Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3267 |
| ensemblid | ENSG00000173744.18 |
| hgncid | 5175 |
| symbol | AGFG1 |
| name | ArfGAP with FG repeats 1 |
| refseq_nuc | NM_004504.5 |
| refseq_prot | NP_004495.2 |
| ensembl_nuc | ENST00000310078.13 |
| ensembl_prot | ENSP00000312059.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 227472156 |
| end | 227561217 |
| strand | + |
| ver | v1.2 |
| region | chr2:227472156-227561217 |
| region5000 | chr2:227467156-227566217 |
| regionname0 | AGFG1_chr2_227472156_227561217 |
| regionname5000 | AGFG1_chr2_227467156_227566217 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 562 | 325 | 91 | 44 | 138 | 10 | 40 | 100 | AGFG1_chr2_227467156_227566217 | AGFG1 | MAASA others(557): Show |
chr2 | 227467156 | 227566217 |
| a0002 | 0/0 | 562 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | MAASA others(557): Show |
chr2 | 227467156 | 227566217 |
| a0003 | 0/0 | 562 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | MAASA others(557): Show |
chr2 | 227467156 | 227566217 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1686 | 196 | 63 | 28 | 75 | 7 | 22 | AGFG1_chr2_227467156_227566217 | AGFG1 | ATGGC others(1681): Show |
chr2 | 227467156 | 227566217 | ||
| a0001c0002 | 1/0 | 1686 | 78 | 14 | 8 | 43 | 2 | 10 | AGFG1_chr2_227467156_227566217 | AGFG1 | ATGGC others(1681): Show |
chr2 | 227467156 | 227566217 | ||
| a0001c0003 | 0/0 | 1686 | 28 | 0 | 7 | 15 | 1 | 5 | AGFG1_chr2_227467156_227566217 | AGFG1 | ATGGC others(1681): Show |
chr2 | 227467156 | 227566217 | ||
| a0001c0004 | 0/0 | 1686 | 21 | 12 | 1 | 5 | 0 | 3 | AGFG1_chr2_227467156_227566217 | AGFG1 | ATGGC others(1681): Show |
chr2 | 227467156 | 227566217 | ||
| a0001c0005 | 0/0 | 1686 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | ATGGC others(1681): Show |
chr2 | 227467156 | 227566217 | ||
| a0002c0006 | 0/0 | 1686 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | ATGGC others(1681): Show |
chr2 | 227467156 | 227566217 | ||
| a0002c0007 | 0/0 | 1686 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | ATGGC others(1681): Show |
chr2 | 227467156 | 227566217 | ||
| a0003c0008 | 0/0 | 1686 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | ATGGC others(1681): Show |
chr2 | 227467156 | 227566217 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8677 | 122 | 25 | 15 | 67 | 2 | 13 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0004 | 0/1 | 8677 | 16 | 1 | 6 | 2 | 3 | 3 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0005 | 0/0 | 8677 | 15 | 10 | 3 | 0 | 2 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0008 | 0/0 | 8673 | 7 | 1 | 2 | 0 | 0 | 4 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8668): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0010 | 0/0 | 8677 | 4 | 3 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0011 | 0/0 | 8677 | 3 | 2 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0012 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0015 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0016 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0017 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0018 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0019 | 0/0 | 8677 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0020 | 0/0 | 8677 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0021 | 0/0 | 8681 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8676): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0023 | 0/0 | 8673 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8668): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0025 | 0/0 | 8677 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0026 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0027 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0030 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0031 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0032 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0033 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0037 | 0/0 | 8677 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0038 | 0/0 | 8677 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0040 | 0/0 | 8677 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0001t0041 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8676): Show |
chr2 | 227467156 | 227566217 |
| a0001c0002t0002 | 0/0 | 8678 | 63 | 7 | 5 | 41 | 2 | 8 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8673): Show |
chr2 | 227467156 | 227566217 |
| a0001c0002t0007 | 0/0 | 8677 | 7 | 5 | 2 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0002t0022 | 1/0 | 8677 | 2 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0002t0024 | 0/0 | 8678 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8673): Show |
chr2 | 227467156 | 227566217 |
| a0001c0002t0028 | 0/0 | 8678 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8673): Show |
chr2 | 227467156 | 227566217 |
| a0001c0002t0029 | 0/0 | 8678 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8673): Show |
chr2 | 227467156 | 227566217 |
| a0001c0002t0034 | 0/0 | 8678 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8673): Show |
chr2 | 227467156 | 227566217 |
| a0001c0002t0035 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0001c0002t0036 | 0/0 | 8678 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8673): Show |
chr2 | 227467156 | 227566217 |
| a0001c0003t0003 | 0/0 | 8680 | 25 | 0 | 7 | 13 | 1 | 4 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8675): Show |
chr2 | 227467156 | 227566217 |
| a0001c0003t0013 | 0/0 | 8681 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8676): Show |
chr2 | 227467156 | 227566217 |
| a0001c0003t0039 | 0/0 | 8680 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8675): Show |
chr2 | 227467156 | 227566217 |
| a0001c0004t0006 | 0/0 | 8681 | 14 | 6 | 1 | 4 | 0 | 3 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8676): Show |
chr2 | 227467156 | 227566217 |
| a0001c0004t0009 | 0/0 | 8681 | 6 | 6 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8676): Show |
chr2 | 227467156 | 227566217 |
| a0001c0004t0042 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8676): Show |
chr2 | 227467156 | 227566217 |
| a0001c0005t0014 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0002c0006t0002 | 0/0 | 8678 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8673): Show |
chr2 | 227467156 | 227566217 |
| a0002c0007t0012 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8672): Show |
chr2 | 227467156 | 227566217 |
| a0003c0008t0013 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | CCCCT others(8676): Show |
chr2 | 227467156 | 227566217 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0008g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0008g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0010g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0011g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0015g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0015g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0016g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0016g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0017g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0017g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0018g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0018g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0019g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0019g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0020g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0020g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0021g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0021g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0023g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0023g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0025g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