Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23197 |
| ensemblid | ENSG00000113194.13 |
| hgncid | 24666 |
| symbol | FAF2 |
| name | Fas associated factor family member 2 |
| refseq_nuc | NM_014613.3 |
| refseq_prot | NP_055428.1 |
| ensembl_nuc | ENST00000261942.7 |
| ensembl_prot | ENSP00000261942.6 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 176448385 |
| end | 176510074 |
| strand | + |
| ver | v1.2 |
| region | chr5:176448385-176510074 |
| region5000 | chr5:176443385-176515074 |
| regionname0 | FAF2_chr5_176448385_176510074 |
| regionname5000 | FAF2_chr5_176443385_176515074 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 445 | 365 | 84 | 64 | 166 | 10 | 39 | 127 | FAF2_chr5_176443385_176515074 | FAF2 | MAAPE others(440): Show |
chr5 | 176443385 | 176515074 |
| a0002 | 0/0 | 445 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FAF2_chr5_176443385_176515074 | FAF2 | MAAPE others(440): Show |
chr5 | 176443385 | 176515074 |
| a0003 | 0/0 | 445 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | MAAPE others(440): Show |
chr5 | 176443385 | 176515074 |
| a0004 | 0/0 | 445 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | MAAPE others(440): Show |
chr5 | 176443385 | 176515074 |
| a0005 | 0/0 | 445 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | MAAPE others(440): Show |
chr5 | 176443385 | 176515074 |
| a0006 | 0/0 | 445 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | MAAPE others(440): Show |
chr5 | 176443385 | 176515074 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1335 | 362 | 82 | 64 | 165 | 10 | 39 | FAF2_chr5_176443385_176515074 | FAF2 | ATGGC others(1330): Show |
chr5 | 176443385 | 176515074 | ||
| a0001c0005 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | ATGGC others(1330): Show |
chr5 | 176443385 | 176515074 | ||
| a0001c0008 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | ATGGC others(1330): Show |
chr5 | 176443385 | 176515074 | ||
| a0001c0009 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | ATGGC others(1330): Show |
chr5 | 176443385 | 176515074 | ||
| a0002c0002 | 0/0 | 1335 | 3 | 0 | 0 | 3 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | ATGGC others(1330): Show |
chr5 | 176443385 | 176515074 | ||
| a0003c0003 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | ATGGC others(1330): Show |
chr5 | 176443385 | 176515074 | ||
| a0004c0006 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | ATGGC others(1330): Show |
chr5 | 176443385 | 176515074 | ||
| a0005c0004 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | ATGGC others(1330): Show |
chr5 | 176443385 | 176515074 | ||
| a0006c0007 | 0/0 | 1335 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | ATGGC others(1330): Show |
chr5 | 176443385 | 176515074 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4485 | 103 | 4 | 24 | 53 | 3 | 18 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0002 | 1/0 | 4485 | 58 | 4 | 9 | 32 | 4 | 8 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0003 | 0/0 | 4486 | 56 | 1 | 10 | 36 | 0 | 9 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4481): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0004 | 0/0 | 4485 | 45 | 37 | 7 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0005 | 0/0 | 4485 | 29 | 1 | 2 | 24 | 1 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0006 | 0/0 | 4485 | 22 | 13 | 5 | 1 | 2 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0007 | 0/0 | 4487 | 7 | 4 | 3 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4482): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0008 | 0/0 | 4489 | 5 | 0 | 0 | 5 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4484): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0009 | 0/0 | 4486 | 4 | 3 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4481): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0010 | 0/0 | 4485 | 4 | 4 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0011 | 0/0 | 4485 | 3 | 0 | 0 | 3 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0012 | 0/0 | 4485 | 2 | 0 | 0 | 2 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0013 | 0/0 | 4485 | 2 | 2 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0014 | 0/0 | 4485 | 2 | 2 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0015 | 0/0 | 4486 | 2 | 0 | 0 | 2 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4481): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0016 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0017 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0018 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0019 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0020 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4481): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0021 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0022 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0023 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0024 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0025 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0026 | 0/0 | 4486 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4481): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0028 | 0/0 | 4486 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4481): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0029 | 0/0 | 4487 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4482): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0030 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0031 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0032 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4481): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0033 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0001t0034 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0005t0001 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0001c0008t0027 | 0/0 | 4486 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4481): Show |
chr5 | 176443385 | 176515074 |
| a0001c0009t0002 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0002c0002t0001 | 0/0 | 4485 | 3 | 0 | 0 | 3 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0003c0003t0002 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0004c0006t0004 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0005c0004t0002 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| a0006c0007t0002 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | AGGAG others(4480): Show |
chr5 | 176443385 | 176515074 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0004g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0005g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0007g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0008g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0011g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0011g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0012g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0013g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0014g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0014g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0015g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0015g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0016g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0017g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0018g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0019g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0020g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0021g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0022g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0023g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0024g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0025g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0026g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0028g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0029g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0030g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0031g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0032g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0033g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0001t0034g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0008t0027g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0001c0009t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0003c0003t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0004c0006t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0005c0004t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| a0006c0007t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0309 | EUR | FIN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0244 | EUR | FIN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0365 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0363 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0220 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0016 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0227 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0248 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0184 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0099 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0332 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01433 | hp1 | a0001 | c0001 | t0017 | g0276 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01496 | hp1 | a0001 | c0001 | t0018 | g0235 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0271 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0338 | EUR | IBS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0224 | EUR | IBS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0331 | EUR | IBS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0225 | EUR | IBS | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01891 | hp1 | a0001 | c0001 | t0024 | g0236 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01891 | hp2 | a0001 | c0001 | t0013 | g0026 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0090 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02040 | hp1 | a0001 | c0001 | t0016 | g0202 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02040 | hp2 | a0001 | c0001 | t0030 | g0201 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0251 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02056 | hp2 | a0001 | c0001 | t0029 | g0094 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0261 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0253 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0257 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02132 | hp2 | a0001 | c0001 | t0026 | g0092 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0341 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0215 | EAS | KHV | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0256 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | CDX | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CDX | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0197 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02258 | hp2 | a0004 | c0006 | t0004 | g0352 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0324 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02451 | hp1 | a0005 | c0004 | t0002 | g0350 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0246 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0279 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02602 | hp2 | a0001 | c0001 | t0031 | g0119 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0351 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0368 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0349 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0088 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0223 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0361 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0366 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02886 | hp1 | a0001 | c0001 | t0022 | g0268 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02886 | hp2 | a0001 | c0001 | t0032 | g0098 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0101 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0020 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02922 | hp2 | a0001 | c0001 | t0014 | g0015 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0367 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0209 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03130 | hp1 | a0001 | c0001 | t0034 | g0207 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0247 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0249 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0262 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0097 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0245 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0283 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03486 | hp2 | a0001 | c0008 | t0027 | g0296 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0359 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | GWD | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0360 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0333 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0342 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03942 | hp1 | a0006 | c0007 | t0002 | g0330 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04115 | hp2 | a0001 | c0001 | t0028 | g0102 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0067 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0325 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0344 | SAS | STU | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18522 | hp1 | a0001 | c0001 | t0033 | g0297 | AFR | YRI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | YRI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | CHB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | CHB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | CHB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0272 | AFR | YRI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | YRI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18942 | hp2 | a0001 | c0001 | t0012 | g0129 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0364 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18947 | hp2 | a0001 | c0001 | t0008 | g0062 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18951 | hp1 | a0001 | c0001 | t0020 | g0143 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0282 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18953 | hp2 | a0001 | c0001 | t0012 | g0126 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0260 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18965 | hp2 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18969 | hp1 | a0001 | c0001 | t0011 | g0137 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0266 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18997 | hp2 | a0001 | c0001 | t0015 | g0086 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18999 | hp2 | a0001 | c0001 | t0019 | g0326 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19004 | hp2 | a0001 | c0001 | t0008 | g0059 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19009 | hp2 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0273 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0353 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0275 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19060 | hp1 | a0001 | c0001 | t0011 | g0107 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0265 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19068 | hp2 | a0001 | c0001 | t0015 | g0087 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0269 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0362 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19077 | hp1 | a0001 | c0009 | t0002 | g0304 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19079 | hp1 | a0001 | c0001 | t0011 | g0138 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0038 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | ASW | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ASW | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0346 | EUR | TSI | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | GIH | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0216 | SAS | GIH | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01123 | hp1 | a0001 | c0001 | t0021 | g0335 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0221 | AMR | CLM | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0222 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0081 | AFR | ACB | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03471 | hp1 | a0001 | c0001 | t0023 | g0237 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | MSL | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0270 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | LWK | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0285 | REF | REF | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0321 | REF | REF | FAF2_chr5_176443385_176515074 | FAF2 | chr5 | 176443385 | 176515074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176486391 | G | A | 1 | a0003 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.169G>A | p.Val57Ile | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/11 | 192/4485 | 169/1338 | 57/445 | chr5 | 176486391 | |||
| chr5:176492223 | C | A | 1 | a0005 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.374C>A | p.Pro125His | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/11 | 397/4485 | 374/1338 | 125/445 | chr5 | 176492223 | |||
| chr5:176496501 | G | A | 1 | a0004 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.677G>A | p.Arg226Gln | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/11 | 700/4485 | 677/1338 | 226/445 | chr5 | 176496501 | |||
| chr5:176496557 | G | A | 1 | a0006 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.733G>A | p.Val245Met | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/11 | 756/4485 | 733/1338 | 245/445 | chr5 | 176496557 | |||
| chr5:176499030 | G | A | 1 | a0002 | 3 | NA18974.hp1 NA19066.hp1 NA19082.hp2 |
missense_variant | MODERATE | c.956G>A | p.Arg319Gln | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/11 | 979/4485 | 956/1338 | 319/445 | chr5 | 176499030 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176492323 | G | A | 1 | a0001c0005 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.474G>A | p.Thr158Thr | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/11 | 497/4485 | 474/1338 | 158/445 | chr5 | 176492323 | |||
| chr5:176496637 | T | G | 1 | a0001c0008 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.813T>G | p.Thr271Thr | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/11 | 836/4485 | 813/1338 | 271/445 | chr5 | 176496637 | |||
| chr5:176498989 | G | A | 1 | a0001c0009 | 1 | NA19077.hp1 | synonymous_variant | LOW | c.915G>A | p.Gln305Gln | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/11 | 938/4485 | 915/1338 | 305/445 | chr5 | 176498989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176507052 | A | ATAT | 1 | a0001c0001t0008 | 5 | NA18947.hp2 NA18965.hp2 NA19004.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*118_*120dupTAT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 121 | INFO_REALIGN_3_PRIME | chr5 | 176507052 | |||||
| chr5:176507231 | T | C | 1 | a0001c0001t0016 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*281T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 281 | chr5 | 176507231 | ||||||
| chr5:176507255 | C | T | 1 | a0001c0001t0011 | 3 | NA18969.hp1 NA19060.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*305C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 305 | chr5 | 176507255 | ||||||
| chr5:176507526 | A | AT | 1 | a0001c0001t0007 | 7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*583dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 584 | INFO_REALIGN_3_PRIME | chr5 | 176507526 | |||||
| chr5:176507528 | T | A | 1 | a0001c0001t0017 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 578 | chr5 | 176507528 | ||||||
| chr5:176507588 | C | T | 1 | a0001c0001t0034 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 638 | chr5 | 176507588 | ||||||
| chr5:176507621 | G | A | 1 | a0001c0001t0018 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 671 | chr5 | 176507621 | ||||||
| chr5:176507774 | A | G | 1 | a0001c0001t0033 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*824A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 824 | chr5 | 176507774 | ||||||
| chr5:176508024 | C | T | 1 | a0001c0001t0032 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1074C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1074 | chr5 | 176508024 | ||||||
| chr5:176508058 | T | C | 1 | a0001c0001t0019 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1108T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1108 | chr5 | 176508058 | ||||||
| chr5:176508140 | C | G | 1 | a0001c0001t0031 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1190C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1190 | chr5 | 176508140 | ||||||
| chr5:176508144 | C | A | 1 | a0001c0001t0031 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1194C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1194 | chr5 | 176508144 | ||||||
| chr5:176508315 | T | C | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(21): Show |
228 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*1365T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1365 | chr5 | 176508315 | ||||||
| chr5:176508392 | C | CA | 9 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(6): Show |
75 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1442_*1443insA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1443 | chr5 | 176508392 | ||||||
| chr5:176508577 | T | C | 1 | a0001c0001t0012 | 2 | NA18942.hp2 NA18953.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1627T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1627 | chr5 | 176508577 | ||||||
| chr5:176508728 | C | T | 32 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(29): Show |
305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*1778C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1778 | chr5 | 176508728 | ||||||
| chr5:176508734 | A | G | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0017 others(1): Show |
53 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1784A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1784 | chr5 | 176508734 | ||||||
| chr5:176508858 | C | T | 4 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0014 others(1): Show |
9 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1908C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1908 | chr5 | 176508858 | ||||||
| chr5:176508872 | A | G | 1 | a0001c0001t0025 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1922A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 1922 | chr5 | 176508872 | ||||||
| chr5:176508959 | A | AT | 3 | a0001c0001t0009 a0001c0001t0029 a0001c0001t0032 |
6 | HG01243.hp1 HG02056.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2019dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2020 | INFO_REALIGN_3_PRIME | chr5 | 176508959 | |||||
| chr5:176509121 | T | C | 2 | a0001c0001t0015 a0001c0001t0026 |
3 | HG02132.hp2 NA18997.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2171T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2171 | chr5 | 176509121 | ||||||
| chr5:176509208 | C | T | 1 | a0001c0001t0024 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2258C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2258 | chr5 | 176509208 | ||||||
| chr5:176509209 | G | C | 3 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0032 |
7 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2259G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2259 | chr5 | 176509209 | ||||||
| chr5:176509316 | C | A | 2 | a0001c0001t0005 a0001c0001t0017 |
30 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2366C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2366 | chr5 | 176509316 | ||||||
| chr5:176509515 | T | C | 10 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(7): Show |
116 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*2565T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2565 | chr5 | 176509515 | ||||||
| chr5:176509527 | G | A | 1 | a0001c0008t0027 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2577G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2577 | chr5 | 176509527 | ||||||
| chr5:176509579 | T | C | 1 | a0001c0001t0030 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2629T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2629 | chr5 | 176509579 | ||||||
| chr5:176509617 | G | C | 1 | a0001c0001t0022 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2667 | chr5 | 176509617 | ||||||
| chr5:176509749 | T | C | 1 | a0001c0001t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2799T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2799 | chr5 | 176509749 | ||||||
| chr5:176509763 | A | G | 1 | a0001c0001t0028 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2813A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 11/11 | 2813 | chr5 | 176509763 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:176448562 | A | C | 1 | a0001c0001t0004g0368 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.63+92A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448562 | |||||||
| chr5:176448651 | C | T | 2 | a0001c0001t0007g0366 a0001c0001t0007g0367 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63+181C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448651 | |||||||
| chr5:176448671 | G | C | 25 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(22): Show |
26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+201G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448671 | |||||||
| chr5:176448673 | A | G | 4 | a0001c0001t0005g0362 a0001c0001t0005g0363 a0001c0001t0005g0364 others(1): Show |
4 | HG00438.hp1 HG00609.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+203A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448673 | |||||||
| chr5:176448797 | T | C | 2 | a0001c0001t0010g0005 a0001c0001t0010g0006 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.63+327T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448797 | |||||||
