
| chr2:222636279 | C | T | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.456-1738G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636279 | |||||||
| chr2:222636331 | C | T | 1 | a0002c0002t0004g0191 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.456-1790G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636331 | |||||||
| chr2:222636373 | G | A | 3 | a0001c0001t0016g0185 a0001c0001t0016g0186 a0002c0002t0006g0187 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.456-1832C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636373 | |||||||
| chr2:222636385 | C | CA | 59 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(56): Show |
62 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.456-1845dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636385 | |||||||
| chr2:222636385 | C | CAA | 37 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(34): Show |
42 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.456-1846_456-1845d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636385 | |||||||
| chr2:222636494 | CTA | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.456-1955_456-1954d others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636494 | |||||||
| chr2:222636558 | G | T | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0002g0231 |
3 | HG01169.hp1 HG01943.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.456-2017C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636558 | |||||||
| chr2:222636601 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG01175.hp2 HG01515.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-2060T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636601 | |||||||
| chr2:222636691 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.456-2150C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636691 | |||||||
| chr2:222636769 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.456-2228G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636769 | |||||||
| chr2:222636799 | A | T | 4 | a0001c0001t0008g0282 a0001c0001t0008g0285 a0001c0001t0014g0286 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-2258T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636799 | |||||||
| chr2:222636875 | T | C | 1 | a0001c0001t0032g0142 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.456-2334A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636875 | |||||||
| chr2:222636923 | C | T | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.456-2382G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636923 | |||||||
| chr2:222636968 | C | T | 1 | a0001c0001t0008g0291 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.456-2427G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222636968 | |||||||
| chr2:222637109 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.455+2471C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637109 | |||||||
| chr2:222637137 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.455+2443C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637137 | |||||||
| chr2:222637174 | G | A | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.455+2406C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637174 | |||||||
| chr2:222637220 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.455+2360T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637220 | |||||||
| chr2:222637488 | G | A | 1 | a0001c0001t0002g0260 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.455+2092C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637488 | |||||||
| chr2:222637510 | G | A | 2 | a0002c0002t0004g0015 a0002c0002t0004g0205 |
3 | HG02717.hp1 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.455+2070C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637510 | |||||||
| chr2:222637564 | T | C | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.455+2016A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637564 | |||||||
| chr2:222637828 | T | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.455+1752A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637828 | |||||||
| chr2:222637884 | G | A | 2 | a0002c0002t0006g0175 a0002c0002t0006g0176 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.455+1696C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637884 | |||||||
| chr2:222637961 | A | G | 4 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG01069.hp1 NA18973.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.455+1619T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222637961 | |||||||
| chr2:222638127 | A | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.455+1453T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638127 | |||||||
| chr2:222638179 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.455+1401G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638179 | |||||||
| chr2:222638224 | A | T | 1 | a0001c0001t0007g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.455+1356T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638224 | |||||||
| chr2:222638651 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.455+929G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638651 | |||||||
| chr2:222638729 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.455+851T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638729 | |||||||
| chr2:222638979 | G | A | 1 | a0001c0001t0015g0043 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.455+601C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222638979 | |||||||
| chr2:222639320 | T | C | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.455+260A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 5/16 | chr2 | 222639320 | |||||||
| chr2:222639884 | A | G | 19 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(16): Show |
20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.340-189T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222639884 | |||||||
| chr2:222640108 | T | C | 11 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(8): Show |
11 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-413A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640108 | |||||||
| chr2:222640203 | G | T | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.340-508C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640203 | |||||||
| chr2:222640428 | T | C | 1 | a0001c0001t0005g0318 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.339+434A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640428 | |||||||
| chr2:222640498 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.339+364A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640498 | |||||||
| chr2:222640508 | C | G | 2 | a0002c0002t0004g0189 a0002c0002t0004g0190 |
2 | NA18955.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.339+354G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640508 | |||||||