0026g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0027g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0030g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0031g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0032g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0033g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0037g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0038g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0040g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0001t0041g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0007g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0007g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0022g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0022g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0024g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0028g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0029g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0034g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0035g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0002t0036g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0013g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0013g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0003t0039g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0004t0042g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0005t0014g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0001c0005t0014g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0002c0006t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0002c0007t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| a0003c0008t0013g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0003 | g0074 | EUR | GBR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0187 | EUR | GBR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00423 | hp1 | a0001 | c0003 | t0003 | g0076 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00609 | hp2 | a0001 | c0003 | t0003 | g0075 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00639 | hp1 | a0001 | c0001 | t0008 | g0026 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00639 | hp2 | a0001 | c0001 | t0011 | g0094 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0120 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00738 | hp2 | a0001 | c0004 | t0006 | g0049 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG00741 | hp2 | a0001 | c0001 | t0037 | g0118 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0273 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0282 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0198 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0027 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0284 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0283 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01243 | hp1 | a0001 | c0002 | t0007 | g0006 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01243 | hp2 | a0001 | c0002 | t0024 | g0272 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01255 | hp1 | a0001 | c0002 | t0007 | g0091 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0117 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0258 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0223 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0307 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0193 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0254 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0308 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01884 | hp1 | a0001 | c0002 | t0007 | g0006 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0192 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01934 | hp2 | a0001 | c0003 | t0003 | g0064 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01952 | hp2 | a0001 | c0003 | t0003 | g0059 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01993 | hp2 | a0001 | c0003 | t0003 | g0057 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0083 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02015 | hp1 | a0001 | c0001 | t0020 | g0152 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0294 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0286 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02074 | hp1 | a0001 | c0003 | t0003 | g0065 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02129 | hp1 | a0001 | c0004 | t0042 | g0039 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02135 | hp1 | a0001 | c0004 | t0006 | g0054 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02145 | hp1 | a0001 | c0002 | t0035 | g0088 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0276 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02273 | hp1 | a0001 | c0003 | t0003 | g0058 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02293 | hp2 | a0001 | c0003 | t0003 | g0069 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02451 | hp1 | a0001 | c0004 | t0006 | g0040 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02523 | hp1 | a0001 | c0003 | t0003 | g0067 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0277 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0251 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02615 | hp2 | a0001 | c0004 | t0009 | g0047 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02622 | hp1 | a0001 | c0001 | t0018 | g0031 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0310 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02630 | hp2 | a0001 | c0001 | t0032 | g0096 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02647 | hp1 | a0001 | c0001 | t0033 | g0178 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02647 | hp2 | a0001 | c0001 | t0026 | g0227 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0312 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0311 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02723 | hp1 | a0001 | c0004 | t0009 | g0046 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02723 | hp2 | a0001 | c0001 | t0041 | g0086 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0055 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0241 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0305 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0287 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02886 | hp1 | a0001 | c0002 | t0007 | g0089 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02895 | hp2 | a0001 | c0001 | t0023 | g0028 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0033 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02896 | hp2 | a0001 | c0004 | t0009 | g0048 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02897 | hp1 | a0001 | c0001 | t0023 | g0024 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0034 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02922 | hp1 | a0001 | c0002 | t0022 | g0061 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0302 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02965 | hp1 | a0001 | c0004 | t0006 | g0004 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0304 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02976 | hp1 | a0001 | c0004 | t0009 | g0043 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03017 | hp1 | a0001 | c0003 | t0039 | g0079 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03041 | hp1 | a0002 | c0007 | t0012 | g0190 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0285 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03098 | hp1 | a0001 | c0001 | t0021 | g0234 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03098 | hp2 | a0001 | c0002 | t0007 | g0090 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03130 | hp1 | a0001 | c0004 | t0006 | g0004 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03195 | hp2 | a0001 | c0001 | t0021 | g0233 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0231 