| chr5:176448800 | A | G | 1 | a0001c0001t0010g0006 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.63+330A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448800 | |||||||
| chr5:176448916 | G | T | 1 | a0001c0001t0003g0361 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.63+446G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448916 | |||||||
| chr5:176448960 | G | A | 1 | a0001c0001t0005g0027 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.63+490G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176448960 | |||||||
| chr5:176449077 | C | T | 1 | a0001c0001t0001g0360 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.63+607C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449077 | |||||||
| chr5:176449097 | C | T | 1 | a0001c0001t0004g0368 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.63+627C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449097 | |||||||
| chr5:176449143 | A | G | 2 | a0001c0001t0001g0359 a0001c0001t0001g0360 |
2 | HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.63+673A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449143 | |||||||
| chr5:176449420 | C | A | 69 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(66): Show |
70 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+950C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449420 | |||||||
| chr5:176449461 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.63+991G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449461 | |||||||
| chr5:176449596 | C | T | 4 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(1): Show |
4 | NA18955.hp2 NA18990.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1126C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449596 | |||||||
| chr5:176449713 | TATTGATA others(69): Show |
T | 1 | a0001c0001t0001g0354 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.63+1244_63+1319del others(76): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176449713 | |||||||
| chr5:176450055 | A | ACAGTTGA others(45): Show |
1 | a0001c0001t0002g0096 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.63+1586_63+1637dup others(52): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176450055 | ||||||
| chr5:176450109 | C | G | 1 | a0001c0001t0013g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.63+1639C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450109 | |||||||
| chr5:176450268 | T | C | 3 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 |
3 | NA18971.hp2 NA19054.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.63+1798T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450268 | |||||||
| chr5:176450318 | A | G | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+1848A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450318 | |||||||
| chr5:176450413 | CAT | C | 3 | a0001c0001t0004g0022 a0001c0001t0010g0005 a0001c0001t0010g0006 |
3 | HG02257.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.63+1944_63+1945del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450413 | |||||||
| chr5:176450556 | C | CT | 7 | a0001c0001t0004g0353 a0001c0001t0007g0366 a0001c0001t0007g0367 others(4): Show |
7 | HG02056.hp2 HG02280.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+2100dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176450556 | ||||||
| chr5:176450583 | C | T | 4 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+2113C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450583 | |||||||
| chr5:176450788 | C | T | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+2318C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450788 | |||||||
| chr5:176450955 | A | G | 1 | a0004c0006t0004g0352 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63+2485A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176450955 | |||||||
| chr5:176451006 | G | A | 296 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(293): Show |
299 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(296): Show |
intron_variant | MODIFIER | c.63+2536G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451006 | |||||||
| chr5:176451006 | G | T | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+2536G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451006 | |||||||
| chr5:176451313 | G | A | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+2843G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451313 | |||||||
| chr5:176451326 | G | T | 2 | a0001c0001t0004g0003 a0004c0006t0004g0352 |
3 | HG02258.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.63+2856G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451326 | |||||||
| chr5:176451414 | G | A | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+2944G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451414 | |||||||
| chr5:176451450 | T | C | 301 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(298): Show |
304 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(301): Show |
intron_variant | MODIFIER | c.63+2980T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451450 | |||||||
| chr5:176451726 | GAT | G | 3 | a0001c0001t0001g0286 a0001c0001t0007g0366 a0001c0001t0007g0367 |
3 | HG02809.hp2 HG03041.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.63+3267_63+3268del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451726 | ||||||
| chr5:176451765 | CATAT | C | 64 | a0001c0001t0002g0096 a0001c0001t0003g0002 a0001c0001t0003g0028 others(61): Show |
65 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.63+3301_63+3304del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451765 | ||||||
| chr5:176451770 | ATATACG | A | 7 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0031 others(4): Show |
7 | HG00558.hp2 NA18942.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+3302_63+3307del others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451770 | ||||||
| chr5:176451775 | CGT | C | 23 | a0001c0001t0001g0095 a0001c0001t0001g0213 a0001c0001t0001g0214 others(20): Show |
23 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+3316_63+3317del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451775 | ||||||
| chr5:176451777 | T | C | 7 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0031 others(4): Show |
7 | HG00558.hp2 NA18942.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+3307T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451777 | |||||||
| chr5:176451784 | GTGTATAT others(25): Show |
G | 64 | a0001c0001t0002g0096 a0001c0001t0003g0002 a0001c0001t0003g0028 others(61): Show |
65 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.63+3316_63+3347del others(32): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451784 | ||||||
| chr5:176451786 | G | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3316G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451786 | |||||||
| chr5:176451797 | T | C | 2 | a0001c0001t0010g0019 a0001c0001t0010g0021 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.63+3327T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451797 | |||||||
| chr5:176451799 | CAT | C | 12 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0222 others(9): Show |
12 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+3339_63+3340del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451799 | ||||||
| chr5:176451801 | TATATATA others(39): Show |
T | 1 | a0001c0001t0010g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+3345_63+3390del others(46): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451801 | ||||||
| chr5:176451803 | TATATATA others(37): Show |
T | 3 | a0001c0001t0004g0022 a0001c0001t0010g0006 a0001c0001t0013g0026 |
3 | HG01891.hp2 HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.63+3341_63+3384del others(44): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451803 | ||||||
| chr5:176451807 | TATAC | T | 6 | a0001c0001t0002g0287 a0001c0001t0002g0288 a0001c0001t0004g0023 others(3): Show |
6 | HG02965.hp1 HG03209.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3339_63+3342del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451807 | ||||||
| chr5:176451809 | T | C | 1 | a0001c0001t0006g0215 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.63+3339T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451809 | |||||||
| chr5:176451809 | TACACACA others(27): Show |
T | 23 | a0001c0001t0004g0279 a0001c0001t0004g0280 a0001c0001t0005g0027 others(20): Show |
23 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+3345_63+3378del others(34): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451809 | ||||||
| chr5:176451811 | C | CACATATA others(197): Show |
1 | a0001c0001t0001g0234 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(204): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | ||||||
| chr5:176451811 | C | CACATATA others(171): Show |
1 | a0001c0001t0001g0231 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(178): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | ||||||
| chr5:176451811 | C | CACATATA others(173): Show |
1 | a0001c0001t0001g0230 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(180): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | ||||||
| chr5:176451811 | C | CACATATA others(147): Show |
1 | a0001c0001t0001g0241 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(154): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | ||||||
| chr5:176451811 | C | CACATATA others(173): Show |
3 | a0001c0001t0001g0228 a0001c0001t0004g0233 a0001c0001t0018g0235 |
3 | HG01496.hp1 HG02055.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.63+3344_63+3345ins others(180): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | ||||||
| chr5:176451811 | C | CACATATA others(199): Show |
2 | a0001c0001t0001g0229 a0001c0001t0001g0232 |
2 | HG01257.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.63+3344_63+3345ins others(206): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | ||||||
| chr5:176451811 | C | CACATATA others(172): Show |
1 | a0001c0001t0001g0354 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(179): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451811 | ||||||
| chr5:176451811 | C | T | 16 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0031 others(13): Show |
16 | HG00558.hp2 HG00733.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+3341C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451811 | |||||||
| chr5:176451813 | C | CATATATA others(13): Show |
1 | a0001c0001t0010g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(20): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451813 | ||||||
| chr5:176451813 | C | CATATATA others(3): Show |
1 | a0001c0001t0004g0353 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451813 | ||||||
| chr5:176451813 | C | CATATATA others(171): Show |
1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.63+3344_63+3345ins others(178): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451813 | ||||||
| chr5:176451813 | CACAT | C | 32 | a0001c0001t0003g0093 a0001c0001t0004g0003 a0001c0001t0004g0238 others(29): Show |
33 | HG01167.hp1 HG01361.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.63+3345_63+3348del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451813 | ||||||
| chr5:176451815 | C | T | 126 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0110 others(123): Show |
127 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.63+3345C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451815 | |||||||
| chr5:176451815 | CAT | C | 6 | a0001c0001t0002g0312 a0001c0001t0002g0320 a0001c0001t0002g0329 others(3): Show |
6 | HG01515.hp1 HG01517.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3357_63+3358del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451815 | ||||||
| chr5:176451815 | CATAT | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0034 |
3 | NA18975.hp2 NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.63+3355_63+3358del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451815 | ||||||
| chr5:176451817 | T | C | 7 | a0001c0001t0001g0104 a0001c0001t0002g0287 a0001c0001t0002g0288 others(4): Show |
7 | HG00639.hp2 HG02280.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+3347T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451817 | |||||||
| chr5:176451817 | T | TATATATA others(197): Show |
1 | a0001c0001t0001g0108 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(204): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451817 | ||||||
| chr5:176451817 | T | TATATATA others(159): Show |
1 | a0001c0001t0001g0286 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(166): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451817 | ||||||
| chr5:176451817 | T | TATATATA others(171): Show |
1 | a0001c0001t0001g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(178): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451817 | ||||||
| chr5:176451817 | T | TATATATA others(145): Show |
2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA18944.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(152): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451817 | ||||||
| chr5:176451817 | T | TATATATA others(29): Show |
4 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(36): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451817 | ||||||
| chr5:176451819 | T | TATACACA others(39): Show |
1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63+3352_63+3353ins others(46): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATACACA others(65): Show |
1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.63+3352_63+3353ins others(72): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATACATA others(217): Show |
1 | a0001c0001t0004g0105 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.63+3352_63+3353ins others(224): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATACATA others(143): Show |
1 | a0001c0001t0001g0106 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.63+3352_63+3353ins others(150): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(157): Show |
1 | a0001c0001t0011g0107 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(164): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(115): Show |
2 | a0001c0001t0001g0359 a0001c0001t0001g0360 |
2 | HG03492.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(122): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(167): Show |
1 | a0001c0001t0001g0111 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(174): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(191): Show |
1 | a0001c0001t0001g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(198): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(169): Show |
1 | a0001c0001t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(176): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(115): Show |
1 | a0001c0001t0001g0113 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(122): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(245): Show |
1 | a0001c0001t0001g0114 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(252): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(167): Show |
1 | a0001c0001t0001g0115 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(174): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(167): Show |
2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01070.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(174): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(91): Show |
1 | a0001c0001t0001g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(98): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(115): Show |
2 | a0001c0001t0004g0120 a0001c0001t0031g0119 |
2 | HG02602.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(122): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(141): Show |
1 | a0001c0001t0001g0121 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(148): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(193): Show |
1 | a0001c0001t0001g0122 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(200): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(117): Show |
8 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0130 others(5): Show |
8 | HG01109.hp2 HG01175.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(124): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(247): Show |
1 | a0001c0001t0001g0124 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(254): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(141): Show |
1 | a0001c0001t0001g0125 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(148): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(143): Show |
24 | a0001c0001t0001g0095 a0001c0001t0001g0134 a0001c0001t0001g0135 others(21): Show |
24 | HG00642.hp1 HG00733.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(150): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(193): Show |
1 | a0001c0001t0001g0133 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(200): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(169): Show |
20 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(17): Show |
20 | HG00735.hp1 HG01074.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(176): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(195): Show |
17 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(14): Show |
17 | HG00423.hp2 HG00609.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(202): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(219): Show |
1 | a0001c0001t0001g0174 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(226): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(221): Show |
3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG01257.hp1 HG01258.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(228): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(247): Show |
1 | a0001c0001t0001g0195 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(254): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(273): Show |
2 | a0001c0001t0001g0196 a0001c0005t0001g0197 |
2 | HG01952.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(280): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(299): Show |
1 | a0001c0001t0004g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(306): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(155): Show |
1 | a0001c0001t0004g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(162): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451819 | T | TATATACA others(119): Show |
2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | NA18960.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(126): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451819 | ||||||
| chr5:176451821 | T | TATACATA others(63): Show |
1 | a0001c0001t0004g0212 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(70): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | ||||||
| chr5:176451821 | T | TATACATA others(139): Show |
1 | a0001c0001t0001g0118 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(146): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | ||||||
| chr5:176451821 | T | TATACATA others(89): Show |
1 | a0001c0001t0034g0207 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(96): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | ||||||
| chr5:176451821 | T | TATACATA others(141): Show |
1 | a0001c0001t0004g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(148): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | ||||||
| chr5:176451821 | T | TATACATA others(167): Show |
2 | a0001c0001t0016g0202 a0001c0001t0030g0201 |
2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(174): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | ||||||
| chr5:176451821 | T | TATACATA others(191): Show |
1 | a0001c0001t0001g0153 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(198): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | ||||||
| chr5:176451821 | T | TATACATA others(193): Show |
1 | a0001c0001t0001g0200 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(200): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | ||||||
| chr5:176451821 | T | TATACATA others(219): Show |
1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(226): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | ||||||
| chr5:176451821 | T | TATACATA others(195): Show |
1 | a0001c0001t0001g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.63+3354_63+3355ins others(202): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451821 | ||||||
| chr5:176451823 | T | TACATATA others(61): Show |
3 | a0001c0001t0004g0209 a0001c0001t0004g0210 a0001c0001t0004g0211 |
3 | HG02965.hp2 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.63+3354_63+3355ins others(68): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451823 | ||||||
| chr5:176451825 | T | C | 8 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0033 others(5): Show |
8 | HG02135.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+3355T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451825 | |||||||
| chr5:176451827 | T | C | 36 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(33): Show |
37 | HG00408.hp2 HG00438.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.63+3357T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451827 | |||||||
| chr5:176451827 | TAC | T | 3 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0033 |
3 | NA18942.hp1 NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.63+3359_63+3360del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451827 | ||||||
| chr5:176451829 | C | T | 142 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0110 others(139): Show |
142 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.63+3359C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451829 | |||||||
| chr5:176451829 | CAT | C | 8 | a0001c0001t0001g0241 a0001c0001t0004g0003 a0001c0001t0004g0238 others(5): Show |
9 | HG01891.hp1 HG01928.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+3371_63+3372del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451829 | ||||||
| chr5:176451830 | A | G | 1 | a0001c0001t0006g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+3360A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451830 | |||||||
| chr5:176451831 | T | C | 124 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0110 others(121): Show |
126 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(123): Show |
intron_variant | MODIFIER | c.63+3361T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451831 | |||||||
| chr5:176451831 | T | TATATATA others(3): Show |
1 | a0001c0001t0004g0353 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+3370_63+3371ins others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451831 | ||||||
| chr5:176451832 | ATATATAT others(64): Show |
A | 1 | a0001c0001t0003g0037 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.63+3364_63+3434del others(71): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451832 | ||||||
| chr5:176451833 | T | C | 14 | a0001c0001t0001g0118 a0001c0001t0001g0153 a0001c0001t0001g0199 others(11): Show |
14 | HG02040.hp1 HG02040.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.63+3363T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451833 | |||||||
| chr5:176451833 | T | TATACAC | 4 | a0001c0001t0004g0217 a0001c0001t0004g0218 a0001c0001t0004g0219 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3366_63+3367ins others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451833 | ||||||
| chr5:176451837 | TATATACA others(3): Show |
T | 1 | a0001c0001t0004g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.63+3373_63+3382del others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451837 | ||||||
| chr5:176451837 | TATATACA others(31): Show |
T | 3 | a0001c0001t0004g0012 a0001c0001t0014g0014 a0001c0001t0014g0015 |
3 | HG02922.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+3373_63+3410del others(38): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451837 | ||||||
| chr5:176451839 | TATAC | T | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3371_63+3374del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451839 | ||||||
| chr5:176451839 | TATACACA others(29): Show |
T | 1 | a0001c0001t0004g0013 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+3373_63+3408del others(36): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451839 | ||||||
| chr5:176451841 | T | C | 2 | a0001c0001t0033g0297 a0001c0008t0027g0296 |
2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.63+3371T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451841 | |||||||
| chr5:176451841 | TAC | T | 65 | a0001c0001t0002g0096 a0001c0001t0003g0002 a0001c0001t0003g0028 others(62): Show |
66 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.63+3377_63+3378del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451841 | ||||||
| chr5:176451841 | TACACACA others(27): Show |
T | 3 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 |
3 | HG00733.hp1 HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.63+3373_63+3406del others(34): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451841 | ||||||
| chr5:176451843 | C | T | 36 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0104 others(33): Show |
36 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.63+3373C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451843 | |||||||
| chr5:176451845 | C | CATAT | 3 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0021 |
3 | HG02809.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.63+3376_63+3377ins others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451845 | ||||||
| chr5:176451845 | C | T | 6 | a0001c0001t0004g0007 a0001c0001t0004g0011 a0001c0001t0007g0001 others(3): Show |
7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+3375C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451845 | |||||||
| chr5:176451845 | CACATATA others(25): Show |
C | 2 | a0001c0001t0006g0215 a0001c0001t0017g0276 |
2 | HG01433.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.63+3377_63+3408del others(32): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451845 | ||||||
| chr5:176451847 | C | T | 167 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0110 others(164): Show |
169 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.63+3377C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451847 | |||||||
| chr5:176451847 | CATATATA others(25): Show |