| chr2:222640671 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.339+191T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640671 | |||||||
| chr2:222640754 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.339+108A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 4/16 | chr2 | 222640754 | |||||||
| chr2:222640997 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.270-66A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222640997 | |||||||
| chr2:222641010 | G | A | 3 | a0002c0002t0004g0206 a0002c0002t0004g0207 a0002c0002t0004g0208 |
3 | HG01192.hp2 HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.270-79C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641010 | |||||||
| chr2:222641088 | C | A | 1 | a0001c0001t0002g0222 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.270-157G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641088 | |||||||
| chr2:222641089 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.270-158T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641089 | |||||||
| chr2:222641089 | A | G | 1 | a0001c0001t0005g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.270-158T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641089 | |||||||
| chr2:222641153 | T | C | 66 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(63): Show |
73 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.270-222A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641153 | |||||||
| chr2:222641214 | C | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0224 a0001c0001t0002g0225 |
4 | HG00609.hp2 NA18981.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-283G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641214 | |||||||
| chr2:222641532 | A | T | 1 | a0002c0002t0004g0188 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.270-601T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641532 | |||||||
| chr2:222641732 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.270-801A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641732 | |||||||
| chr2:222641862 | C | G | 1 | a0001c0001t0008g0284 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.270-931G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641862 | |||||||
| chr2:222641863 | C | G | 18 | a0001c0001t0005g0306 a0001c0001t0005g0307 a0001c0001t0005g0309 others(15): Show |
20 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.270-932G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641863 | |||||||
| chr2:222641883 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.270-952G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641883 | |||||||
| chr2:222641926 | TGAA | T | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.269+922_269+924del others(3): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641926 | |||||||
| chr2:222641991 | G | C | 1 | a0001c0001t0003g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.269+860C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222641991 | |||||||
| chr2:222642003 | CT | C | 300 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(297): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.269+847delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642003 | |||||||
| chr2:222642004 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.269+847A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642004 | |||||||
| chr2:222642104 | C | T | 19 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0308 others(16): Show |
20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.269+747G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642104 | |||||||
| chr2:222642135 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.269+716C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642135 | |||||||
| chr2:222642193 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.269+658C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642193 | |||||||
| chr2:222642540 | C | G | 1 | a0001c0001t0015g0043 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.269+311G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642540 | |||||||
| chr2:222642573 | C | A | 1 | a0002c0002t0004g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.269+278G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642573 | |||||||
| chr2:222642742 | C | T | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.269+109G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 3/16 | chr2 | 222642742 | |||||||
| chr2:222643114 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.115-109A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222643114 | |||||||
| chr2:222643199 | T | C | 2 | a0001c0001t0002g0275 a0001c0001t0002g0276 |
2 | NA19009.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.115-194A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222643199 | |||||||
| chr2:222643664 | ACAGT | A | 4 | a0001c0001t0001g0145 a0001c0001t0001g0156 a0001c0001t0002g0261 others(1): Show |
4 | HG00597.hp1 NA18957.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-663_115-660del others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222643664 | |||||||
| chr2:222643713 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.115-708T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222643713 | |||||||
| chr2:222644418 | G | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.115-1413C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644418 | |||||||
| chr2:222644502 | T | G | 32 | a0002c0002t0004g0013 a0002c0002t0004g0014 a0002c0002t0004g0015 others(29): Show |
35 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.115-1497A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644502 | |||||||
| chr2:222644594 | C | T | 8 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0090 others(5): Show |
8 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-1589G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644594 | |||||||
| chr2:222644596 | G | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-1591C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644596 | |||||||
| chr2:222644800 | G | C | 2 | a0001c0001t0016g0185 a0001c0001t0016g0186 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.115-1795C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644800 | |||||||
| chr2:222644929 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.115-1924C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644929 | |||||||
| chr2:222644984 | CA | C | 81 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(78): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.115-1980delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222644984 | |||||||
| chr2:222645106 | T | A | 238 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.115-2101A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645106 | |||||||