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03225 | hp1 | a0001 | c0001 | t0031 | g0191 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03225 | hp2 | a0001 | c0001 | t0027 | g0238 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0211 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03239 | hp2 | a0001 | c0003 | t0003 | g0060 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0300 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03453 | hp2 | a0001 | c0005 | t0014 | g0029 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0021 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03491 | hp1 | a0001 | c0004 | t0006 | g0005 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03492 | hp1 | a0001 | c0004 | t0006 | g0005 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0022 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0309 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0306 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0299 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03579 | hp1 | a0001 | c0004 | t0006 | g0042 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03654 | hp1 | a0001 | c0002 | t0036 | g0274 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03654 | hp2 | a0001 | c0001 | t0008 | g0037 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0268 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0259 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0097 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0280 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03834 | hp2 | a0001 | c0002 | t0028 | g0296 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03942 | hp2 | a0001 | c0003 | t0003 | g0073 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0279 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG04115 | hp2 | a0001 | c0001 | t0010 | g0036 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG04199 | hp1 | a0001 | c0003 | t0003 | g0078 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0257 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG04204 | hp2 | a0001 | c0004 | t0006 | g0052 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG04228 | hp1 | a0001 | c0001 | t0038 | g0116 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0228 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18522 | hp2 | a0001 | c0004 | t0009 | g0045 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | CHB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18906 | hp1 | a0001 | c0001 | t0015 | g0236 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18906 | hp2 | a0001 | c0001 | t0030 | g0239 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18940 | hp1 | a0002 | c0006 | t0002 | g0252 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18943 | hp1 | a0001 | c0003 | t0013 | g0082 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18944 | hp1 | a0001 | c0003 | t0013 | g0072 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18946 | hp1 | a0003 | c0008 | t0013 | g0080 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18947 | hp2 | a0001 | c0003 | t0003 | g0071 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18949 | hp1 | a0001 | c0003 | t0003 | g0066 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18950 | hp1 | a0001 | c0001 | t0025 | g0220 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18957 | hp2 | a0001 | c0003 | t0003 | g0063 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18960 | hp1 | a0001 | c0004 | t0006 | g0038 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18962 | hp1 | a0001 | c0003 | t0003 | g0081 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18966 | hp2 | a0001 | c0004 | t0006 | g0050 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18969 | hp2 | a0001 | c0002 | t0029 | g0263 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18975 | hp1 | a0001 | c0002 | t0034 | g0253 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18985 | hp2 | a0001 | c0001 | t0020 | g0162 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18986 | hp2 | a0001 | c0003 | t0003 | g0062 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18989 | hp1 | a0001 | c0001 | t0019 | g0165 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19007 | hp2 | a0001 | c0001 | t0040 | g0142 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19009 | hp1 | a0001 | c0003 | t0003 | g0077 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19030 | hp2 | a0001 | c0005 | t0014 | g0030 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0035 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0301 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19057 | hp2 | a0001 | c0003 | t0003 | g0084 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19065 | hp2 | a0001 | c0004 | t0006 | g0053 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19083 | hp1 | a0001 | c0003 | t0003 | g0085 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19085 | hp2 | a0001 | c0003 | t0003 | g0068 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19090 | hp1 | a0001 | c0001 | t0019 | g0199 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19240 | hp1 | a0001 | c0002 | t0007 | g0093 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA19240 | hp2 | a0001 | c0001 | t0017 | g0229 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0249 | EUR | TSI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0134 | EUR | TSI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA20905 | hp1 | a0001 | c0001 | t0008 | g0025 | SAS | GIH | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | GIH | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG01123 | hp2 | a0001 | c0003 | t0003 | g0070 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02109 | hp2 | a0001 | c0004 | t0006 | g0041 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02486 | hp2 | a0001 | c0002 | t0007 | g0092 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02559 | hp1 | a0001 | c0001 | t0012 | g0189 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG02559 | hp2 | a0001 | c0001 | t0018 | g0032 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0235 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG03471 | hp2 | a0001 | c0004 | t0009 | g0044 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | USA | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| HG06807 | hp2 | a0001 | c0004 | t0006 | g0051 | AFR | USA | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0188 | AFR | USA | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0303 | AFR | USA | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| NA21309 | hp2 | a0001 | c0001 | t0011 | g0226 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0119 | REF | REF | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0022 | g0056 | REF | REF | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227533711 | A | G | 1 | a0003 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.977A>G | p.Lys326Arg | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/13 | 1243/8677 | 977/1689 | 326/562 | chr2 | 227533711 | |||
| chr2:227533738 | A | G | 1 | a0002 | 2 | HG03041.hp1 NA18940.hp1 |
missense_variant | MODERATE | c.1004A>G | p.Asn335Ser | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/13 | 1270/8677 | 1004/1689 | 335/562 | chr2 | 227533738 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227520019 | A | G | 1 | a0001c0004 | 21 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(18): Show |
synonymous_variant | LOW | c.333A>G | p.Gln111Gln | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/13 | 599/8677 | 333/1689 | 111/562 | chr2 | 227520019 | |||
| chr2:227533706 | A | G | 2 | a0001c0003 a0003c0008 |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
synonymous_variant | LOW | c.972A>G | p.Ala324Ala | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/13 | 1238/8677 | 972/1689 | 324/562 | chr2 | 227533706 | |||