C | 1 | a0001c0001t0004g0243 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.63+3387_63+3418del others(32): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451847 | ||||||
| chr5:176451855 | TACAC | T | 21 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0004g0023 others(18): Show |
21 | HG02055.hp1 HG02080.hp1 HG02886.hp1 others(18): Show |
intron_variant | MODIFIER | c.63+3387_63+3390del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451855 | ||||||
| chr5:176451856 | ACACATAT others(35): Show |
A | 3 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0093 |
3 | HG03834.hp2 NA18942.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.63+3387_63+3428del others(42): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451856 | |||||||
| chr5:176451856 | ACACATAT others(36): Show |
A | 1 | a0001c0001t0003g0031 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.63+3387_63+3429del others(43): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451856 | |||||||
| chr5:176451856 | ACACATAT others(39): Show |
A | 2 | a0001c0001t0004g0007 a0001c0001t0004g0011 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.63+3387_63+3432del others(46): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451856 | |||||||
| chr5:176451857 | C | T | 55 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0203 others(52): Show |
55 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.63+3387C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451857 | |||||||
| chr5:176451859 | C | CAT | 36 | a0001c0001t0001g0345 a0001c0001t0002g0004 a0001c0001t0002g0287 others(33): Show |
37 | HG00423.hp1 HG00544.hp1 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.63+3399_63+3400dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451859 | ||||||
| chr5:176451859 | C | T | 215 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(212): Show |
217 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.63+3389C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451859 | |||||||
| chr5:176451865 | TATATACA others(3): Show |
T | 1 | a0001c0001t0004g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.63+3401_63+3410del others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451865 | ||||||
| chr5:176451867 | T | C | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3397T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451867 | |||||||
| chr5:176451868 | ATACACAC others(22): Show |
A | 6 | a0001c0001t0006g0220 a0001c0001t0006g0222 a0001c0001t0006g0223 others(3): Show |
6 | HG00642.hp2 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+3400_63+3428del others(29): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | ||||||
| chr5:176451868 | ATACACAC others(23): Show |
A | 1 | a0001c0001t0006g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.63+3400_63+3429del others(30): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | ||||||
| chr5:176451868 | ATACACAC others(25): Show |
A | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.63+3400_63+3431del others(32): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | ||||||
| chr5:176451868 | ATACACAC others(26): Show |
A | 5 | a0001c0001t0004g0278 a0001c0001t0004g0281 a0001c0001t0006g0245 others(2): Show |
5 | HG02055.hp1 HG02080.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+3400_63+3432del others(33): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | ||||||
| chr5:176451868 | ATACACAC others(27): Show |
A | 2 | a0001c0001t0004g0277 a0001c0001t0005g0273 |
2 | HG03098.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.63+3400_63+3433del others(34): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | ||||||
| chr5:176451868 | ATACACAC others(28): Show |
A | 6 | a0001c0001t0005g0255 a0001c0001t0005g0259 a0001c0001t0005g0269 others(3): Show |
6 | HG03486.hp1 NA18906.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3400_63+3434del others(35): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | ||||||
| chr5:176451868 | ATACACAC others(29): Show |
A | 1 | a0001c0001t0006g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+3400_63+3435del others(36): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | ||||||
| chr5:176451868 | ATACACAC others(30): Show |
A | 3 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0006g0248 |
3 | HG01167.hp1 HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.63+3400_63+3436del others(37): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451868 | ||||||
| chr5:176451869 | T | C | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3399T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451869 | |||||||
| chr5:176451869 | T | TATAC | 4 | a0001c0001t0002g0290 a0001c0001t0002g0307 a0001c0001t0002g0308 others(1): Show |
4 | NA18955.hp1 NA18977.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+3400_63+3401ins others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451869 | ||||||
| chr5:176451870 | ACACACAT others(22): Show |
A | 1 | a0001c0001t0006g0227 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.63+3401_63+3429del others(29): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451870 | |||||||
| chr5:176451870 | ACACACAT others(26): Show |
A | 5 | a0001c0001t0006g0250 a0001c0001t0006g0270 a0001c0001t0009g0099 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+3401_63+3433del others(33): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451870 | |||||||
| chr5:176451870 | ACACACAT others(27): Show |
A | 1 | a0001c0001t0009g0101 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.63+3401_63+3434del others(34): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451870 | |||||||
| chr5:176451870 | ACACACAT others(28): Show |
A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0006g0271 |
3 | HG01496.hp2 NA18975.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.63+3401_63+3435del others(35): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451870 | |||||||
| chr5:176451871 | C | T | 241 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(238): Show |
243 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.63+3401C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451871 | |||||||
| chr5:176451873 | C | T | 9 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0203 others(6): Show |
9 | HG02015.hp2 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+3403C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451873 | |||||||
| chr5:176451875 | C | T | 17 | a0001c0001t0001g0284 a0001c0001t0002g0290 a0001c0001t0002g0307 others(14): Show |
18 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.63+3405C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451875 | |||||||
| chr5:176451877 | T | C | 25 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0115 others(22): Show |
25 | HG01256.hp2 HG01258.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.63+3407T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451877 | |||||||
| chr5:176451879 | T | C | 1 | a0001c0001t0007g0366 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.63+3409T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451879 | |||||||
| chr5:176451879 | T | TATACACA others(161): Show |
1 | a0001c0001t0005g0216 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.63+3412_63+3413ins others(168): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451879 | ||||||
| chr5:176451879 | T | TATACACA others(163): Show |
1 | a0001c0001t0004g0219 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+3412_63+3413ins others(170): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451879 | ||||||
| chr5:176451879 | T | TATATATA others(3): Show |
1 | a0001c0001t0004g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+3416_63+3417ins others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451879 | ||||||
| chr5:176451885 | T | C | 1 | a0001c0001t0001g0284 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+3415T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451885 | |||||||
| chr5:176451886 | A | G | 1 | a0001c0001t0004g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.63+3416A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451886 | |||||||
| chr5:176451886 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0009g0097 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.63+3418_63+3438del others(21): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451886 | ||||||
| chr5:176451890 | ATATTTTT others(4): Show |
A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0063 a0001c0001t0005g0090 |
3 | HG01952.hp1 NA18979.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.63+3422_63+3432del others(11): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451890 | ||||||
| chr5:176451890 | ATATTTTT others(5): Show |
A | 35 | a0001c0001t0003g0002 a0001c0001t0003g0028 a0001c0001t0003g0029 others(32): Show |
36 | HG00408.hp1 HG01167.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.63+3422_63+3433del others(12): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451890 | ||||||
| chr5:176451892 | A | AT | 6 | a0001c0001t0002g0301 a0001c0001t0002g0309 a0001c0001t0002g0315 others(3): Show |
6 | HG00280.hp1 HG01928.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+3451dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | ||||||
| chr5:176451892 | A | T | 1 | a0001c0001t0002g0302 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.63+3422A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451892 | |||||||
| chr5:176451892 | ATT | A | 16 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0115 others(13): Show |
16 | HG00609.hp2 HG00733.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+3450_63+3451del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | ||||||
| chr5:176451892 | ATTT | A | 23 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0123 others(20): Show |
23 | HG01993.hp2 HG02040.hp2 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+3449_63+3451del others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | ||||||
| chr5:176451892 | ATTTT | A | 70 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0110 others(67): Show |
70 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.63+3448_63+3451del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | ||||||
| chr5:176451892 | ATTTTT | A | 29 | a0001c0001t0001g0095 a0001c0001t0001g0114 a0001c0001t0001g0116 others(26): Show |
31 | HG00408.hp2 HG01069.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.63+3447_63+3451del others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | ||||||
| chr5:176451892 | ATTTTTT | A | 9 | a0001c0001t0001g0355 a0001c0001t0001g0357 a0001c0001t0001g0358 others(6): Show |
9 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+3446_63+3451del others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | ||||||
| chr5:176451892 | ATTTTTTT others(2): Show |
A | 23 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0280 others(20): Show |
23 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+3443_63+3451del others(9): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | ||||||
| chr5:176451892 | ATTTTTTT others(4): Show |
A | 17 | a0001c0001t0002g0096 a0001c0001t0003g0042 a0001c0001t0003g0055 others(14): Show |
17 | HG00733.hp1 HG01081.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+3441_63+3451del others(11): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | ||||||
| chr5:176451892 | ATTTTTTT others(5): Show |
A | 12 | a0001c0001t0003g0043 a0001c0001t0003g0048 a0001c0001t0003g0050 others(9): Show |
12 | HG00558.hp1 HG00621.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+3440_63+3451del others(12): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176451892 | ||||||
| chr5:176451893 | T | TA | 10 | a0001c0001t0002g0288 a0001c0001t0002g0306 a0001c0001t0002g0311 others(7): Show |
10 | HG01081.hp1 HG01358.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+3423_63+3424ins others(1): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451893 | |||||||
| chr5:176451893 | T | TATACACA others(120): Show |
1 | a0001c0001t0001g0284 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+3423_63+3424ins others(127): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451893 | |||||||
| chr5:176451894 | T | A | 29 | a0001c0001t0001g0204 a0001c0001t0001g0319 a0001c0001t0002g0004 others(26): Show |
30 | HG01256.hp2 HG01258.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.63+3424T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451894 | |||||||
| chr5:176451895 | T | A | 7 | a0001c0001t0001g0284 a0001c0001t0001g0354 a0001c0001t0002g0288 others(4): Show |
7 | HG02647.hp2 HG02897.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+3425T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451895 | |||||||
| chr5:176451896 | T | A | 24 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0115 others(21): Show |
24 | HG00609.hp2 HG00733.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.63+3426T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451896 | |||||||
| chr5:176451897 | T | A | 26 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0123 others(23): Show |
26 | HG01993.hp2 HG02040.hp2 HG02602.hp2 others(23): Show |
intron_variant | MODIFIER | c.63+3427T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451897 | |||||||
| chr5:176451898 | T | A | 79 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0108 others(76): Show |
79 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.63+3428T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451898 | |||||||
| chr5:176451899 | T | A | 32 | a0001c0001t0001g0116 a0001c0001t0001g0124 a0001c0001t0001g0139 others(29): Show |
34 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.63+3429T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451899 | |||||||
| chr5:176451900 | T | A | 14 | a0001c0001t0001g0108 a0001c0001t0001g0117 a0001c0001t0001g0133 others(11): Show |
14 | HG00438.hp2 HG00621.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+3430T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451900 | |||||||
| chr5:176451901 | T | A | 4 | a0001c0001t0003g0031 a0001c0001t0004g0211 a0001c0001t0004g0218 others(1): Show |
4 | HG02647.hp2 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3431T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451901 | |||||||
| chr5:176451902 | T | A | 6 | a0001c0001t0001g0134 a0001c0001t0001g0146 a0001c0001t0003g0093 others(3): Show |
6 | HG02280.hp1 HG03041.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3432T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451902 | |||||||
| chr5:176451903 | T | A | 2 | a0001c0001t0004g0211 a0001c0001t0013g0020 |
2 | HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.63+3433T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451903 | |||||||
| chr5:176451904 | T | A | 2 | a0001c0001t0001g0134 a0001c0001t0010g0019 |
2 | HG02280.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.63+3434T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451904 | |||||||
| chr5:176451905 | T | A | 1 | a0001c0001t0032g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63+3435T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451905 | |||||||
| chr5:176451962 | C | T | 45 | a0001c0001t0004g0277 a0001c0001t0004g0278 a0001c0001t0004g0279 others(42): Show |
45 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.63+3492C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176451962 | |||||||
| chr5:176452055 | A | G | 3 | a0001c0001t0002g0349 a0001c0001t0002g0351 a0005c0004t0002g0350 |
3 | HG02451.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.63+3585A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176452055 | |||||||
| chr5:176452261 | T | A | 204 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(201): Show |
205 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.63+3791T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176452261 | |||||||
| chr5:176452295 | T | C | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3825T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176452295 | |||||||
| chr5:176452469 | T | G | 301 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(298): Show |
304 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(301): Show |
intron_variant | MODIFIER | c.63+3999T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176452469 | |||||||
| chr5:176452643 | G | C | 3 | a0001c0001t0008g0038 a0001c0001t0008g0039 a0001c0001t0008g0040 |
3 | NA18965.hp2 NA19009.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.63+4173G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176452643 | |||||||
| chr5:176453064 | A | G | 1 | a0001c0001t0005g0282 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.63+4594A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453064 | |||||||
| chr5:176453476 | G | T | 1 | a0001c0001t0001g0354 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.63+5006G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453476 | |||||||
| chr5:176453616 | G | T | 1 | a0001c0001t0001g0354 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.63+5146G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453616 | |||||||
| chr5:176453831 | A | G | 8 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(5): Show |
8 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+5361A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453831 | |||||||
| chr5:176453873 | G | A | 1 | a0001c0001t0006g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+5403G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453873 | |||||||
| chr5:176453988 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.63+5518G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176453988 | |||||||
| chr5:176454013 | A | G | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63+5543A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454013 | |||||||
| chr5:176454042 | A | G | 2 | a0001c0001t0004g0191 a0001c0001t0004g0198 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.63+5572A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454042 | |||||||
| chr5:176454048 | TA | T | 6 | a0001c0001t0001g0109 a0001c0001t0001g0173 a0001c0001t0002g0347 others(3): Show |
6 | HG01081.hp1 HG02132.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+5591delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454048 | ||||||
| chr5:176454190 | C | T | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+5720C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454190 | |||||||
| chr5:176454225 | T | C | 1 | a0001c0001t0005g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.63+5755T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454225 | |||||||
| chr5:176454406 | TAAAAATA others(10): Show |
T | 1 | a0001c0001t0001g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.63+5941_63+5957del others(17): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454406 | ||||||
| chr5:176454533 | G | A | 9 | a0001c0001t0006g0215 a0001c0001t0006g0220 a0001c0001t0006g0221 others(6): Show |
9 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+6063G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454533 | |||||||
| chr5:176454576 | T | C | 4 | a0001c0001t0006g0245 a0001c0001t0006g0246 a0001c0001t0006g0247 others(1): Show |
4 | HG01167.hp1 HG02451.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6106T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454576 | |||||||
| chr5:176454576 | T | G | 2 | a0001c0001t0006g0249 a0001c0001t0006g0250 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.63+6106T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454576 | |||||||
| chr5:176454577 | G | GA | 35 | a0001c0001t0001g0319 a0001c0001t0001g0355 a0001c0001t0002g0287 others(32): Show |
35 | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.63+6141dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | G | GAA | 23 | a0001c0001t0001g0109 a0001c0001t0002g0004 a0001c0001t0002g0289 others(20): Show |
24 | HG00544.hp2 HG00639.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.63+6140_63+6141dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | G | GAAAAAAA others(14): Show |
1 | a0001c0001t0033g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+6121_63+6141dup others(21): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | GA | G | 8 | a0001c0001t0006g0223 a0001c0001t0006g0224 a0001c0001t0006g0225 others(5): Show |
8 | HG01099.hp2 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+6141delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | GAAAAAAA others(2): Show |
G | 9 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(6): Show |
10 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+6133_63+6141del others(9): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | GAAAAAAA others(5): Show |
G | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+6130_63+6141del others(12): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | GAAAAAAA others(6): Show |
G | 10 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0118 others(7): Show |
10 | HG00639.hp2 HG02165.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+6129_63+6141del others(13): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | GAAAAAAA others(7): Show |
G | 131 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(128): Show |
132 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.63+6128_63+6141del others(14): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | GAAAAAAA others(8): Show |
G | 3 | a0001c0001t0001g0190 a0001c0001t0001g0241 a0001c0001t0011g0107 |
3 | HG01256.hp1 HG03490.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.63+6127_63+6141del others(15): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | GAAAAAAA others(9): Show |
G | 4 | a0001c0001t0003g0041 a0001c0001t0003g0042 a0001c0001t0003g0361 others(1): Show |
4 | HG01175.hp2 HG02735.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6126_63+6141del others(16): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | GAAAAAAA others(10): Show |
G | 73 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0002g0096 others(70): Show |
74 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.63+6125_63+6141del others(17): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454577 | GAAAAAAA others(11): Show |
G | 1 | a0001c0001t0005g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.63+6124_63+6141del others(18): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176454577 | ||||||
| chr5:176454634 | A | G | 1 | a0001c0001t0002g0344 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.63+6164A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454634 | |||||||
| chr5:176454661 | A | G | 1 | a0001c0001t0002g0344 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.63+6191A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454661 | |||||||
| chr5:176454673 | A | T | 1 | a0001c0001t0002g0344 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.63+6203A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454673 | |||||||
| chr5:176454695 | T | C | 275 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(272): Show |
277 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.63+6225T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454695 | |||||||
| chr5:176454936 | C | G | 2 | a0001c0001t0010g0005 a0001c0001t0010g0006 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.63+6466C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454936 | |||||||
| chr5:176454945 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.63+6475G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454945 | |||||||
| chr5:176454963 | A | G | 8 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(5): Show |
8 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+6493A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176454963 | |||||||
| chr5:176455075 | T | TA | 9 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(6): Show |
9 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+6616dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176455075 | ||||||
| chr5:176455194 | A | G | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6724A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455194 | |||||||
| chr5:176455221 | G | C | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6751G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455221 | |||||||
| chr5:176455255 | G | A | 42 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(39): Show |
42 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+6785G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455255 | |||||||
| chr5:176455448 | C | CA | 17 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(14): Show |
18 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+6988dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176455448 | ||||||
| chr5:176455508 | G | C | 5 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(2): Show |
6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+7038G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455508 | |||||||
| chr5:176455618 | G | A | 8 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
8 | HG00735.hp1 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+7148G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455618 | |||||||
| chr5:176455708 | T | C | 25 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(22): Show |
26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+7238T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455708 | |||||||
| chr5:176455770 | A | G | 72 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0002g0096 others(69): Show |
73 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.63+7300A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176455770 | |||||||
| chr5:176455853 | C | CTTTATGT others(28): Show |
3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+7391_63+7425dup others(35): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176455853 | ||||||
| chr5:176456084 | T | G | 1 | a0001c0001t0003g0043 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.63+7614T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456084 | |||||||
| chr5:176456137 | T | A | 11 | a0001c0001t0004g0003 a0001c0001t0004g0217 a0001c0001t0004g0218 others(8): Show |
12 | HG01361.hp1 HG01891.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+7667T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456137 | |||||||
| chr5:176456196 | C | G | 1 | a0001c0001t0002g0343 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.63+7726C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456196 | |||||||