| chr2:222645127 | G | C | 3 | a0001c0001t0016g0185 a0001c0001t0016g0186 a0002c0002t0006g0187 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.115-2122C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645127 | |||||||
| chr2:222645252 | C | A | 1 | a0001c0001t0008g0291 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.115-2247G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645252 | |||||||
| chr2:222645423 | A | G | 66 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(63): Show |
73 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.115-2418T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645423 | |||||||
| chr2:222645501 | T | G | 30 | a0002c0002t0004g0013 a0002c0002t0004g0014 a0002c0002t0004g0015 others(27): Show |
33 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.115-2496A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645501 | |||||||
| chr2:222645542 | T | C | 76 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(73): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.115-2537A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645542 | |||||||
| chr2:222645615 | CT | C | 81 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(78): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.115-2611delA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645615 | |||||||
| chr2:222645675 | T | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.115-2670A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645675 | |||||||
| chr2:222645724 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(234): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.115-2719T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645724 | |||||||
| chr2:222645927 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.114+2813G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222645927 | |||||||
| chr2:222646085 | C | T | 1 | a0001c0001t0007g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114+2655G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646085 | |||||||
| chr2:222646180 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG00673.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.114+2560A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646180 | |||||||
| chr2:222646208 | G | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.114+2532C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646208 | |||||||
| chr2:222646227 | A | G | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114+2513T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646227 | |||||||
| chr2:222646329 | ATCT | A | 32 | a0002c0002t0004g0013 a0002c0002t0004g0014 a0002c0002t0004g0015 others(29): Show |
35 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.114+2408_114+2410d others(5): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646329 | |||||||
| chr2:222646377 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.114+2363G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646377 | |||||||
| chr2:222646538 | T | A | 15 | a0001c0001t0001g0266 a0001c0001t0002g0019 a0001c0001t0002g0020 others(12): Show |
17 | HG00438.hp1 HG02129.hp2 NA18956.hp1 others(14): Show |
intron_variant | MODIFIER | c.114+2202A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646538 | |||||||
| chr2:222646731 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+2009G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646731 | |||||||
| chr2:222646789 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1951G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646789 | |||||||
| chr2:222646949 | G | A | 19 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(16): Show |
20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.114+1791C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222646949 | |||||||
| chr2:222647032 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.114+1708A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647032 | |||||||
| chr2:222647071 | T | C | 1 | a0001c0001t0005g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.114+1669A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647071 | |||||||
| chr2:222647081 | T | C | 2 | a0002c0002t0004g0211 a0002c0002t0028g0209 |
2 | HG01257.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.114+1659A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647081 | |||||||
| chr2:222647173 | T | C | 1 | a0002c0002t0004g0210 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114+1567A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647173 | |||||||
| chr2:222647231 | G | T | 1 | a0001c0001t0002g0221 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.114+1509C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647231 | |||||||
| chr2:222647523 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.114+1217G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647523 | |||||||
| chr2:222647589 | G | A | 2 | a0001c0001t0003g0077 a0001c0001t0003g0078 |
2 | HG00639.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.114+1151C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647589 | |||||||
| chr2:222647626 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+1114T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647626 | |||||||
| chr2:222647660 | G | C | 1 | a0001c0001t0002g0277 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.114+1080C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647660 | |||||||
| chr2:222647721 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+1019G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647721 | |||||||
| chr2:222647726 | T | C | 19 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(16): Show |
20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.114+1014A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647726 | |||||||
| chr2:222647797 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+943C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647797 | |||||||
| chr2:222647941 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.114+799A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222647941 | |||||||
| chr2:222648008 | A | G | 1 | a0001c0001t0002g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.114+732T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648008 | |||||||
| chr2:222648127 | T | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.114+613A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648127 | |||||||
| chr2:222648247 | G | A | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+493C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648247 | |||||||
| chr2:222648365 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+375C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648365 | |||||||
| chr2:222648426 | C | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+314G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648426 | |||||||