| chr2:227536953 | T | G | 1 | a0001c0005 | 2 | HG03453.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.1338T>G | p.Ser446Ser | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/13 | 1604/8677 | 1338/1689 | 446/562 | chr2 | 227536953 | |||
| chr2:227551996 | A | G | 4 | a0001c0001 a0001c0004 a0001c0005 others(1): Show |
219 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(216): Show |
synonymous_variant | LOW | c.1416A>G | p.Thr472Thr | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/13 | 1682/8677 | 1416/1689 | 472/562 | chr2 | 227551996 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227472184 | G | A | 1 | a0001c0002t0024 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-238G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/13 | 238 | chr2 | 227472184 | ||||||
| chr2:227472195 | G | A | 1 | a0001c0001t0025 | 1 | NA18950.hp1 | 5_prime_UTR_variant | MODIFIER | c.-227G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/13 | 227 | chr2 | 227472195 | ||||||
| chr2:227472225 | C | T | 1 | a0001c0004t0042 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-197C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/13 | 197 | chr2 | 227472225 | ||||||
| chr2:227472263 | G | A | 2 | a0001c0001t0011 a0001c0001t0026 |
4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-159G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/13 | 159 | chr2 | 227472263 | ||||||
| chr2:227472334 | G | A | 1 | a0001c0005t0014 | 2 | HG03453.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-88G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/13 | 88 | chr2 | 227472334 | ||||||
| chr2:227554657 | C | T | 4 | a0001c0001t0041 a0001c0004t0006 a0001c0004t0009 others(1): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*162C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 162 | chr2 | 227554657 | ||||||
| chr2:227554686 | T | C | 1 | a0001c0001t0015 | 2 | HG03471.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*191T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 191 | chr2 | 227554686 | ||||||
| chr2:227555019 | A | G | 1 | a0001c0001t0040 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*524A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 524 | chr2 | 227555019 | ||||||
| chr2:227555048 | A | T | 4 | a0001c0001t0041 a0001c0004t0006 a0001c0004t0009 others(1): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*553A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 553 | chr2 | 227555048 | ||||||
| chr2:227555347 | T | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*852T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 852 | chr2 | 227555347 | ||||||
| chr2:227555348 | C | T | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 853 | chr2 | 227555348 | ||||||
| chr2:227555349 | T | G | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*854T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 854 | chr2 | 227555349 | ||||||
| chr2:227555350 | T | G | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*855T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 855 | chr2 | 227555350 | ||||||
| chr2:227555352 | G | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*857G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 857 | chr2 | 227555352 | ||||||
| chr2:227555353 | C | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*858C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 858 | chr2 | 227555353 | ||||||
| chr2:227555355 | G | T | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*860G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 860 | chr2 | 227555355 | ||||||
| chr2:227555358 | T | G | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*863T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 863 | chr2 | 227555358 | ||||||
| chr2:227555375 | T | C | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*880T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 880 | chr2 | 227555375 | ||||||
| chr2:227555377 | G | T | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*882G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 882 | chr2 | 227555377 | ||||||
| chr2:227555380 | T | C | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*885T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 885 | chr2 | 227555380 | ||||||
| chr2:227555381 | A | C | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*886A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 886 | chr2 | 227555381 | ||||||
| chr2:227555382 | T | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*887T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 887 | chr2 | 227555382 | ||||||
| chr2:227555383 | A | C | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*888A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 888 | chr2 | 227555383 | ||||||
| chr2:227555404 | G | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 909 | chr2 | 227555404 | ||||||
| chr2:227555405 | T | G | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 910 | chr2 | 227555405 | ||||||
| chr2:227555413 | A | T | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*918A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 918 | chr2 | 227555413 | ||||||
| chr2:227555415 | T | G | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*920T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 920 | chr2 | 227555415 | ||||||
| chr2:227555427 | T | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*932T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 932 | chr2 | 227555427 | ||||||
| chr2:227555446 | A | C | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*951A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 951 | chr2 | 227555446 | ||||||
| chr2:227555448 | A | T | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*953A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 953 | chr2 | 227555448 | ||||||
| chr2:227555468 | A | AT | 4 | a0001c0001t0041 a0001c0004t0006 a0001c0004t0009 others(1): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*981dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 982 | INFO_REALIGN_3_PRIME | chr2 | 227555468 | |||||
| chr2:227555477 | A | T | 7 | a0001c0001t0004 a0001c0001t0037 a0001c0001t0038 others(4): Show |
46 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*982A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 982 | chr2 | 227555477 | ||||||
| chr2:227555587 | T | C | 4 | a0001c0001t0041 a0001c0004t0006 a0001c0004t0009 others(1): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1092T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1092 | chr2 | 227555587 | ||||||
| chr2:227555678 | T | C | 2 | a0001c0001t0005 a0001c0001t0016 |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1183T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1183 | chr2 | 227555678 | ||||||
| chr2:227555935 | A | G | 1 | a0001c0002t0036 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1440A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1440 | chr2 | 227555935 | ||||||
| chr2:227556025 | G | A | 1 | a0001c0002t0028 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1530G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1530 | chr2 | 227556025 | ||||||
| chr2:227556174 | A | T | 1 | a0001c0001t0023 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1679A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1679 | chr2 | 227556174 | ||||||
| chr2:227556230 | G | C | 1 | a0001c0002t0029 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1735G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1735 | chr2 | 227556230 | ||||||
| chr2:227556491 | A | G | 2 | a0001c0001t0008 a0001c0001t0023 |
9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1996A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1996 | chr2 | 227556491 | ||||||
| chr2:227556495 | C | T | 4 | a0001c0001t0041 a0001c0004t0006 a0001c0004t0009 others(1): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2000C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2000 | chr2 | 227556495 | ||||||