| chr5:176456272 | A | T | 4 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+7802A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456272 | |||||||
| chr5:176456516 | A | G | 1 | a0001c0001t0010g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.63+8046A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456516 | |||||||
| chr5:176456576 | C | CCA | 301 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(298): Show |
304 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(301): Show |
intron_variant | MODIFIER | c.63+8107_63+8108ins others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176456576 | ||||||
| chr5:176456877 | G | A | 25 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(22): Show |
26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+8407G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456877 | |||||||
| chr5:176456887 | A | G | 2 | a0001c0001t0003g0032 a0001c0001t0003g0033 |
2 | NA18942.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.63+8417A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176456887 | |||||||
| chr5:176457077 | T | C | 1 | a0001c0001t0004g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.63+8607T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457077 | |||||||
| chr5:176457104 | G | C | 2 | a0001c0001t0007g0366 a0001c0001t0007g0367 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63+8634G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457104 | |||||||
| chr5:176457211 | C | T | 2 | a0001c0001t0007g0366 a0001c0001t0007g0367 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63+8741C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457211 | |||||||
| chr5:176457245 | A | G | 1 | a0001c0001t0005g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.63+8775A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457245 | |||||||
| chr5:176457403 | C | T | 1 | a0001c0001t0018g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.63+8933C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457403 | |||||||
| chr5:176457486 | C | T | 71 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(68): Show |
72 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.63+9016C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457486 | |||||||
| chr5:176457596 | T | C | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+9126T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457596 | |||||||
| chr5:176457653 | G | GGT | 65 | a0001c0001t0002g0096 a0001c0001t0004g0208 a0001c0001t0004g0277 others(62): Show |
65 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.63+9204_63+9205dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176457653 | ||||||
| chr5:176457653 | G | GGTGT | 140 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0108 others(137): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.63+9202_63+9205dup others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176457653 | ||||||
| chr5:176457653 | G | GGTGTGT | 5 | a0001c0001t0001g0104 a0001c0001t0001g0159 a0001c0001t0001g0174 others(2): Show |
5 | HG00639.hp2 HG02080.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+9200_63+9205dup others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176457653 | ||||||
| chr5:176457655 | T | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | NA18975.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.63+9185T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457655 | |||||||
| chr5:176457662 | G | T | 10 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(7): Show |
10 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+9192G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457662 | |||||||
| chr5:176457714 | T | C | 1 | a0001c0001t0003g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.63+9244T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457714 | |||||||
| chr5:176457774 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01975.hp1 HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.63+9304A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457774 | |||||||
| chr5:176457844 | T | C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0154 a0001c0001t0001g0173 others(1): Show |
4 | HG02165.hp2 NA18941.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+9374T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457844 | |||||||
| chr5:176457902 | G | A | 4 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+9432G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176457902 | |||||||
| chr5:176458006 | A | G | 10 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(7): Show |
10 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+9536A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458006 | |||||||
| chr5:176458079 | CCTCTTCT others(5): Show |
C | 10 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(7): Show |
10 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+9618_63+9629del others(12): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458079 | ||||||
| chr5:176458109 | A | G | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+9639A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458109 | |||||||
| chr5:176458197 | T | C | 4 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+9727T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458197 | |||||||
| chr5:176458228 | C | T | 1 | a0001c0001t0006g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+9758C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458228 | |||||||
| chr5:176458407 | C | T | 25 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(22): Show |
26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+9937C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458407 | |||||||
| chr5:176458408 | C | CTTTTT | 8 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0001t0001g0146 others(5): Show |
8 | HG01070.hp2 HG02897.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+9953_63+9957dup others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458408 | ||||||
| chr5:176458408 | C | CTTTTTTT | 102 | a0001c0001t0001g0117 a0001c0001t0001g0147 a0001c0001t0001g0148 others(99): Show |
104 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.63+9951_63+9957dup others(7): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458408 | ||||||
| chr5:176458408 | C | CTTTTTTT others(1): Show |
22 | a0001c0001t0001g0319 a0001c0001t0002g0096 a0001c0001t0002g0303 others(19): Show |
22 | HG00733.hp1 HG01099.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.63+9950_63+9957dup others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458408 | ||||||
| chr5:176458408 | CT | C | 6 | a0001c0001t0005g0267 a0001c0001t0007g0366 a0001c0001t0007g0367 others(3): Show |
6 | HG02280.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9957delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458408 | ||||||
| chr5:176458433 | G | A | 2 | a0001c0001t0007g0366 a0001c0001t0007g0367 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63+9963G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458433 | |||||||
| chr5:176458436 | GTCTCACT others(1): Show |
G | 20 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(17): Show |
21 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.63+9973_63+9980del others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176458436 | ||||||
| chr5:176458455 | G | A | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+9985G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458455 | |||||||
| chr5:176458473 | G | A | 1 | a0001c0001t0024g0236 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+10003G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458473 | |||||||
| chr5:176458639 | C | T | 143 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(140): Show |
144 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.63+10169C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458639 | |||||||
| chr5:176458824 | C | A | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+10354C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176458824 | |||||||
| chr5:176459143 | G | GT | 5 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(2): Show |
6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10679dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176459143 | ||||||
| chr5:176459219 | A | G | 4 | a0001c0001t0006g0270 a0001c0001t0006g0271 a0001c0001t0006g0272 others(1): Show |
4 | HG01496.hp2 NA18906.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+10749A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459219 | |||||||
| chr5:176459250 | C | CT | 93 | a0001c0001t0001g0113 a0001c0001t0001g0135 a0001c0001t0001g0170 others(90): Show |
94 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.63+10800dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176459250 | ||||||
| chr5:176459250 | C | CTT | 63 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(60): Show |
64 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.63+10799_63+10800d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176459250 | ||||||
| chr5:176459250 | C | CTTT | 8 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0041 others(5): Show |
8 | HG02132.hp2 HG04184.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+10798_63+10800d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176459250 | ||||||
| chr5:176459250 | CT | C | 31 | a0001c0001t0001g0106 a0001c0001t0001g0116 a0001c0001t0001g0134 others(28): Show |
32 | HG00438.hp2 HG00733.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+10800delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176459250 | ||||||
| chr5:176459297 | T | C | 25 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(22): Show |
26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+10827T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459297 | |||||||
| chr5:176459413 | C | T | 1 | a0001c0001t0003g0069 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.63+10943C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459413 | |||||||
| chr5:176459503 | G | A | 1 | a0001c0001t0002g0349 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+11033G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459503 | |||||||
| chr5:176459546 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.63+11076G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459546 | |||||||
| chr5:176459685 | A | G | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | NA18951.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.63+11215A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459685 | |||||||
| chr5:176459706 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.63+11236T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459706 | |||||||
| chr5:176459747 | A | G | 1 | a0001c0001t0013g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.63+11277A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176459747 | |||||||
| chr5:176460055 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.63+11585A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460055 | |||||||
| chr5:176460153 | T | C | 1 | a0001c0001t0002g0347 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.63+11683T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460153 | |||||||
| chr5:176460155 | C | T | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+11685C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460155 | |||||||
| chr5:176460250 | A | T | 1 | a0001c0001t0002g0302 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.63+11780A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460250 | |||||||
| chr5:176460263 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.63+11793G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460263 | |||||||
| chr5:176460278 | C | G | 3 | a0001c0001t0010g0019 a0001c0001t0010g0021 a0001c0001t0013g0020 |
3 | HG02280.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.63+11808C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460278 | |||||||
| chr5:176460502 | A | G | 3 | a0001c0001t0010g0019 a0001c0001t0010g0021 a0001c0001t0013g0020 |
3 | HG02280.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.63+12032A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460502 | |||||||
| chr5:176460513 | C | CGT | 158 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0109 others(155): Show |
159 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.63+12082_63+12083d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460513 | C | CGTGT | 47 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0134 others(44): Show |
47 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+12080_63+12083d others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460513 | C | CGTGTGT | 21 | a0001c0001t0001g0106 a0001c0001t0001g0145 a0001c0001t0003g0063 others(18): Show |
21 | HG00733.hp2 HG01099.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.63+12078_63+12083d others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460513 | C | CGTGTGTG others(1): Show |
16 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0003g0065 others(13): Show |
16 | HG00544.hp2 HG02074.hp2 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+12076_63+12083d others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460513 | C | CGTGTGTG others(7): Show |
1 | a0001c0001t0010g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+12070_63+12083d others(16): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460513 | C | T | 1 | a0001c0001t0004g0233 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+12043C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460513 | |||||||
| chr5:176460513 | CGT | C | 29 | a0001c0001t0001g0213 a0001c0001t0002g0323 a0001c0001t0002g0348 others(26): Show |
30 | HG00280.hp2 HG00733.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.63+12082_63+12083d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460513 | CGTGT | C | 10 | a0001c0001t0001g0284 a0001c0001t0003g0074 a0001c0001t0004g0022 others(7): Show |
10 | HG01433.hp2 HG02080.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+12080_63+12083d others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460513 | CGTGTGT | C | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+12078_63+12083d others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460513 | CGTGTGTG others(3): Show |
C | 4 | a0001c0001t0002g0349 a0001c0001t0002g0351 a0001c0001t0003g0045 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+12074_63+12083d others(12): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460513 | CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0001g0177 a0001c0001t0002g0339 |
2 | HG00423.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.63+12072_63+12083d others(14): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460513 | CGTGTGTG others(13): Show |
C | 5 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(2): Show |
6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+12064_63+12083d others(22): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176460513 | ||||||
| chr5:176460554 | A | T | 1 | a0001c0001t0001g0189 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.63+12084A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460554 | |||||||
| chr5:176460595 | G | A | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+12125G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460595 | |||||||
| chr5:176460614 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+12144C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460614 | |||||||
| chr5:176460675 | G | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+12205G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460675 | |||||||
| chr5:176460685 | C | G | 2 | a0001c0001t0001g0319 a0001c0001t0002g0344 |
2 | HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.63+12215C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460685 | |||||||
| chr5:176460689 | C | T | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+12219C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460689 | |||||||
| chr5:176460781 | A | G | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63+12311A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460781 | |||||||
| chr5:176460823 | A | G | 25 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(22): Show |
26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+12353A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176460823 | |||||||
| chr5:176461014 | T | G | 5 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(2): Show |
6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+12544T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461014 | |||||||
| chr5:176461018 | CT | C | 299 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(296): Show |
302 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.63+12560delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461018 | ||||||
| chr5:176461097 | C | T | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+12627C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461097 | |||||||
| chr5:176461163 | A | G | 3 | a0001c0001t0003g0044 a0001c0001t0003g0068 a0001c0001t0003g0069 |
3 | NA18983.hp1 NA18984.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.63+12693A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461163 | |||||||
| chr5:176461234 | G | A | 1 | a0001c0001t0013g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.63+12764G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461234 | |||||||
| chr5:176461312 | C | CT | 200 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0108 others(197): Show |
202 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.63+12866dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461312 | ||||||
| chr5:176461312 | C | CTT | 111 | a0001c0001t0001g0035 a0001c0001t0001g0095 a0001c0001t0001g0113 others(108): Show |
113 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.63+12865_63+12866d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461312 | ||||||
| chr5:176461312 | C | CTTT | 8 | a0001c0001t0001g0036 a0001c0001t0002g0351 a0001c0001t0003g0064 others(5): Show |
8 | HG02615.hp1 HG02922.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+12864_63+12866d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461312 | ||||||
| chr5:176461484 | A | AT | 11 | a0001c0001t0002g0309 a0001c0001t0002g0311 a0001c0001t0002g0312 others(8): Show |
11 | HG00280.hp1 HG01081.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+13022dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461484 | ||||||
| chr5:176461498 | A | T | 8 | a0001c0001t0006g0245 a0001c0001t0006g0249 a0001c0001t0006g0250 others(5): Show |
8 | HG01496.hp2 HG03139.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+13028A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461498 | |||||||
| chr5:176461502 | T | A | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+13032T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461502 | |||||||
| chr5:176461503 | T | A | 140 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(137): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.63+13033T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461503 | |||||||
| chr5:176461622 | C | T | 1 | a0001c0001t0004g0279 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.63+13152C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461622 | |||||||
| chr5:176461626 | C | A | 1 | a0001c0001t0003g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.63+13156C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461626 | |||||||
| chr5:176461651 | G | GTTA | 7 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(4): Show |
8 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+13196_63+13198d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461651 | ||||||
| chr5:176461768 | T | C | 1 | a0001c0001t0002g0347 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.63+13298T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461768 | |||||||
| chr5:176461814 | CT | C | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+13347delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176461814 | ||||||
| chr5:176461938 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.63+13468C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461938 | |||||||
| chr5:176461972 | G | C | 1 | a0001c0001t0002g0316 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.63+13502G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176461972 | |||||||
| chr5:176462015 | A | G | 300 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(297): Show |
303 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(300): Show |
intron_variant | MODIFIER | c.63+13545A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462015 | |||||||
| chr5:176462091 | A | G | 16 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0037 others(13): Show |
16 | HG00558.hp2 HG01081.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+13621A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462091 | |||||||
| chr5:176462201 | A | G | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.63+13731A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462201 | |||||||
| chr5:176462256 | G | A | 300 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(297): Show |
303 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(300): Show |
intron_variant | MODIFIER | c.63+13786G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462256 | |||||||
| chr5:176462315 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.63+13845A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462315 | |||||||
| chr5:176462425 | A | T | 1 | a0001c0001t0002g0303 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.63+13955A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462425 | |||||||
| chr5:176462432 | T | TG | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+13964dupG | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176462432 | ||||||
| chr5:176462451 | C | T | 1 | a0001c0001t0002g0315 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+13981C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462451 | |||||||
| chr5:176462480 | C | T | 205 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(202): Show |
206 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.63+14010C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462480 | |||||||
| chr5:176462601 | C | T | 5 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(2): Show |
5 | HG02486.hp1 NA18955.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+14131C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462601 | |||||||
| chr5:176462916 | G | A | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+14446G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462916 | |||||||
| chr5:176462969 | A | G | 1 | a0001c0001t0004g0120 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+14499A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462969 | |||||||
| chr5:176462974 | G | A | 143 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(140): Show |
144 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.63+14504G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176462974 | |||||||
| chr5:176463041 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.63+14571G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463041 | |||||||
| chr5:176463384 | C | CA | 9 | a0001c0001t0003g0064 a0001c0001t0004g0007 a0001c0001t0004g0008 others(6): Show |
9 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+14926dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176463384 | ||||||
| chr5:176463425 | T | C | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+14955T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463425 | |||||||
| chr5:176463724 | G | GT | 24 | a0001c0001t0001g0145 a0001c0001t0001g0174 a0001c0001t0001g0200 others(21): Show |
24 | HG00408.hp2 HG00621.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.63+15273dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176463724 | ||||||
| chr5:176463724 | GT | G | 25 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(22): Show |
26 | HG00558.hp2 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+15273delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176463724 | ||||||
| chr5:176463730 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.63+15260T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463730 | |||||||
| chr5:176463731 | T | G | 1 | a0001c0001t0019g0326 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.63+15261T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463731 | |||||||
| chr5:176463766 | G | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+15296G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463766 | |||||||
| chr5:176463847 | A | G | 70 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(67): Show |
71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-15341A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463847 | |||||||
| chr5:176463889 | C | T | 21 | a0001c0001t0005g0027 a0001c0001t0005g0103 a0001c0001t0005g0251 others(18): Show |
21 | HG00544.hp2 HG02015.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-15299C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463889 | |||||||
| chr5:176463918 | C | T | 1 | a0001c0001t0010g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64-15270C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463918 | |||||||
| chr5:176463966 | G | A | 1 | a0001c0001t0005g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.64-15222G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463966 | |||||||
| chr5:176463996 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64-15192C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176463996 | |||||||
| chr5:176464017 | A | G | 3 | a0001c0001t0002g0309 a0001c0001t0002g0311 a0001c0001t0002g0347 |
3 | HG00280.hp1 HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.64-15171A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464017 | |||||||
| chr5:176464025 | G | A | 12 | a0001c0001t0004g0120 a0001c0001t0004g0149 a0001c0001t0004g0169 others(9): Show |
12 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-15163G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464025 | |||||||
| chr5:176464027 | G | C | 1 | a0001c0001t0010g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64-15161G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464027 | |||||||