| chr2:222648636 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.114+104T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648636 | |||||||
| chr2:222648680 | CCCTGAAA others(6): Show |
C | 1 | a0001c0001t0007g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114+47_114+59delCT others(11): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 2/16 | chr2 | 222648680 | |||||||
| chr2:222648856 | T | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-61A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222648856 | |||||||
| chr2:222649008 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-213A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649008 | |||||||
| chr2:222649044 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-249G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649044 | |||||||
| chr2:222649170 | G | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-375C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649170 | |||||||
| chr2:222649175 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0158 |
3 | NA18982.hp2 NA19007.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.59-380C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649175 | |||||||
| chr2:222649234 | TA | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.59-440delT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649234 | |||||||
| chr2:222649234 | TAA | T | 69 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(66): Show |
76 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.59-441_59-440delTT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649234 | |||||||
| chr2:222649247 | A | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-452T>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649247 | |||||||
| chr2:222649263 | G | A | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-468C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649263 | |||||||
| chr2:222649491 | T | C | 5 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(2): Show |
5 | HG01109.hp2 HG01928.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-696A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649491 | |||||||
| chr2:222649695 | C | G | 3 | a0001c0001t0003g0039 a0001c0001t0021g0040 a0001c0001t0022g0041 |
3 | HG00140.hp2 HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.59-900G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649695 | |||||||
| chr2:222649796 | T | G | 1 | a0001c0001t0003g0032 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.59-1001A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649796 | |||||||
| chr2:222649920 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-1125A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222649920 | |||||||
| chr2:222650235 | G | C | 12 | a0002c0002t0006g0011 a0002c0002t0006g0174 a0002c0002t0006g0175 others(9): Show |
14 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-1440C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650235 | |||||||
| chr2:222650313 | G | C | 1 | a0002c0002t0004g0212 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.59-1518C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650313 | |||||||
| chr2:222650417 | G | A | 1 | a0002c0002t0006g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.59-1622C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650417 | |||||||
| chr2:222650530 | T | C | 2 | a0002c0002t0006g0213 a0002c0002t0006g0214 |
2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.59-1735A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650530 | |||||||
| chr2:222650578 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-1783A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650578 | |||||||
| chr2:222650650 | C | T | 3 | a0002c0002t0006g0174 a0002c0002t0006g0175 a0002c0002t0006g0176 |
3 | HG02451.hp1 HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.59-1855G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650650 | |||||||
| chr2:222650846 | T | C | 19 | a0001c0001t0005g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 others(16): Show |
20 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-2051A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650846 | |||||||
| chr2:222650907 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.59-2112T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222650907 | |||||||
| chr2:222651192 | C | A | 3 | a0001c0001t0016g0185 a0001c0001t0016g0186 a0002c0002t0006g0187 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.59-2397G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651192 | |||||||
| chr2:222651338 | A | G | 76 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(73): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.59-2543T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651338 | |||||||
| chr2:222651646 | T | C | 1 | a0002c0002t0006g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.59-2851A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651646 | |||||||
| chr2:222651753 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.59-2958G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651753 | |||||||
| chr2:222651755 | T | C | 1 | a0001c0001t0003g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.59-2960A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651755 | |||||||
| chr2:222651891 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.59-3096A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222651891 | |||||||
| chr2:222652045 | T | A | 81 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(78): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.59-3250A>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652045 | |||||||
| chr2:222652059 | G | A | 1 | a0002c0002t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.59-3264C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652059 | |||||||
| chr2:222652106 | G | A | 1 | a0001c0001t0003g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-3311C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652106 | |||||||
| chr2:222652333 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.59-3538C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652333 | |||||||
| chr2:222652415 | T | G | 1 | a0001c0001t0002g0278 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.58+3601A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652415 | |||||||
| chr2:222652458 | T | C | 1 | a0001c0001t0003g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.58+3558A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652458 | |||||||
| chr2:222652540 | C | T | 59 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(56): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.58+3476G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652540 | |||||||
| chr2:222652584 | G | A | 2 | a0001c0001t0018g0279 a0001c0001t0018g0280 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.58+3432C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652584 | |||||||