| chr2:227556510 | T | C | 1 | a0001c0001t0017 | 2 | HG03209.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2015T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2015 | chr2 | 227556510 | ||||||
| chr2:227556554 | G | A | 1 | a0001c0001t0017 | 2 | HG03209.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2059G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2059 | chr2 | 227556554 | ||||||
| chr2:227556745 | G | C | 5 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0018 others(2): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2250G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2250 | chr2 | 227556745 | ||||||
| chr2:227556747 | G | A | 1 | a0001c0001t0019 | 2 | NA18989.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2252G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2252 | chr2 | 227556747 | ||||||
| chr2:227556758 | A | G | 2 | a0001c0002t0007 a0001c0002t0035 |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2263A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2263 | chr2 | 227556758 | ||||||
| chr2:227556856 | C | G | 2 | a0001c0001t0005 a0001c0001t0016 |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2361C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2361 | chr2 | 227556856 | ||||||
| chr2:227557045 | C | CT | 7 | a0001c0002t0002 a0001c0002t0024 a0001c0002t0028 others(4): Show |
69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2551dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2552 | INFO_REALIGN_3_PRIME | chr2 | 227557045 | |||||
| chr2:227557073 | G | A | 4 | a0001c0001t0041 a0001c0004t0006 a0001c0004t0009 others(1): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2578G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2578 | chr2 | 227557073 | ||||||
| chr2:227557176 | A | G | 1 | a0001c0003t0039 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2681A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2681 | chr2 | 227557176 | ||||||
| chr2:227557388 | C | T | 1 | a0001c0001t0038 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2893C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2893 | chr2 | 227557388 | ||||||
| chr2:227557535 | C | G | 4 | a0001c0003t0003 a0001c0003t0013 a0001c0003t0039 others(1): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3040C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3040 | chr2 | 227557535 | ||||||
| chr2:227557592 | GTTTA | G | 21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(18): Show |
170 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*3106_*3109delTTTA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3106 | INFO_REALIGN_3_PRIME | chr2 | 227557592 | |||||
| chr2:227557857 | A | T | 1 | a0001c0005t0014 | 2 | HG03453.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3362A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3362 | chr2 | 227557857 | ||||||
| chr2:227557905 | G | A | 2 | a0001c0001t0030 a0001c0001t0031 |
2 | HG03225.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3410G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3410 | chr2 | 227557905 | ||||||
| chr2:227557935 | T | C | 1 | a0001c0001t0026 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3440T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3440 | chr2 | 227557935 | ||||||
| chr2:227558386 | T | C | 6 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0018 others(3): Show |
19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3891T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3891 | chr2 | 227558386 | ||||||
| chr2:227558394 | G | T | 3 | a0001c0001t0011 a0001c0001t0026 a0001c0001t0033 |
5 | HG00639.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3899G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3899 | chr2 | 227558394 | ||||||
| chr2:227558394 | GT | G | 6 | a0001c0001t0041 a0001c0003t0003 a0001c0003t0039 others(3): Show |
48 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3910delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3910 | INFO_REALIGN_3_PRIME | chr2 | 227558394 | |||||
| chr2:227558426 | A | G | 3 | a0001c0001t0012 a0001c0001t0027 a0002c0007t0012 |
4 | HG02559.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3931A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3931 | chr2 | 227558426 | ||||||
| chr2:227558445 | G | C | 1 | a0001c0001t0015 | 2 | HG03471.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3950G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3950 | chr2 | 227558445 | ||||||
| chr2:227558572 | G | C | 4 | a0001c0001t0041 a0001c0004t0006 a0001c0004t0009 others(1): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4077G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4077 | chr2 | 227558572 | ||||||
| chr2:227558586 | G | A | 1 | a0001c0002t0035 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4091G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4091 | chr2 | 227558586 | ||||||
| chr2:227558677 | A | G | 2 | a0001c0001t0005 a0001c0001t0016 |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4182A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4182 | chr2 | 227558677 | ||||||
| chr2:227558973 | G | A | 19 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(16): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*4478G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4478 | chr2 | 227558973 | ||||||
| chr2:227559055 | C | G | 19 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(16): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*4560C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4560 | chr2 | 227559055 | ||||||
| chr2:227559062 | G | T | 1 | a0001c0001t0018 | 2 | HG02559.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4567G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4567 | chr2 | 227559062 | ||||||
| chr2:227559410 | G | A | 1 | a0001c0001t0015 | 2 | HG03471.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4915G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4915 | chr2 | 227559410 | ||||||
| chr2:227559499 | A | C | 1 | a0001c0001t0018 | 2 | HG02559.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5004A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5004 | chr2 | 227559499 | ||||||
| chr2:227559593 | C | T | 2 | a0001c0002t0007 a0001c0002t0035 |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5098C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5098 | chr2 | 227559593 | ||||||
| chr2:227559692 | C | T | 1 | a0001c0001t0005 | 15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5197C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5197 | chr2 | 227559692 | ||||||
| chr2:227559763 | C | G | 1 | a0001c0001t0015 | 2 | HG03471.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5268C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5268 | chr2 | 227559763 | ||||||
| chr2:227559894 | A | G | 1 | a0001c0001t0026 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5399A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5399 | chr2 | 227559894 | ||||||
| chr2:227559978 | G | A | 1 | a0001c0001t0015 | 2 | HG03471.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5483G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5483 | chr2 | 227559978 | ||||||
| chr2:227560008 | C | T | 1 | a0001c0001t0037 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5513C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5513 | chr2 | 227560008 | ||||||
| chr2:227560014 | C | T | 35 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(32): Show |
248 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*5519C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5519 | chr2 | 227560014 | ||||||
| chr2:227560238 | T | G | 1 | a0001c0002t0034 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5743T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5743 | chr2 | 227560238 | ||||||