| chr5:176464051 | A | G | 25 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(22): Show |
26 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.64-15137A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464051 | |||||||
| chr5:176464098 | C | T | 9 | a0001c0001t0006g0215 a0001c0001t0006g0220 a0001c0001t0006g0221 others(6): Show |
9 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-15090C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464098 | |||||||
| chr5:176464284 | G | C | 1 | a0001c0001t0008g0040 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.64-14904G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464284 | |||||||
| chr5:176464487 | CT | C | 64 | a0001c0001t0001g0319 a0001c0001t0001g0345 a0001c0001t0001g0355 others(61): Show |
65 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.64-14678delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176464487 | ||||||
| chr5:176464487 | CTT | C | 13 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0183 others(10): Show |
13 | HG00621.hp1 HG01361.hp2 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-14679_64-14678d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176464487 | ||||||
| chr5:176464487 | CTTT | C | 278 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(275): Show |
281 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(278): Show |
intron_variant | MODIFIER | c.64-14680_64-14678d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176464487 | ||||||
| chr5:176464525 | C | T | 1 | a0001c0001t0004g0219 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64-14663C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176464525 | |||||||
| chr5:176465107 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.64-14081T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465107 | |||||||
| chr5:176465221 | C | T | 1 | a0001c0001t0004g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.64-13967C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465221 | |||||||
| chr5:176465366 | C | CT | 11 | a0001c0001t0001g0148 a0001c0001t0002g0301 a0001c0001t0002g0342 others(8): Show |
11 | HG01928.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-13804dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176465366 | ||||||
| chr5:176465366 | CT | C | 249 | a0001c0001t0001g0035 a0001c0001t0001g0095 a0001c0001t0001g0104 others(246): Show |
251 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.64-13804delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176465366 | ||||||
| chr5:176465367 | T | TTTC | 5 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(2): Show |
6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-13819_64-13818i others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176465367 | ||||||
| chr5:176465370 | T | C | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-13818T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465370 | |||||||
| chr5:176465414 | C | T | 70 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(67): Show |
71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-13774C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465414 | |||||||
| chr5:176465648 | T | A | 3 | a0001c0001t0002g0349 a0001c0001t0002g0351 a0005c0004t0002g0350 |
3 | HG02451.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.64-13540T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465648 | |||||||
| chr5:176465873 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.64-13315C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465873 | |||||||
| chr5:176465980 | T | G | 1 | a0001c0001t0004g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-13208T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176465980 | |||||||
| chr5:176466030 | T | C | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG00733.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-13158T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466030 | |||||||
| chr5:176466062 | G | A | 298 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(295): Show |
301 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.64-13126G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466062 | |||||||
| chr5:176466119 | A | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-13069A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466119 | |||||||
| chr5:176466126 | G | C | 2 | a0001c0001t0004g0191 a0001c0001t0004g0198 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64-13062G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466126 | |||||||
| chr5:176466190 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.64-12998C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466190 | |||||||
| chr5:176466212 | C | T | 5 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(2): Show |
6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-12976C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466212 | |||||||
| chr5:176466460 | C | T | 2 | a0001c0001t0010g0005 a0001c0001t0010g0006 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64-12728C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466460 | |||||||
| chr5:176466575 | T | G | 273 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(270): Show |
275 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.64-12613T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466575 | |||||||
| chr5:176466651 | C | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-12537C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466651 | |||||||
| chr5:176466658 | A | C | 1 | a0001c0001t0009g0097 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64-12530A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466658 | |||||||
| chr5:176466813 | G | GTAGGAAA others(30): Show |
8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-12374_64-12338d others(39): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176466813 | ||||||
| chr5:176466941 | C | A | 142 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(139): Show |
143 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.64-12247C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466941 | |||||||
| chr5:176466948 | G | A | 2 | a0001c0001t0007g0366 a0001c0001t0007g0367 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.64-12240G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176466948 | |||||||
| chr5:176467038 | G | C | 70 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(67): Show |
71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-12150G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467038 | |||||||
| chr5:176467118 | T | C | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-12070T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467118 | |||||||
| chr5:176467127 | T | C | 1 | a0001c0001t0004g0239 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.64-12061T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467127 | |||||||
| chr5:176467128 | C | T | 1 | a0001c0001t0005g0254 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.64-12060C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467128 | |||||||
| chr5:176467129 | CT | C | 112 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0002g0004 others(109): Show |
113 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.64-12035delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467129 | ||||||
| chr5:176467129 | CTT | C | 36 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(33): Show |
37 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.64-12036_64-12035d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467129 | ||||||
| chr5:176467129 | CTTT | C | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-12037_64-12035d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467129 | ||||||
| chr5:176467129 | CTTTTTTT | C | 111 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0108 others(108): Show |
111 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.64-12041_64-12035d others(9): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467129 | ||||||
| chr5:176467131 | T | C | 1 | a0001c0001t0005g0254 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.64-12057T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467131 | |||||||
| chr5:176467135 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64-12053T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467135 | |||||||
| chr5:176467136 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64-12052T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467136 | |||||||
| chr5:176467330 | G | GT | 6 | a0001c0001t0002g0337 a0001c0001t0003g0034 a0001c0001t0003g0045 others(3): Show |
6 | HG01109.hp1 HG02056.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-11850dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467330 | ||||||
| chr5:176467330 | G | T | 6 | a0001c0001t0004g0238 a0001c0001t0007g0366 a0001c0001t0007g0367 others(3): Show |
6 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-11858G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467330 | |||||||
| chr5:176467339 | G | T | 2 | a0001c0001t0007g0366 a0001c0001t0007g0367 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.64-11849G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467339 | |||||||
| chr5:176467340 | G | T | 1 | a0001c0001t0008g0039 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.64-11848G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467340 | |||||||
| chr5:176467454 | C | T | 3 | a0001c0001t0011g0107 a0001c0001t0011g0137 a0001c0001t0011g0138 |
3 | NA18969.hp1 NA19060.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.64-11734C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467454 | |||||||
| chr5:176467499 | C | T | 1 | a0001c0001t0017g0276 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.64-11689C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467499 | |||||||
| chr5:176467585 | G | A | 4 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0064 others(1): Show |
4 | NA18977.hp2 NA19056.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-11603G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467585 | |||||||
| chr5:176467632 | A | G | 1 | a0005c0004t0002g0350 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.64-11556A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467632 | |||||||
| chr5:176467734 | T | G | 5 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(2): Show |
6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-11454T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467734 | |||||||
| chr5:176467778 | T | C | 5 | a0001c0001t0004g0277 a0001c0001t0004g0278 a0001c0001t0004g0279 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-11410T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467778 | |||||||
| chr5:176467806 | AT | A | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-11380delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176467806 | ||||||
| chr5:176467810 | G | T | 2 | a0001c0001t0004g0238 a0001c0001t0004g0353 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-11378G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467810 | |||||||
| chr5:176467861 | A | C | 1 | a0001c0001t0002g0315 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.64-11327A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467861 | |||||||
| chr5:176467925 | G | T | 1 | a0001c0001t0001g0345 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.64-11263G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176467925 | |||||||
| chr5:176468022 | G | A | 273 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(270): Show |
275 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.64-11166G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468022 | |||||||
| chr5:176468096 | C | T | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64-11092C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468096 | |||||||
| chr5:176468109 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64-11079G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468109 | |||||||
| chr5:176468244 | C | A | 1 | a0001c0001t0009g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-10944C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468244 | |||||||
| chr5:176468317 | G | A | 1 | a0001c0001t0004g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.64-10871G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468317 | |||||||
| chr5:176468403 | T | C | 1 | a0001c0001t0004g0279 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64-10785T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468403 | |||||||
| chr5:176468412 | G | A | 10 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(7): Show |
11 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-10776G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468412 | |||||||
| chr5:176468520 | C | G | 70 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(67): Show |
71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-10668C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468520 | |||||||
| chr5:176468785 | C | CA | 9 | a0001c0001t0004g0105 a0001c0001t0004g0217 a0001c0001t0006g0224 others(6): Show |
9 | HG01515.hp2 HG01517.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-10391dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176468785 | ||||||
| chr5:176468785 | CA | C | 16 | a0001c0001t0003g0064 a0001c0001t0004g0007 a0001c0001t0004g0008 others(13): Show |
17 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-10391delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176468785 | ||||||
| chr5:176468815 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-10373G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468815 | |||||||
| chr5:176468849 | C | T | 3 | a0001c0001t0010g0019 a0001c0001t0010g0021 a0001c0001t0013g0020 |
3 | HG02280.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.64-10339C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176468849 | |||||||
| chr5:176469232 | G | A | 1 | a0001c0001t0003g0079 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-9956G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469232 | |||||||
| chr5:176469482 | C | T | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-9706C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469482 | |||||||
| chr5:176469645 | A | G | 8 | a0001c0001t0001g0122 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG01934.hp1 HG01952.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-9543A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469645 | |||||||
| chr5:176469760 | C | T | 1 | a0001c0001t0013g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64-9428C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469760 | |||||||
| chr5:176469773 | T | G | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-9415T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469773 | |||||||
| chr5:176469861 | G | A | 1 | a0001c0001t0003g0046 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64-9327G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176469861 | |||||||
| chr5:176470219 | C | G | 142 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(139): Show |
143 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.64-8969C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470219 | |||||||
| chr5:176470310 | A | G | 299 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(296): Show |
302 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.64-8878A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470310 | |||||||
| chr5:176470368 | G | A | 1 | a0006c0007t0002g0330 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.64-8820G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470368 | |||||||
| chr5:176470420 | A | G | 4 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-8768A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470420 | |||||||
| chr5:176470437 | C | T | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-8751C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470437 | |||||||
| chr5:176470460 | C | A | 1 | a0001c0001t0004g0278 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.64-8728C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470460 | |||||||
| chr5:176470475 | G | T | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-8713G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470475 | |||||||
| chr5:176470532 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.64-8656G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470532 | |||||||
| chr5:176470541 | C | T | 71 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0125 others(68): Show |
72 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.64-8647C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470541 | |||||||
| chr5:176470637 | TCACA | T | 10 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(7): Show |
11 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-8542_64-8539del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176470637 | ||||||
| chr5:176470648 | C | A | 1 | a0001c0001t0009g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-8540C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176470648 | |||||||
| chr5:176471197 | G | A | 1 | a0001c0001t0005g0269 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.64-7991G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471197 | |||||||
| chr5:176471303 | T | G | 7 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(4): Show |
8 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-7885T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471303 | |||||||
| chr5:176471309 | A | G | 2 | a0001c0001t0010g0005 a0001c0001t0010g0006 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64-7879A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471309 | |||||||
| chr5:176471331 | A | G | 1 | a0001c0001t0007g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.64-7857A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471331 | |||||||
| chr5:176471375 | C | CT | 9 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0293 others(6): Show |
9 | HG01256.hp2 HG01258.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-7789dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | ||||||
| chr5:176471375 | CTT | C | 6 | a0001c0001t0001g0035 a0001c0001t0003g0041 a0001c0001t0003g0063 others(3): Show |
6 | HG01070.hp1 HG02145.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-7790_64-7789del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | ||||||
| chr5:176471375 | CTTT | C | 78 | a0001c0001t0001g0036 a0001c0001t0001g0125 a0001c0001t0003g0002 others(75): Show |
79 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.64-7791_64-7789del others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | ||||||
| chr5:176471375 | CTTTT | C | 16 | a0001c0001t0001g0110 a0001c0001t0001g0174 a0001c0001t0001g0182 others(13): Show |
16 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-7792_64-7789del others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | ||||||
| chr5:176471375 | CTTTTT | C | 186 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(183): Show |
187 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.64-7793_64-7789del others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | ||||||
| chr5:176471375 | CTTTTTT | C | 8 | a0001c0001t0001g0109 a0001c0001t0001g0358 a0001c0001t0004g0184 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-7794_64-7789del others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471375 | ||||||
| chr5:176471432 | G | C | 1 | a0001c0001t0013g0026 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64-7756G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471432 | |||||||
| chr5:176471679 | G | A | 1 | a0001c0001t0003g0079 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-7509G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471679 | |||||||
| chr5:176471684 | CT | C | 255 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(252): Show |
258 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.64-7488delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176471684 | ||||||
| chr5:176471704 | A | T | 1 | a0001c0001t0004g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-7484A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471704 | |||||||
| chr5:176471711 | C | A | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG01975.hp1 HG01993.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-7477C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471711 | |||||||
| chr5:176471880 | G | A | 70 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(67): Show |
71 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-7308G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471880 | |||||||
| chr5:176471973 | C | T | 2 | a0001c0001t0010g0005 a0001c0001t0010g0006 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64-7215C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471973 | |||||||
| chr5:176471981 | C | G | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64-7207C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471981 | |||||||
| chr5:176471996 | C | A | 298 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(295): Show |
301 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.64-7192C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176471996 | |||||||
| chr5:176472135 | T | A | 1 | a0001c0001t0002g0306 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64-7053T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472135 | |||||||
| chr5:176472147 | T | G | 1 | a0001c0001t0006g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-7041T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472147 | |||||||
| chr5:176472277 | G | T | 5 | a0001c0001t0008g0038 a0001c0001t0008g0039 a0001c0001t0008g0040 others(2): Show |
5 | NA18947.hp2 NA18965.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6911G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472277 | |||||||
| chr5:176472452 | G | GT | 5 | a0001c0001t0007g0366 a0001c0001t0007g0367 a0001c0001t0010g0019 others(2): Show |
5 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6728dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176472452 | ||||||
| chr5:176472461 | A | G | 1 | a0001c0001t0003g0057 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.64-6727A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472461 | |||||||
| chr5:176472719 | CA | C | 18 | a0001c0001t0001g0174 a0001c0001t0002g0349 a0001c0001t0002g0351 others(15): Show |
18 | HG02451.hp1 HG02615.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-6453delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176472719 | ||||||
| chr5:176472719 | CAA | C | 284 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(281): Show |
287 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(284): Show |
intron_variant | MODIFIER | c.64-6454_64-6453del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176472719 | ||||||
| chr5:176472735 | A | G | 1 | a0001c0001t0003g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.64-6453A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472735 | |||||||
| chr5:176472810 | A | G | 1 | a0001c0001t0005g0253 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.64-6378A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176472810 | |||||||
| chr5:176473114 | T | A | 298 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(295): Show |
301 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.64-6074T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473114 | |||||||
| chr5:176473179 | G | A | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-6009G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473179 | |||||||
| chr5:176473503 | C | T | 4 | a0001c0001t0003g0043 a0001c0001t0003g0048 a0001c0001t0003g0050 others(1): Show |
4 | HG00621.hp1 HG02071.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-5685C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473503 | |||||||
| chr5:176473527 | A | G | 20 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(17): Show |
21 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-5661A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473527 | |||||||
| chr5:176473728 | C | T | 4 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-5460C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473728 | |||||||
| chr5:176473729 | G | A | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-5459G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473729 | |||||||
| chr5:176473914 | T | G | 3 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 |
3 | NA18971.hp2 NA19054.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.64-5274T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473914 | |||||||
| chr5:176473955 | G | A | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64-5233G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176473955 | |||||||
| chr5:176474070 | C | T | 4 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
5 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-5118C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474070 | |||||||
| chr5:176474208 | T | C | 2 | a0001c0001t0007g0366 a0001c0001t0007g0367 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.64-4980T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474208 | |||||||
| chr5:176474317 | C | T | 1 | a0001c0001t0004g0003 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.64-4871C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474317 | |||||||
| chr5:176474391 | A | T | 138 | a0001c0001t0001g0109 a0001c0001t0001g0118 a0001c0001t0001g0123 others(135): Show |
141 | HG00408.hp1 HG00558.hp2 HG00642.hp2 others(138): Show |
intron_variant | MODIFIER | c.64-4797A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474391 | |||||||
| chr5:176474419 | T | C | 2 | a0001c0001t0004g0023 a0001c0001t0004g0024 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64-4769T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474419 | |||||||
| chr5:176474446 | AC | A | 24 | a0001c0001t0004g0105 a0001c0001t0004g0209 a0001c0001t0004g0210 others(21): Show |
25 | HG00280.hp2 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.64-4736delC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176474446 | ||||||