| chr2:222652619 | A | C | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3397T>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652619 | |||||||
| chr2:222652621 | C | T | 1 | a0001c0001t0007g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.58+3395G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652621 | |||||||
| chr2:222652983 | T | C | 1 | a0002c0002t0004g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+3033A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652983 | |||||||
| chr2:222652986 | C | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.58+3030G>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222652986 | |||||||
| chr2:222653015 | A | G | 1 | a0001c0001t0012g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58+3001T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653015 | |||||||
| chr2:222653070 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.58+2946G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653070 | |||||||
| chr2:222653160 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 |
3 | HG02258.hp2 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.58+2856T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653160 | |||||||
| chr2:222653229 | A | G | 1 | a0001c0001t0017g0183 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58+2787T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653229 | |||||||
| chr2:222653355 | TAAAG | T | 15 | a0002c0002t0006g0011 a0002c0002t0006g0171 a0002c0002t0006g0174 others(12): Show |
17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+2657_58+2660del others(4): Show |
FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653355 | |||||||
| chr2:222653431 | G | GA | 10 | a0001c0001t0008g0282 a0001c0001t0008g0284 a0001c0001t0008g0285 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+2584dupT | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653431 | |||||||
| chr2:222653432 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(169): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.58+2584T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653432 | |||||||
| chr2:222653507 | A | G | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+2509T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653507 | |||||||
| chr2:222653630 | A | AT | 23 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0005g0304 others(20): Show |
24 | HG00639.hp2 HG00735.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.58+2385dupA | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653630 | |||||||
| chr2:222653691 | C | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+2325G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653691 | |||||||
| chr2:222653733 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
164 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.58+2283G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653733 | |||||||
| chr2:222653783 | A | G | 1 | a0001c0001t0019g0170 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.58+2233T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222653783 | |||||||
| chr2:222654046 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.58+1970C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654046 | |||||||
| chr2:222654088 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1928G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654088 | |||||||
| chr2:222654172 | G | A | 2 | a0002c0002t0006g0295 a0002c0002t0006g0296 |
2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.58+1844C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654172 | |||||||
| chr2:222654178 | C | T | 1 | a0001c0001t0002g0169 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.58+1838G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654178 | |||||||
| chr2:222654249 | C | T | 10 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0025 others(7): Show |
12 | HG00438.hp2 HG00609.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+1767G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654249 | |||||||
| chr2:222654509 | A | G | 3 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0002g0168 |
3 | HG02074.hp1 NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.58+1507T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654509 | |||||||
| chr2:222654611 | T | C | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+1405A>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654611 | |||||||
| chr2:222654711 | T | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.58+1305A>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222654711 | |||||||
| chr2:222655171 | G | A | 2 | a0002c0002t0006g0295 a0002c0002t0006g0296 |
2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.58+845C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655171 | |||||||
| chr2:222655235 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.58+781C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655235 | |||||||
| chr2:222655410 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.58+606T>C | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655410 | |||||||
| chr2:222655465 | C | T | 4 | a0001c0001t0011g0298 a0001c0001t0011g0299 a0001c0001t0011g0300 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+551G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655465 | |||||||
| chr2:222655496 | C | A | 7 | a0001c0001t0005g0310 a0001c0001t0005g0311 a0001c0001t0005g0312 others(4): Show |
7 | HG01361.hp1 HG01975.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+520G>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655496 | |||||||
| chr2:222655500 | G | A | 2 | a0001c0001t0005g0316 a0001c0001t0005g0317 |
2 | NA18960.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.58+516C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655500 | |||||||
| chr2:222655565 | G | T | 1 | a0003c0006t0035g0297 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+451C>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655565 | |||||||
| chr2:222655568 | C | T | 152 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(149): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.58+448G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655568 | |||||||
| chr2:222655689 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.58+327G>A | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655689 | |||||||
| chr2:222655755 | G | A | 1 | a0001c0001t0005g0318 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.58+261C>T | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655755 | |||||||
| chr2:222655800 | G | C | 1 | a0001c0001t0020g0021 | 2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.58+216C>G | FARSB | ENSG00000116120.11 | transcript | ENST00000281828.8 | protein_coding | 1/16 | chr2 | 222655800 |