| chr2:227560436 | C | CTAAT | 28 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(25): Show |
214 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*5942_*5943insAATT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5943 | INFO_REALIGN_3_PRIME | chr2 | 227560436 | |||||
| chr2:227560453 | T | C | 1 | a0001c0004t0009 | 6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5958T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5958 | chr2 | 227560453 | ||||||
| chr2:227560613 | A | T | 1 | a0001c0001t0032 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6118A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6118 | chr2 | 227560613 | ||||||
| chr2:227560711 | C | G | 4 | a0001c0003t0003 a0001c0003t0013 a0001c0003t0039 others(1): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*6216C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6216 | chr2 | 227560711 | ||||||
| chr2:227560723 | A | T | 4 | a0001c0003t0003 a0001c0003t0013 a0001c0003t0039 others(1): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*6228A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6228 | chr2 | 227560723 | ||||||
| chr2:227560741 | A | G | 4 | a0001c0003t0003 a0001c0003t0013 a0001c0003t0039 others(1): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*6246A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6246 | chr2 | 227560741 | ||||||
| chr2:227560746 | T | C | 1 | a0001c0001t0020 | 2 | HG02015.hp1 NA18985.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6251T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6251 | chr2 | 227560746 | ||||||
| chr2:227560817 | C | T | 2 | a0001c0001t0008 a0001c0001t0023 |
9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6322C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6322 | chr2 | 227560817 | ||||||
| chr2:227561074 | T | C | 1 | a0001c0001t0041 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6579T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6579 | chr2 | 227561074 | ||||||
| chr2:227561123 | T | C | 1 | a0001c0001t0030 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6628T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6628 | chr2 | 227561123 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227472605 | C | T | 14 | a0001c0001t0005g0003 a0001c0001t0005g0302 a0001c0001t0005g0303 others(11): Show |
16 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.167+17C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472605 | |||||||
| chr2:227472634 | T | C | 2 | a0001c0002t0002g0014 a0001c0002t0002g0015 |
2 | HG02071.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.167+46T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472634 | |||||||
| chr2:227472763 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(1): Show |
4 | HG00423.hp2 HG02071.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+175G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472763 | |||||||
| chr2:227472817 | T | C | 1 | a0001c0002t0002g0020 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.167+229T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472817 | |||||||
| chr2:227472872 | G | C | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.167+284G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472872 | |||||||
| chr2:227472903 | C | T | 65 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(62): Show |
69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.167+315C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472903 | |||||||
| chr2:227472942 | C | A | 19 | a0001c0004t0006g0004 a0001c0004t0006g0005 a0001c0004t0006g0038 others(16): Show |
21 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.167+354C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472942 | |||||||
| chr2:227472947 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.167+359C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472947 | |||||||
| chr2:227472958 | G | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.167+370G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472958 | |||||||
| chr2:227472988 | G | A | 1 | a0001c0001t0011g0094 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.167+400G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472988 | |||||||
| chr2:227473028 | A | G | 1 | a0001c0002t0002g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.167+440A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473028 | |||||||
| chr2:227473042 | C | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(243): Show |
256 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.167+454C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473042 | |||||||
| chr2:227473083 | G | A | 1 | a0001c0002t0002g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.167+495G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473083 | |||||||
| chr2:227473243 | G | T | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+655G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473243 | |||||||
| chr2:227473262 | G | C | 1 | a0001c0003t0003g0057 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.167+674G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473262 | |||||||
| chr2:227473273 | A | T | 1 | a0001c0002t0002g0298 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.167+685A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473273 | |||||||
| chr2:227473415 | C | T | 13 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(10): Show |
15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.167+827C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473415 | |||||||
| chr2:227473425 | C | T | 1 | a0001c0002t0002g0015 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.167+837C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473425 | |||||||
| chr2:227473491 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.167+903A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473491 | |||||||
| chr2:227473648 | C | T | 2 | a0001c0001t0027g0238 a0001c0001t0030g0239 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.167+1060C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473648 | |||||||
| chr2:227473768 | A | C | 1 | a0001c0001t0001g0237 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.167+1180A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473768 | |||||||
| chr2:227473792 | A | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.167+1204A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473792 | |||||||
| chr2:227473937 | G | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.167+1349G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473937 | |||||||
| chr2:227473937 | G | T | 1 | a0001c0001t0005g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.167+1349G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473937 | |||||||
| chr2:227473944 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.167+1356C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473944 | |||||||
| chr2:227474020 | A | G | 1 | a0001c0001t0017g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.167+1432A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474020 | |||||||
| chr2:227474026 | C | T | 1 | a0001c0001t0008g0037 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.167+1438C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474026 | |||||||
| chr2:227474188 | T | C | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.167+1600T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474188 | |||||||
| chr2:227474309 | C | G | 1 | a0001c0001t0005g0312 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.167+1721C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474309 | |||||||
| chr2:227474535 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.167+1947C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474535 | |||||||
| chr2:227474792 | T | C | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.167+2204T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474792 | |||||||