| chr5:176474457 | C | T | 1 | a0001c0001t0004g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-4731C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474457 | |||||||
| chr5:176474584 | T | C | 10 | a0001c0001t0004g0003 a0001c0001t0004g0217 a0001c0001t0004g0218 others(7): Show |
11 | HG01361.hp1 HG01891.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-4604T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474584 | |||||||
| chr5:176474619 | A | G | 2 | a0001c0001t0002g0292 a0001c0001t0002g0293 |
2 | NA18945.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.64-4569A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176474619 | |||||||
| chr5:176475101 | G | C | 2 | a0001c0001t0004g0191 a0001c0001t0004g0198 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64-4087G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475101 | |||||||
| chr5:176475137 | G | GTTA | 76 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0205 others(73): Show |
77 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.64-4036_64-4034dup others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176475137 | ||||||
| chr5:176475195 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-3993C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475195 | |||||||
| chr5:176475339 | G | C | 1 | a0001c0001t0002g0312 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.64-3849G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475339 | |||||||
| chr5:176475480 | T | C | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | NA19056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.64-3708T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475480 | |||||||
| chr5:176475596 | C | T | 1 | a0001c0001t0002g0290 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.64-3592C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475596 | |||||||
| chr5:176475611 | T | C | 2 | a0001c0001t0004g0209 a0001c0001t0004g0210 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.64-3577T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475611 | |||||||
| chr5:176475699 | C | T | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3489C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475699 | |||||||
| chr5:176475880 | A | G | 1 | a0001c0001t0002g0315 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.64-3308A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475880 | |||||||
| chr5:176475924 | A | G | 1 | a0002c0002t0001g0166 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.64-3264A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475924 | |||||||
| chr5:176475951 | A | G | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-3237A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176475951 | |||||||
| chr5:176476124 | G | T | 2 | a0001c0001t0003g0075 a0001c0001t0003g0076 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.64-3064G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476124 | |||||||
| chr5:176476129 | G | A | 1 | a0001c0001t0001g0284 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.64-3059G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476129 | |||||||
| chr5:176476262 | T | C | 2 | a0001c0001t0003g0041 a0001c0001t0003g0054 |
2 | HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.64-2926T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476262 | |||||||
| chr5:176476359 | G | A | 1 | a0001c0001t0002g0344 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.64-2829G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476359 | |||||||
| chr5:176476471 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0188 |
2 | NA18945.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.64-2717G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476471 | |||||||
| chr5:176476627 | C | CT | 64 | a0001c0001t0001g0095 a0001c0001t0001g0112 a0001c0001t0001g0121 others(61): Show |
65 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.64-2538dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | ||||||
| chr5:176476627 | C | CTT | 12 | a0001c0001t0005g0251 a0001c0001t0005g0258 a0001c0001t0005g0260 others(9): Show |
12 | HG00438.hp1 HG01167.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-2539_64-2538dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | ||||||
| chr5:176476627 | CT | C | 9 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0173 others(6): Show |
9 | HG01175.hp1 HG02922.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-2538delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | ||||||
| chr5:176476627 | CTT | C | 7 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0007g0366 others(4): Show |
7 | HG02280.hp1 HG02809.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-2539_64-2538del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | ||||||
| chr5:176476627 | CTTT | C | 66 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(63): Show |
67 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-2540_64-2538del others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | ||||||
| chr5:176476627 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0031g0119 |
3 | HG02602.hp2 HG02683.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.64-2547_64-2538del others(10): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476627 | ||||||
| chr5:176476673 | C | T | 27 | a0001c0001t0005g0027 a0001c0001t0005g0244 a0001c0001t0005g0251 others(24): Show |
27 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.64-2515C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176476673 | |||||||
| chr5:176476804 | A | AT | 69 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0112 others(66): Show |
69 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.64-2361dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476804 | ||||||
| chr5:176476804 | A | ATT | 11 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0023 others(8): Show |
12 | HG00280.hp2 HG01069.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-2362_64-2361dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476804 | ||||||
| chr5:176476804 | AT | A | 7 | a0001c0001t0001g0180 a0001c0001t0001g0319 a0001c0001t0002g0309 others(4): Show |
7 | HG00280.hp1 HG01169.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-2361delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176476804 | ||||||
| chr5:176477029 | C | T | 1 | a0006c0007t0002g0330 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.64-2159C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477029 | |||||||
| chr5:176477043 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0231 |
2 | NA19009.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.64-2145C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477043 | |||||||
| chr5:176477070 | A | G | 147 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(144): Show |
148 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.64-2118A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477070 | |||||||
| chr5:176477087 | C | T | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-2101C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477087 | |||||||
| chr5:176477088 | GTGAGCCA others(130): Show |
G | 1 | a0001c0001t0002g0336 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.64-2062_64-1926del | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477088 | ||||||
| chr5:176477098 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.64-2090G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477098 | |||||||
| chr5:176477099 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.64-2089T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477099 | |||||||
| chr5:176477100 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.64-2088G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477100 | |||||||
| chr5:176477106 | CCT | C | 3 | a0001c0001t0013g0026 a0001c0001t0014g0014 a0001c0001t0014g0015 |
3 | HG01891.hp2 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-2081_64-2080del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477106 | |||||||
| chr5:176477106 | CCTT | C | 17 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(14): Show |
18 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-2081_64-2079del others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477106 | |||||||
| chr5:176477107 | C | CT | 33 | a0001c0001t0001g0128 a0001c0001t0001g0159 a0001c0001t0001g0165 others(30): Show |
33 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.64-2063dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477107 | ||||||
| chr5:176477107 | CTTTTTTT others(131): Show |
C | 2 | a0001c0001t0002g0323 a0001c0001t0002g0340 |
2 | NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.64-2062_64-1925del | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477107 | ||||||
| chr5:176477107 | CTTTTTTT others(132): Show |
C | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.64-2058_64-1920del | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477107 | ||||||
| chr5:176477136 | G | A | 1 | a0001c0001t0002g0302 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.64-2052G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477136 | |||||||
| chr5:176477140 | T | C | 138 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(135): Show |
138 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.64-2048T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477140 | |||||||
| chr5:176477172 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0178 |
2 | NA19072.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.64-2016C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477172 | |||||||
| chr5:176477187 | T | C | 1 | a0001c0001t0005g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-2001T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477187 | |||||||
| chr5:176477225 | A | G | 2 | a0001c0001t0004g0278 a0001c0001t0032g0098 |
2 | HG02080.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.64-1963A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477225 | |||||||
| chr5:176477235 | G | A | 2 | a0001c0001t0007g0366 a0001c0001t0007g0367 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.64-1953G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477235 | |||||||
| chr5:176477236 | T | C | 2 | a0001c0001t0007g0366 a0001c0001t0007g0367 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.64-1952T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477236 | |||||||
| chr5:176477243 | C | CTTTTTTT others(126): Show |
1 | a0001c0001t0032g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64-1945_64-1944ins others(133): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477243 | |||||||
| chr5:176477244 | CT | C | 178 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(175): Show |
178 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.64-1924delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477244 | ||||||
| chr5:176477244 | CTT | C | 80 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0116 others(77): Show |
81 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.64-1925_64-1924del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477244 | ||||||
| chr5:176477245 | T | C | 1 | a0001c0001t0032g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64-1943T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477245 | |||||||
| chr5:176477245 | T | TTTTTTTT others(129): Show |
1 | a0001c0001t0004g0278 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.64-1926_64-1925ins others(136): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477245 | ||||||
| chr5:176477290 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.64-1898T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477290 | |||||||
| chr5:176477293 | G | A | 1 | a0001c0001t0034g0207 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.64-1895G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477293 | |||||||
| chr5:176477307 | T | G | 277 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(274): Show |
279 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.64-1881T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477307 | |||||||
| chr5:176477345 | C | T | 2 | a0001c0001t0010g0005 a0001c0001t0010g0006 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64-1843C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477345 | |||||||
| chr5:176477417 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.64-1771C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477417 | |||||||
| chr5:176477485 | G | A | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-1703G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477485 | |||||||
| chr5:176477569 | CAAAGCCA others(9): Show |
C | 2 | a0001c0001t0003g0056 a0001c0001t0003g0058 |
2 | NA18963.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.64-1614_64-1599del others(16): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 176477569 | ||||||
| chr5:176477588 | A | G | 1 | a0001c0001t0016g0202 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.64-1600A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176477588 | |||||||
| chr5:176478302 | T | C | 302 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(299): Show |
305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.64-886T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478302 | |||||||
| chr5:176478359 | G | A | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.64-829G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478359 | |||||||
| chr5:176478430 | C | T | 81 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(78): Show |
82 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.64-758C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478430 | |||||||
| chr5:176478446 | T | A | 3 | a0001c0001t0002g0298 a0001c0001t0002g0305 a0001c0001t0002g0324 |
3 | HG00639.hp1 HG01358.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.64-742T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478446 | |||||||
| chr5:176478506 | G | A | 1 | a0001c0001t0004g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64-682G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478506 | |||||||
| chr5:176478510 | G | C | 1 | a0001c0001t0005g0261 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.64-678G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478510 | |||||||
| chr5:176478596 | T | G | 9 | a0001c0001t0001g0118 a0001c0001t0001g0153 a0001c0001t0001g0164 others(6): Show |
9 | HG00621.hp1 HG02071.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-592T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478596 | |||||||
| chr5:176478646 | C | G | 1 | a0001c0001t0005g0269 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.64-542C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478646 | |||||||
| chr5:176478688 | T | C | 1 | a0001c0008t0027g0296 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-500T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478688 | |||||||
| chr5:176478731 | A | G | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-457A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 1/10 | chr5 | 176478731 | |||||||
| chr5:176479695 | G | T | 1 | a0001c0001t0009g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.132+439G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176479695 | |||||||
| chr5:176479756 | G | A | 1 | a0001c0001t0003g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.132+500G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176479756 | |||||||
| chr5:176479883 | C | T | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.132+627C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176479883 | |||||||
| chr5:176479938 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.132+682G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176479938 | |||||||
| chr5:176480195 | G | T | 142 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(139): Show |
143 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.132+939G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480195 | |||||||
| chr5:176480261 | G | A | 1 | a0001c0001t0004g0211 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.132+1005G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480261 | |||||||
| chr5:176480267 | G | A | 1 | a0001c0001t0033g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.132+1011G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480267 | |||||||
| chr5:176480288 | CT | C | 9 | a0001c0001t0002g0004 a0001c0001t0002g0289 a0001c0001t0002g0290 others(6): Show |
10 | HG01993.hp1 NA18945.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.132+1041delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176480288 | ||||||
| chr5:176480523 | C | G | 6 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(3): Show |
7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+1267C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480523 | |||||||
| chr5:176480596 | G | T | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.132+1340G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480596 | |||||||
| chr5:176480712 | C | G | 1 | a0001c0001t0002g0300 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.132+1456C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480712 | |||||||
| chr5:176480769 | C | T | 2 | a0001c0001t0007g0366 a0001c0001t0007g0367 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.132+1513C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480769 | |||||||
| chr5:176480960 | A | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0077 a0001c0001t0003g0361 |
4 | HG01168.hp2 HG02735.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+1704A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176480960 | |||||||
| chr5:176481006 | A | G | 2 | a0001c0001t0013g0020 a0001c0001t0013g0026 |
2 | HG01891.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.132+1750A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481006 | |||||||
| chr5:176481018 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.132+1762G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481018 | |||||||
| chr5:176481139 | C | T | 1 | a0001c0001t0010g0006 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.132+1883C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481139 | |||||||
| chr5:176481236 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0178 |
2 | NA19072.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.132+1980C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481236 | |||||||
| chr5:176481323 | G | A | 1 | a0001c0001t0002g0318 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.132+2067G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481323 | |||||||
| chr5:176481345 | C | T | 1 | a0001c0001t0003g0080 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.132+2089C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481345 | |||||||
| chr5:176481383 | C | T | 2 | a0001c0001t0010g0005 a0001c0001t0010g0006 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.132+2127C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481383 | |||||||
| chr5:176481444 | T | C | 10 | a0001c0001t0004g0003 a0001c0001t0004g0217 a0001c0001t0004g0238 others(7): Show |
11 | HG01361.hp1 HG01891.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.132+2188T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481444 | |||||||
| chr5:176481489 | C | A | 5 | a0001c0001t0006g0262 a0001c0001t0006g0270 a0001c0001t0006g0271 others(2): Show |
5 | HG01496.hp2 HG03209.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+2233C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481489 | |||||||
| chr5:176481610 | A | G | 302 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(299): Show |
305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.132+2354A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481610 | |||||||
| chr5:176481751 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.132+2495G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481751 | |||||||
| chr5:176481797 | G | A | 3 | a0001c0001t0003g0037 a0001c0001t0003g0083 a0001c0001t0003g0089 |
3 | HG00558.hp2 NA18939.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.132+2541G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481797 | |||||||
| chr5:176481802 | C | T | 1 | a0001c0001t0004g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.132+2546C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481802 | |||||||
| chr5:176481824 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.132+2568G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481824 | |||||||
| chr5:176481861 | T | C | 59 | a0001c0001t0004g0242 a0001c0001t0004g0277 a0001c0001t0004g0278 others(56): Show |
59 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.132+2605T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481861 | |||||||
| chr5:176481932 | C | G | 3 | a0002c0002t0001g0163 a0002c0002t0001g0166 a0002c0002t0001g0171 |
3 | NA18974.hp1 NA19066.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.132+2676C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481932 | |||||||
| chr5:176481977 | C | G | 1 | a0001c0001t0021g0335 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.132+2721C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176481977 | |||||||
| chr5:176482051 | C | T | 74 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(71): Show |
76 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.132+2795C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482051 | |||||||
| chr5:176482220 | G | GT | 181 | a0001c0001t0001g0036 a0001c0001t0001g0095 a0001c0001t0001g0104 others(178): Show |
183 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.132+2979dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176482220 | ||||||
| chr5:176482466 | G | A | 1 | a0001c0001t0003g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.132+3210G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482466 | |||||||
| chr5:176482489 | A | C | 76 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(73): Show |
78 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.132+3233A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482489 | |||||||
| chr5:176482640 | C | T | 225 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(222): Show |
226 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.132+3384C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482640 | |||||||
| chr5:176482790 | C | A | 211 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(208): Show |
212 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.132+3534C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482790 | |||||||
| chr5:176482795 | C | T | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.132+3539C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482795 | |||||||
| chr5:176482863 | A | G | 1 | a0001c0001t0004g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.133-3492A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482863 | |||||||
| chr5:176482895 | T | TTTG | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0008g0040 |
3 | HG00408.hp2 NA18965.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.133-3439_133-3437d others(5): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176482895 | ||||||
| chr5:176482895 | TTTGTTG | T | 62 | a0001c0001t0001g0113 a0001c0001t0001g0131 a0001c0001t0001g0345 others(59): Show |
62 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.133-3442_133-3437d others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176482895 | ||||||
| chr5:176482933 | T | C | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.133-3422T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482933 | |||||||
| chr5:176482973 | G | C | 1 | a0001c0001t0003g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.133-3382G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482973 | |||||||
| chr5:176482976 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0178 |
2 | NA19072.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.133-3379C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176482976 | |||||||
| chr5:176483036 | C | CT | 22 | a0001c0001t0002g0323 a0001c0001t0002g0340 a0001c0001t0005g0027 others(19): Show |
22 | HG00544.hp2 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.133-3311dupT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176483036 | ||||||
| chr5:176483044 | T | A | 6 | a0001c0001t0002g0299 a0001c0001t0004g0277 a0001c0001t0004g0278 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-3311T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483044 | |||||||
| chr5:176483080 | G | A | 2 | a0001c0001t0002g0310 a0001c0001t0002g0337 |
2 | NA18995.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.133-3275G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483080 | |||||||
| chr5:176483163 | C | T | 1 | a0001c0001t0005g0263 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.133-3192C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483163 | |||||||
| chr5:176483202 | A | C | 1 | a0001c0001t0034g0207 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.133-3153A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483202 | |||||||
| chr5:176483217 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.133-3138G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483217 | |||||||
| chr5:176483251 | T | C | 127 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(124): Show |
128 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.133-3104T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483251 | |||||||
| chr5:176483675 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.133-2680G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483675 | |||||||
| chr5:176483686 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.133-2669T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483686 | |||||||
| chr5:176483798 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.133-2557C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483798 | |||||||
| chr5:176483799 | G | A | 1 | a0001c0001t0005g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.133-2556G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176483799 | |||||||
| chr5:176484075 | A | T | 1 | a0001c0001t0005g0365 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.133-2280A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484075 | |||||||
| chr5:176484144 | G | A | 1 | a0001c0001t0003g0072 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.133-2211G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484144 | |||||||