| chr2:227474921 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(175): Show |
185 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.167+2333A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474921 | |||||||
| chr2:227474925 | T | C | 1 | a0001c0001t0004g0095 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.167+2337T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474925 | |||||||
| chr2:227475051 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.167+2463A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475051 | |||||||
| chr2:227475165 | G | A | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.167+2577G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475165 | |||||||
| chr2:227475174 | T | C | 2 | a0001c0002t0002g0242 a0001c0002t0002g0243 |
2 | HG00408.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.167+2586T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475174 | |||||||
| chr2:227475322 | G | A | 1 | a0001c0004t0006g0038 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.167+2734G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475322 | |||||||
| chr2:227475346 | T | C | 1 | a0001c0001t0032g0096 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.167+2758T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475346 | |||||||
| chr2:227475806 | T | C | 1 | a0001c0001t0004g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.167+3218T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475806 | |||||||
| chr2:227475878 | T | C | 1 | a0001c0002t0002g0244 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.167+3290T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475878 | |||||||
| chr2:227475932 | A | G | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+3344A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475932 | |||||||
| chr2:227475998 | T | C | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+3410T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475998 | |||||||
| chr2:227476029 | G | T | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.167+3441G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476029 | |||||||
| chr2:227476067 | C | A | 9 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(6): Show |
9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.167+3479C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476067 | |||||||
| chr2:227476182 | G | A | 2 | a0001c0001t0008g0021 a0001c0001t0008g0022 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.167+3594G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476182 | |||||||
| chr2:227476227 | C | T | 4 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(1): Show |
4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+3639C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476227 | |||||||
| chr2:227476362 | A | G | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+3774A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476362 | |||||||
| chr2:227476544 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.167+3956C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476544 | |||||||
| chr2:227476750 | C | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.167+4162C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476750 | |||||||
| chr2:227476903 | CT | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(303): Show |
320 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.167+4331delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227476903 | ||||||
| chr2:227476996 | G | A | 1 | a0001c0001t0008g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.167+4408G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476996 | |||||||
| chr2:227477046 | C | T | 2 | a0001c0001t0005g0310 a0001c0001t0005g0311 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.167+4458C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227477046 | |||||||
| chr2:227477099 | G | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
158 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.167+4511G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227477099 | |||||||
| chr2:227477751 | A | G | 2 | a0001c0001t0016g0300 a0001c0001t0016g0301 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.167+5163A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227477751 | |||||||
| chr2:227477793 | A | G | 1 | a0001c0001t0025g0220 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.167+5205A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227477793 | |||||||
| chr2:227477962 | T | C | 4 | a0001c0003t0003g0057 a0001c0003t0003g0058 a0001c0003t0003g0059 others(1): Show |
4 | HG01952.hp2 HG01993.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+5374T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227477962 | |||||||
| chr2:227478046 | A | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.167+5458A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478046 | |||||||
| chr2:227478119 | T | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18971.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.167+5531T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478119 | |||||||
| chr2:227478125 | G | T | 5 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(2): Show |
5 | HG00621.hp2 NA18940.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.167+5537G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478125 | |||||||
| chr2:227478134 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0222 |
2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.167+5546G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478134 | |||||||
| chr2:227478139 | A | AT | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.167+5557dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227478139 | ||||||
| chr2:227478239 | T | TA | 152 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(149): Show |
157 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.167+5664dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227478239 | ||||||
| chr2:227478239 | T | TAA | 13 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(10): Show |
14 | HG00738.hp2 HG02055.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.167+5663_167+5664d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227478239 | ||||||
| chr2:227478239 | T | TAAA | 12 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0040 others(9): Show |
13 | HG02109.hp2 HG02129.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.167+5662_167+5664d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227478239 | ||||||
| chr2:227478251 | AATAC | A | 28 | a0001c0003t0003g0057 a0001c0003t0003g0058 a0001c0003t0003g0059 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.167+5670_167+5673d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227478251 | ||||||
| chr2:227478327 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.167+5739G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478327 | |||||||
| chr2:227478352 | T | C | 1 | a0001c0003t0003g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.167+5764T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478352 | |||||||
| chr2:227478409 | C | T | 1 | a0001c0002t0002g0297 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.167+5821C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478409 | |||||||
| chr2:227478632 | C | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.167+6044C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478632 | |||||||
| chr2:227478864 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.167+6276A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478864 | |||||||
| chr2:227478894 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.167+6306G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478894 | |||||||
| chr2:227478940 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.167+6352T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478940 | |||||||