| chr5:176484201 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.133-2154G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484201 | |||||||
| chr5:176484311 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.133-2044A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484311 | |||||||
| chr5:176484445 | T | C | 3 | a0001c0001t0002g0349 a0001c0001t0002g0351 a0005c0004t0002g0350 |
3 | HG02451.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.133-1910T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484445 | |||||||
| chr5:176484548 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.133-1807G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484548 | |||||||
| chr5:176484658 | C | T | 74 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(71): Show |
76 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.133-1697C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484658 | |||||||
| chr5:176484693 | C | A | 1 | a0001c0001t0003g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.133-1662C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484693 | |||||||
| chr5:176484806 | G | A | 1 | a0001c0001t0004g0120 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.133-1549G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484806 | |||||||
| chr5:176484870 | C | A | 1 | a0001c0001t0002g0329 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.133-1485C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484870 | |||||||
| chr5:176484894 | G | GA | 70 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0165 others(67): Show |
71 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.133-1446dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176484894 | ||||||
| chr5:176484894 | GA | G | 59 | a0001c0001t0004g0242 a0001c0001t0004g0277 a0001c0001t0004g0278 others(56): Show |
59 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.133-1446delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 176484894 | ||||||
| chr5:176484917 | G | A | 1 | a0001c0001t0003g0032 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.133-1438G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176484917 | |||||||
| chr5:176485145 | C | T | 3 | a0001c0001t0002g0349 a0001c0001t0002g0351 a0005c0004t0002g0350 |
3 | HG02451.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.133-1210C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485145 | |||||||
| chr5:176485223 | C | G | 1 | a0001c0001t0017g0276 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.133-1132C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485223 | |||||||
| chr5:176485276 | A | G | 1 | a0001c0001t0005g0253 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.133-1079A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485276 | |||||||
| chr5:176485330 | A | G | 58 | a0001c0001t0004g0277 a0001c0001t0004g0278 a0001c0001t0004g0279 others(55): Show |
58 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.133-1025A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485330 | |||||||
| chr5:176485754 | G | A | 10 | a0001c0001t0006g0088 a0001c0001t0006g0215 a0001c0001t0006g0220 others(7): Show |
10 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-601G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485754 | |||||||
| chr5:176485779 | G | A | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-576G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485779 | |||||||
| chr5:176485862 | C | T | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.133-493C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485862 | |||||||
| chr5:176485923 | G | A | 1 | a0001c0001t0033g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.133-432G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485923 | |||||||
| chr5:176485993 | G | A | 76 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(73): Show |
78 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.133-362G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176485993 | |||||||
| chr5:176486081 | A | G | 6 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(3): Show |
7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.133-274A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176486081 | |||||||
| chr5:176486305 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.133-50G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176486305 | |||||||
| chr5:176486341 | G | A | 1 | a0001c0001t0017g0276 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.133-14G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 2/10 | chr5 | 176486341 | |||||||
| chr5:176486562 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.267+73C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176486562 | |||||||
| chr5:176486673 | AT | A | 301 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(298): Show |
304 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(301): Show |
intron_variant | MODIFIER | c.267+194delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 176486673 | ||||||
| chr5:176486759 | T | C | 1 | a0001c0001t0002g0336 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.267+270T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176486759 | |||||||
| chr5:176487057 | C | T | 294 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(291): Show |
297 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(294): Show |
intron_variant | MODIFIER | c.267+568C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487057 | |||||||
| chr5:176487215 | C | T | 6 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(3): Show |
7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.267+726C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487215 | |||||||
| chr5:176487223 | C | T | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.267+734C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487223 | |||||||
| chr5:176487234 | G | C | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.267+745G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487234 | |||||||
| chr5:176487364 | G | A | 60 | a0001c0001t0004g0242 a0001c0001t0004g0277 a0001c0001t0004g0278 others(57): Show |
60 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.267+875G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487364 | |||||||
| chr5:176487429 | C | T | 4 | a0001c0001t0004g0136 a0001c0001t0004g0212 a0001c0001t0004g0219 others(1): Show |
4 | HG02109.hp2 HG02647.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+940C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487429 | |||||||
| chr5:176487584 | C | T | 142 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(139): Show |
143 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.267+1095C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487584 | |||||||
| chr5:176487590 | C | T | 1 | a0001c0001t0005g0255 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.267+1101C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487590 | |||||||
| chr5:176487828 | A | C | 1 | a0001c0001t0004g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.268-1123A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176487828 | |||||||
| chr5:176488166 | C | T | 2 | a0001c0001t0010g0005 a0001c0001t0010g0006 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.268-785C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488166 | |||||||
| chr5:176488449 | A | C | 59 | a0001c0001t0004g0242 a0001c0001t0004g0277 a0001c0001t0004g0278 others(56): Show |
59 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.268-502A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488449 | |||||||
| chr5:176488479 | T | C | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.268-472T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488479 | |||||||
| chr5:176488483 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.268-468G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488483 | |||||||
| chr5:176488623 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0172 a0001c0001t0001g0189 |
3 | NA18954.hp2 NA19000.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.268-328G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488623 | |||||||
| chr5:176488711 | C | T | 60 | a0001c0001t0004g0242 a0001c0001t0004g0277 a0001c0001t0004g0278 others(57): Show |
60 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.268-240C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488711 | |||||||
| chr5:176488834 | C | T | 362 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(359): Show |
366 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(363): Show |
intron_variant | MODIFIER | c.268-117C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488834 | |||||||
| chr5:176488854 | T | C | 1 | a0001c0001t0005g0216 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.268-97T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488854 | |||||||
| chr5:176488860 | G | A | 75 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(72): Show |
77 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.268-91G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 3/10 | chr5 | 176488860 | |||||||
| chr5:176489059 | A | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0141 |
2 | HG00642.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.344+32A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489059 | |||||||
| chr5:176489076 | C | A | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.344+49C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489076 | |||||||
| chr5:176489082 | T | C | 60 | a0001c0001t0004g0242 a0001c0001t0004g0277 a0001c0001t0004g0278 others(57): Show |
60 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.344+55T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489082 | |||||||
| chr5:176489154 | C | T | 1 | a0001c0001t0002g0309 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.344+127C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489154 | |||||||
| chr5:176489167 | A | G | 1 | a0001c0001t0004g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.344+140A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489167 | |||||||
| chr5:176489181 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.344+154G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489181 | |||||||
| chr5:176489248 | T | C | 220 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(217): Show |
223 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.344+221T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489248 | |||||||
| chr5:176489292 | T | TC | 43 | a0001c0001t0002g0096 a0001c0001t0002g0288 a0001c0001t0002g0289 others(40): Show |
43 | HG00544.hp2 HG01099.hp2 HG01258.hp1 others(40): Show |
intron_variant | MODIFIER | c.344+274dupC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 176489292 | ||||||
| chr5:176489292 | TC | T | 181 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0001g0110 others(178): Show |
184 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(181): Show |
intron_variant | MODIFIER | c.344+274delC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 176489292 | ||||||
| chr5:176489470 | T | A | 6 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(3): Show |
7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+443T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489470 | |||||||
| chr5:176489640 | C | T | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.344+613C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489640 | |||||||
| chr5:176489715 | T | G | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+688T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176489715 | |||||||
| chr5:176490077 | T | C | 302 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(299): Show |
305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.344+1050T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490077 | |||||||
| chr5:176490078 | G | A | 3 | a0001c0001t0004g0242 a0001c0001t0006g0283 a0001c0001t0022g0268 |
3 | HG02886.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.344+1051G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490078 | |||||||
| chr5:176490087 | G | A | 1 | a0001c0001t0030g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.344+1060G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490087 | |||||||
| chr5:176490227 | C | G | 1 | a0001c0001t0028g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.344+1200C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490227 | |||||||
| chr5:176490234 | C | G | 1 | a0001c0001t0033g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.344+1207C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490234 | |||||||
| chr5:176490236 | G | T | 10 | a0001c0001t0006g0088 a0001c0001t0006g0215 a0001c0001t0006g0220 others(7): Show |
10 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.344+1209G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490236 | |||||||
| chr5:176490276 | A | C | 2 | a0001c0001t0004g0243 a0001c0001t0024g0236 |
2 | HG01361.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.344+1249A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490276 | |||||||
| chr5:176490291 | A | C | 78 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(75): Show |
79 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.344+1264A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490291 | |||||||
| chr5:176490305 | C | T | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.344+1278C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490305 | |||||||
| chr5:176490310 | C | CA | 93 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0121 others(90): Show |
95 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.344+1297dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 176490310 | ||||||
| chr5:176490331 | G | T | 10 | a0001c0001t0006g0088 a0001c0001t0006g0215 a0001c0001t0006g0220 others(7): Show |
10 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.344+1304G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490331 | |||||||
| chr5:176490337 | A | G | 13 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(10): Show |
13 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.344+1310A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490337 | |||||||
| chr5:176490341 | T | C | 3 | a0001c0001t0003g0042 a0001c0001t0003g0073 a0001c0001t0003g0079 |
3 | HG01175.hp2 HG01934.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.344+1314T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490341 | |||||||
| chr5:176490384 | G | A | 11 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(8): Show |
11 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+1357G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490384 | |||||||
| chr5:176490532 | GC | G | 151 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(148): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.344+1507delC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 176490532 | ||||||
| chr5:176490778 | T | C | 1 | a0001c0001t0010g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.345-1416T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490778 | |||||||
| chr5:176490788 | C | A | 91 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(88): Show |
93 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.345-1406C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490788 | |||||||
| chr5:176490857 | G | C | 301 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(298): Show |
304 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(301): Show |
intron_variant | MODIFIER | c.345-1337G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490857 | |||||||
| chr5:176490998 | A | G | 58 | a0001c0001t0004g0277 a0001c0001t0004g0278 a0001c0001t0004g0279 others(55): Show |
58 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.345-1196A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176490998 | |||||||
| chr5:176491047 | A | T | 67 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(64): Show |
68 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.345-1147A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491047 | |||||||
| chr5:176491181 | C | T | 1 | a0001c0001t0006g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.345-1013C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491181 | |||||||
| chr5:176491261 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.345-933T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491261 | |||||||
| chr5:176491643 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0011g0107 a0001c0001t0011g0137 others(1): Show |
4 | HG02165.hp1 NA18969.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-551C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491643 | |||||||
| chr5:176491768 | G | GTA | 10 | a0001c0001t0006g0088 a0001c0001t0006g0215 a0001c0001t0006g0220 others(7): Show |
10 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-424_345-423dup others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 176491768 | ||||||
| chr5:176491877 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.345-317G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491877 | |||||||
| chr5:176491913 | T | C | 1 | a0001c0001t0019g0326 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.345-281T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176491913 | |||||||
| chr5:176492065 | A | C | 2 | a0001c0001t0013g0020 a0001c0001t0013g0026 |
2 | HG01891.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.345-129A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176492065 | |||||||
| chr5:176492095 | C | T | 6 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(3): Show |
7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-99C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 4/10 | chr5 | 176492095 | |||||||
| chr5:176492454 | C | T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.483+122C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492454 | |||||||
| chr5:176492514 | G | T | 1 | a0001c0001t0002g0339 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.483+182G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492514 | |||||||
| chr5:176492605 | C | T | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.483+273C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492605 | |||||||
| chr5:176492638 | C | G | 1 | a0001c0001t0003g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.483+306C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492638 | |||||||
| chr5:176492652 | T | C | 6 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(3): Show |
7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+320T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492652 | |||||||
| chr5:176492708 | G | A | 49 | a0001c0001t0004g0242 a0001c0001t0004g0277 a0001c0001t0004g0278 others(46): Show |
49 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.483+376G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492708 | |||||||
| chr5:176492773 | A | G | 2 | a0001c0001t0004g0238 a0001c0001t0004g0353 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.483+441A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492773 | |||||||
| chr5:176492834 | A | G | 2 | a0001c0001t0010g0019 a0001c0001t0010g0021 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.483+502A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492834 | |||||||
| chr5:176492870 | A | G | 2 | a0001c0001t0001g0229 a0001c0001t0018g0235 |
2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.483+538A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492870 | |||||||
| chr5:176492916 | A | G | 1 | a0001c0001t0002g0315 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.483+584A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492916 | |||||||
| chr5:176492969 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.483+637A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492969 | |||||||
| chr5:176492978 | A | G | 3 | a0001c0001t0002g0309 a0001c0001t0002g0311 a0001c0001t0002g0347 |
3 | HG00280.hp1 HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.483+646A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176492978 | |||||||
| chr5:176493119 | C | G | 90 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(87): Show |
92 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.483+787C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493119 | |||||||
| chr5:176493289 | A | G | 145 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(142): Show |
146 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.484-710A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493289 | |||||||
| chr5:176493401 | C | T | 13 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(10): Show |
13 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-598C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493401 | |||||||
| chr5:176493440 | T | G | 144 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(141): Show |
145 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.484-559T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493440 | |||||||
| chr5:176493489 | C | A | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.484-510C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493489 | |||||||
| chr5:176493501 | A | G | 13 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(10): Show |
13 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-498A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493501 | |||||||
| chr5:176493526 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.484-473G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493526 | |||||||
| chr5:176493723 | T | G | 4 | a0001c0001t0006g0270 a0001c0001t0006g0271 a0001c0001t0006g0272 others(1): Show |
4 | HG01496.hp2 NA18906.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-276T>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493723 | |||||||
| chr5:176493919 | G | A | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.484-80G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 5/10 | chr5 | 176493919 | |||||||
| chr5:176494149 | AGTT | A | 66 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(63): Show |
67 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.570-31_570-29delGT others(1): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 176494149 | ||||||
| chr5:176494350 | A | G | 3 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 |
3 | HG02965.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.661+75A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494350 | |||||||
| chr5:176494385 | G | A | 11 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(8): Show |
11 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.661+110G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494385 | |||||||
| chr5:176494407 | T | A | 11 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(8): Show |
11 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.661+132T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494407 | |||||||
| chr5:176494460 | T | C | 219 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(216): Show |
222 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.661+185T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494460 | |||||||
| chr5:176494461 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0178 |
2 | NA19072.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.661+186G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494461 | |||||||
| chr5:176494565 | A | T | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.661+290A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494565 | |||||||
| chr5:176494712 | G | A | 8 | a0001c0001t0006g0220 a0001c0001t0006g0221 a0001c0001t0006g0222 others(5): Show |
8 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.661+437G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494712 | |||||||
| chr5:176494782 | A | G | 144 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(141): Show |
145 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.661+507A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494782 | |||||||
| chr5:176494911 | G | C | 1 | a0001c0008t0027g0296 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.661+636G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494911 | |||||||
| chr5:176494935 | A | G | 66 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(63): Show |
67 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.661+660A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176494935 | |||||||
| chr5:176495016 | G | A | 1 | a0001c0008t0027g0296 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.661+741G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495016 | |||||||
| chr5:176495024 | CAG | C | 7 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+752_661+753del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 176495024 | ||||||
| chr5:176495154 | G | A | 1 | a0001c0001t0004g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.661+879G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495154 | |||||||
| chr5:176495225 | T | C | 1 | a0001c0001t0004g0233 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.661+950T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495225 | |||||||
| chr5:176495409 | AT | A | 6 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(3): Show |
7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-1068delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 176495409 | ||||||
| chr5:176495505 | C | A | 97 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(94): Show |
99 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.662-981C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495505 | |||||||
| chr5:176495510 | AT | A | 23 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(20): Show |
24 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.662-957delT | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 176495510 | ||||||
| chr5:176495510 | ATT | A | 210 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(207): Show |
211 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.662-958_662-957del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 176495510 | ||||||
| chr5:176495510 | ATTT | A | 69 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0177 others(66): Show |
70 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.662-959_662-957del others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 176495510 | ||||||
| chr5:176495624 | G | A | 7 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-862G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495624 | |||||||
| chr5:176495793 | G | GT | 75 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(72): Show |
77 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.662-693_662-692ins others(1): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495793 | |||||||
| chr5:176495879 | G | A | 1 | a0001c0001t0010g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.662-607G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495879 | |||||||
| chr5:176495954 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.662-532G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176495954 | |||||||
| chr5:176496079 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.662-407C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176496079 | |||||||
| chr5:176496124 | C | G | 13 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(10): Show |
13 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.662-362C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176496124 | |||||||
| chr5:176496139 | C | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0183 |
2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.662-347C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176496139 | |||||||
| chr5:176496353 | G | A | 301 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(298): Show |
304 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(301): Show |
intron_variant | MODIFIER | c.662-133G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176496353 | |||||||
| chr5:176496430 | G | A | 144 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(141): Show |
145 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.662-56G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 7/10 | chr5 | 176496430 | |||||||
| chr5:176496704 | G | A | 1 | a0001c0001t0004g0278 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.839+41G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176496704 | |||||||
| chr5:176496846 | G | C | 8 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(5): Show |
9 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.839+183G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176496846 | |||||||
| chr5:176497039 | G | A | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.839+376G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497039 | |||||||
| chr5:176497047 | G | A | 73 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(70): Show |
75 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.839+384G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497047 | |||||||
| chr5:176497073 | G | A | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.839+410G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497073 | |||||||
| chr5:176497111 | A | G | 1 | a0001c0001t0002g0344 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.839+448A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497111 | |||||||
| chr5:176497138 | T | C | 302 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(299): Show |
305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.839+475T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497138 | |||||||
| chr5:176497249 | T | TA | 19 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(16): Show |
20 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.839+596dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 176497249 | ||||||
| chr5:176497297 | T | A | 7 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.839+634T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497297 | |||||||
| chr5:176497366 | A | T | 306 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(303): Show |
309 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.839+703A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497366 | |||||||
| chr5:176497374 | C | G | 1 | a0001c0001t0003g0052 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.839+711C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497374 | |||||||
| chr5:176497401 | T | A | 3 | a0001c0001t0003g0041 a0001c0001t0003g0054 a0001c0001t0003g0067 |
3 | HG03654.hp2 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.839+738T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497401 | |||||||
| chr5:176497410 | A | G | 2 | a0001c0001t0003g0051 a0001c0001t0003g0057 |
2 | HG00558.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.839+747A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497410 | |||||||
| chr5:176497421 | A | G | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.839+758A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497421 | |||||||
| chr5:176497872 | G | A | 1 | a0001c0001t0005g0269 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.840-1042G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176497872 | |||||||
| chr5:176498220 | C | T | 65 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(62): Show |
66 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.840-694C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176498220 | |||||||
| chr5:176498408 | TTG | T | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.840-504_840-503del others(2): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 176498408 | ||||||
| chr5:176498820 | T | TAC | 3 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 |
3 | NA18990.hp2 NA19002.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.840-78_840-77dupCA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 176498820 | ||||||
| chr5:176498848 | A | G | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.840-66A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176498848 | |||||||
| chr5:176498911 | C | T | 1 | a0001c0001t0003g0053 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.840-3C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 8/10 | chr5 | 176498911 | |||||||
| chr5:176499317 | G | A | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1011+232G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499317 | |||||||
| chr5:176499382 | C | T | 1 | a0001c0001t0017g0276 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1011+297C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499382 | |||||||
| chr5:176499600 | T | C | 86 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(83): Show |
88 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1012-403T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499600 | |||||||
| chr5:176499656 | A | G | 2 | a0001c0001t0005g0255 a0001c0001t0005g0259 |
2 | NA18946.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1012-347A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499656 | |||||||
| chr5:176499745 | G | C | 302 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(299): Show |
305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.1012-258G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499745 | |||||||
| chr5:176499792 | C | T | 2 | a0001c0001t0002g0306 a0006c0007t0002g0330 |
2 | HG03688.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1012-211C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 9/10 | chr5 | 176499792 | |||||||
| chr5:176500261 | C | CAG | 20 | a0001c0001t0006g0088 a0001c0001t0006g0215 a0001c0001t0006g0220 others(17): Show |
20 | HG00642.hp2 HG01099.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1155+133_1155+134d others(4): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176500261 | ||||||
| chr5:176500307 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1155+161A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176500307 | |||||||
| chr5:176500362 | A | G | 1 | a0001c0001t0003g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1155+216A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176500362 | |||||||
| chr5:176500528 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1155+382C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176500528 | |||||||
| chr5:176500617 | C | T | 9 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+471C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176500617 | |||||||
| chr5:176500780 | TAGTC | T | 10 | a0001c0001t0004g0003 a0001c0001t0004g0218 a0001c0001t0004g0238 others(7): Show |
11 | HG01361.hp1 HG01891.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.1155+638_1155+641d others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176500780 | ||||||
| chr5:176500893 | G | A | 1 | a0001c0001t0002g0336 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1155+747G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176500893 | |||||||
| chr5:176501052 | G | A | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1155+906G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501052 | |||||||
| chr5:176501092 | A | G | 1 | a0001c0001t0005g0253 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1155+946A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501092 | |||||||
| chr5:176501128 | A | T | 3 | a0001c0001t0004g0136 a0001c0001t0006g0283 a0001c0001t0026g0092 |
3 | HG02109.hp2 HG02132.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1155+982A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501128 | |||||||
| chr5:176501132 | T | A | 12 | a0001c0001t0004g0242 a0001c0001t0005g0362 a0001c0001t0006g0271 others(9): Show |
13 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1155+986T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501132 | |||||||
| chr5:176501133 | A | T | 8 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(5): Show |
9 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+987A>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501133 | |||||||
| chr5:176501133 | AAATAAT | A | 67 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(64): Show |
68 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1155+998_1155+1003 others(9): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176501133 | ||||||
| chr5:176501305 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1155+1159G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501305 | |||||||
| chr5:176501382 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1155+1236G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501382 | |||||||
| chr5:176501557 | C | T | 1 | a0001c0001t0033g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1155+1411C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501557 | |||||||
| chr5:176501564 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1155+1418G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501564 | |||||||
| chr5:176501967 | G | A | 1 | a0001c0001t0004g0212 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1155+1821G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501967 | |||||||
| chr5:176501976 | C | T | 202 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(199): Show |
203 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.1155+1830C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176501976 | |||||||
| chr5:176502101 | C | T | 302 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(299): Show |
305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.1155+1955C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502101 | |||||||
| chr5:176502151 | C | T | 1 | a0001c0001t0006g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1155+2005C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502151 | |||||||
| chr5:176502237 | C | T | 1 | a0001c0001t0002g0289 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1155+2091C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502237 | |||||||
| chr5:176502256 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1155+2110A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502256 | |||||||
| chr5:176502309 | T | C | 1 | a0001c0001t0005g0257 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1155+2163T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502309 | |||||||
| chr5:176502346 | C | T | 12 | a0001c0001t0004g0120 a0001c0001t0004g0149 a0001c0001t0004g0169 others(9): Show |
12 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1155+2200C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502346 | |||||||
| chr5:176502468 | G | T | 76 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(73): Show |
78 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1155+2322G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502468 | |||||||
| chr5:176502499 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1155+2353G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502499 | |||||||
| chr5:176502521 | G | A | 1 | a0001c0001t0004g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1155+2375G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502521 | |||||||
| chr5:176502838 | A | G | 1 | a0001c0001t0003g0071 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1155+2692A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502838 | |||||||
| chr5:176502997 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1155+2851G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176502997 | |||||||
| chr5:176503047 | CA | C | 76 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0111 others(73): Show |
78 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1155+2911delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176503047 | ||||||
| chr5:176503277 | G | A | 13 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(10): Show |
13 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1155+3131G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503277 | |||||||
| chr5:176503329 | C | T | 6 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(3): Show |
7 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1155+3183C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503329 | |||||||
| chr5:176503381 | C | T | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1155+3235C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503381 | |||||||
| chr5:176503486 | C | T | 2 | a0001c0001t0013g0020 a0001c0001t0013g0026 |
2 | HG01891.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1156-3282C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503486 | |||||||
| chr5:176503487 | G | A | 143 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0106 others(140): Show |
144 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.1156-3281G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503487 | |||||||
| chr5:176503555 | CA | C | 272 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(269): Show |
275 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.1156-3196delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176503555 | ||||||
| chr5:176503555 | CAA | C | 13 | a0001c0001t0001g0153 a0001c0001t0003g0052 a0001c0001t0003g0069 others(10): Show |
13 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1156-3197_1156-319 others(6): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176503555 | ||||||
| chr5:176503884 | G | A | 1 | a0001c0001t0013g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1156-2884G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503884 | |||||||
| chr5:176503884 | G | C | 67 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(64): Show |
68 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1156-2884G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176503884 | |||||||
| chr5:176504056 | G | A | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1156-2712G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504056 | |||||||
| chr5:176504128 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1156-2640C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504128 | |||||||
| chr5:176504228 | G | C | 302 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(299): Show |
305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.1156-2540G>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504228 | |||||||
| chr5:176504247 | G | A | 1 | a0001c0001t0004g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1156-2521G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504247 | |||||||
| chr5:176504305 | C | T | 1 | a0001c0001t0006g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1156-2463C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504305 | |||||||
| chr5:176504325 | C | T | 1 | a0001c0001t0002g0347 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1156-2443C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504325 | |||||||
| chr5:176504451 | G | T | 1 | a0001c0001t0005g0365 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1156-2317G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504451 | |||||||
| chr5:176504456 | C | T | 1 | a0001c0001t0022g0268 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1156-2312C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504456 | |||||||
| chr5:176504498 | C | T | 2 | a0001c0001t0010g0019 a0001c0001t0010g0021 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1156-2270C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504498 | |||||||
| chr5:176504532 | C | T | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1156-2236C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504532 | |||||||
| chr5:176504743 | G | T | 1 | a0001c0008t0027g0296 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1156-2025G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504743 | |||||||
| chr5:176504769 | C | T | 301 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(298): Show |
304 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(301): Show |
intron_variant | MODIFIER | c.1156-1999C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504769 | |||||||
| chr5:176504921 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1156-1847G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176504921 | |||||||
| chr5:176505001 | C | T | 7 | a0001c0001t0003g0002 a0001c0001t0003g0074 a0001c0001t0003g0075 others(4): Show |
8 | HG01081.hp2 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1156-1767C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505001 | |||||||
| chr5:176505009 | C | T | 66 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(63): Show |
67 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1156-1759C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505009 | |||||||
| chr5:176505010 | A | G | 362 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(359): Show |
366 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(363): Show |
intron_variant | MODIFIER | c.1156-1758A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505010 | |||||||
| chr5:176505013 | AC | A | 75 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(72): Show |
76 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1156-1753delC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176505013 | ||||||
| chr5:176505015 | C | G | 75 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0002 others(72): Show |
76 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1156-1753C>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505015 | |||||||
| chr5:176505023 | G | GA | 7 | a0001c0001t0001g0113 a0001c0001t0001g0155 a0001c0001t0002g0347 others(4): Show |
7 | HG01081.hp1 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1156-1727dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176505023 | ||||||
| chr5:176505023 | GA | G | 71 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0147 others(68): Show |
72 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1156-1727delA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176505023 | ||||||
| chr5:176505024 | A | G | 2 | a0001c0001t0007g0018 a0006c0007t0002g0330 |
2 | HG02896.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1156-1744A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505024 | |||||||
| chr5:176505213 | A | G | 1 | a0001c0001t0010g0006 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1156-1555A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505213 | |||||||
| chr5:176505375 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1156-1393T>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505375 | |||||||
| chr5:176505455 | A | G | 9 | a0001c0001t0001g0113 a0001c0001t0009g0097 a0001c0001t0009g0099 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1156-1313A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505455 | |||||||
| chr5:176505467 | G | A | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1156-1301G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505467 | |||||||
| chr5:176505646 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG01975.hp1 HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1156-1122A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505646 | |||||||
| chr5:176505692 | A | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0131 a0001c0001t0004g0219 |
3 | HG02976.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1156-1076A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505692 | |||||||
| chr5:176505703 | G | A | 2 | a0001c0001t0014g0014 a0001c0001t0014g0015 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1156-1065G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505703 | |||||||
| chr5:176505709 | T | C | 4 | a0001c0001t0001g0118 a0001c0001t0001g0153 a0001c0001t0001g0199 others(1): Show |
4 | NA18612.hp1 NA18939.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1156-1059T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505709 | |||||||
| chr5:176505957 | G | A | 1 | a0001c0001t0010g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1156-811G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176505957 | |||||||
| chr5:176506024 | G | A | 302 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(299): Show |
305 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.1156-744G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506024 | |||||||
| chr5:176506034 | C | T | 5 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1156-734C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506034 | |||||||
| chr5:176506059 | C | T | 147 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(144): Show |
148 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1156-709C>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506059 | |||||||
| chr5:176506192 | C | CA | 13 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0167 others(10): Show |
13 | HG00423.hp2 HG00438.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1156-562dupA | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176506192 | ||||||
| chr5:176506194 | AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(1): Show |
4 | NA18955.hp2 NA18990.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-560_1156-548d others(15): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176506194 | ||||||
| chr5:176506201 | A | AC | 3 | a0001c0001t0010g0005 a0001c0001t0010g0006 a0001c0001t0010g0021 |
3 | HG02486.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1156-567_1156-566i others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506201 | |||||||
| chr5:176506204 | A | AC | 20 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(17): Show |
20 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1156-564_1156-563i others(3): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506204 | |||||||
| chr5:176506204 | A | C | 10 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(7): Show |
11 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1156-564A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506204 | |||||||
| chr5:176506205 | A | C | 66 | a0001c0001t0001g0204 a0001c0001t0003g0002 a0001c0001t0003g0028 others(63): Show |
67 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1156-563A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506205 | |||||||
| chr5:176506206 | AC | A | 7 | a0001c0001t0007g0001 a0001c0001t0007g0016 a0001c0001t0007g0017 others(4): Show |
8 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1156-561delC | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506206 | |||||||
| chr5:176506207 | C | A | 74 | a0001c0001t0001g0139 a0001c0001t0001g0174 a0001c0001t0001g0204 others(71): Show |
75 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1156-561C>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506207 | |||||||
| chr5:176506208 | A | C | 1 | a0001c0001t0005g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1156-560A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506208 | |||||||
| chr5:176506209 | A | C | 73 | a0001c0001t0001g0204 a0001c0001t0003g0002 a0001c0001t0003g0028 others(70): Show |
75 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1156-559A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506209 | |||||||
| chr5:176506210 | A | C | 10 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(7): Show |
10 | HG01243.hp1 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1156-558A>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506210 | |||||||
| chr5:176506359 | A | G | 1 | a0001c0001t0033g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1156-409A>G | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506359 | |||||||
| chr5:176506543 | G | T | 7 | a0001c0001t0009g0097 a0001c0001t0009g0099 a0001c0001t0009g0100 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1156-225G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506543 | |||||||
| chr5:176506588 | T | C | 1 | a0001c0008t0027g0296 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1156-180T>C | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506588 | |||||||
| chr5:176506690 | TGTGTGTG others(1): Show |
T | 203 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0095 others(200): Show |
204 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1156-62_1156-55del others(8): Show |
FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 176506690 | ||||||
| chr5:176506699 | G | T | 4 | a0001c0001t0005g0027 a0001c0001t0005g0260 a0001c0001t0005g0266 others(1): Show |
4 | NA18953.hp1 NA18965.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1156-69G>T | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506699 | |||||||
| chr5:176506707 | G | A | 1 | a0001c0001t0005g0103 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1156-61G>A | FAF2 | ENSG00000113194.13 | transcript | ENST00000261942.7 | protein_coding | 10/10 | chr5 | 176506707 |