| chr2:227479085 | A | G | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.167+6497A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479085 | |||||||
| chr2:227479326 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.167+6738T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479326 | |||||||
| chr2:227479444 | T | G | 66 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(63): Show |
70 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.167+6856T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479444 | |||||||
| chr2:227479510 | T | C | 1 | a0001c0001t0038g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.167+6922T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479510 | |||||||
| chr2:227479525 | AG | A | 3 | a0001c0001t0004g0117 a0001c0001t0004g0120 a0001c0001t0037g0118 |
3 | HG00738.hp1 HG00741.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.167+6938delG | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479525 | |||||||
| chr2:227479629 | C | T | 28 | a0001c0003t0003g0057 a0001c0003t0003g0058 a0001c0003t0003g0059 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.167+7041C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479629 | |||||||
| chr2:227479841 | A | T | 2 | a0001c0001t0016g0300 a0001c0001t0016g0301 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.167+7253A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479841 | |||||||
| chr2:227479904 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
165 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.167+7316T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479904 | |||||||
| chr2:227479952 | A | T | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.167+7364A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479952 | |||||||
| chr2:227480008 | A | G | 1 | a0001c0004t0006g0054 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.167+7420A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480008 | |||||||
| chr2:227480084 | G | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.167+7496G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480084 | |||||||
| chr2:227480237 | A | G | 1 | a0001c0002t0028g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.167+7649A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480237 | |||||||
| chr2:227480386 | C | T | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.167+7798C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480386 | |||||||
| chr2:227480394 | CTTATT | C | 4 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(1): Show |
4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+7824_167+7828d others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227480394 | ||||||
| chr2:227480591 | CT | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.167+8018delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227480591 | ||||||
| chr2:227480599 | T | C | 9 | a0001c0004t0006g0005 a0001c0004t0006g0038 a0001c0004t0006g0049 others(6): Show |
10 | HG00738.hp2 HG02129.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.167+8011T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480599 | |||||||
| chr2:227480692 | C | G | 4 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(1): Show |
4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+8104C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480692 | |||||||
| chr2:227480770 | G | A | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.167+8182G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480770 | |||||||
| chr2:227480867 | A | G | 10 | a0001c0002t0002g0013 a0001c0002t0002g0242 a0001c0002t0002g0243 others(7): Show |
11 | HG00408.hp2 HG00438.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.167+8279A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480867 | |||||||
| chr2:227481043 | G | T | 1 | a0001c0004t0009g0048 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.167+8455G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481043 | |||||||
| chr2:227481099 | CT | C | 73 | a0001c0001t0011g0094 a0001c0001t0011g0228 a0001c0001t0015g0235 others(70): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.167+8535delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | ||||||
| chr2:227481099 | CTT | C | 25 | a0001c0001t0001g0221 a0001c0001t0011g0226 a0001c0001t0017g0229 others(22): Show |
26 | HG00738.hp2 HG01952.hp2 HG02129.hp1 others(23): Show |
intron_variant | MODIFIER | c.167+8534_167+8535d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | ||||||
| chr2:227481099 | CTTT | C | 18 | a0001c0001t0001g0109 a0001c0001t0004g0095 a0001c0001t0004g0211 others(15): Show |
19 | HG02109.hp2 HG02273.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.167+8533_167+8535d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | ||||||
| chr2:227481099 | CTTTT | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
152 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.167+8532_167+8535d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | ||||||
| chr2:227481099 | CTTTTT | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0121 others(11): Show |
15 | HG00558.hp1 HG00558.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.167+8531_167+8535d others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | ||||||
| chr2:227481099 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.167+8526_167+8535d others(12): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | ||||||
| chr2:227481120 | TTTTG | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
7 | HG02074.hp2 NA18944.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.167+8533_167+8536d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481120 | |||||||
| chr2:227481259 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.167+8671T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481259 | |||||||
| chr2:227481326 | T | C | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.167+8738T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481326 | |||||||
| chr2:227481806 | T | C | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.167+9218T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481806 | |||||||
| chr2:227481863 | C | CT | 30 | a0001c0001t0001g0007 a0001c0001t0001g0109 a0001c0001t0001g0126 others(27): Show |
33 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.167+9297dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481863 | ||||||
| chr2:227481863 | CT | C | 24 | a0001c0001t0001g0011 a0001c0001t0001g0206 a0001c0001t0001g0207 others(21): Show |
25 | HG00639.hp1 HG01069.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.167+9297delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481863 | ||||||
| chr2:227481899 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.167+9311G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481899 | |||||||
| chr2:227481959 | G | A | 9 | a0001c0004t0006g0005 a0001c0004t0006g0038 a0001c0004t0006g0049 others(6): Show |
10 | HG00738.hp2 HG02129.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.167+9371G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481959 | |||||||
| chr2:227481959 | G | T | 1 | a0001c0002t0002g0270 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.167+9371G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481959 | |||||||
| chr2:227481966 | C | T | 1 | a0001c0001t0016g0301 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.167+9378C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481966 | |||||||
| chr2:227481985 | C | A | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.167+9397C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481985 | |||||||
| chr2:227482009 | G | A | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.167+9421G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482009 | |||||||
| chr2:227482011 | G | A | 2 | a0001c0002t0002g0246 a0001c0002t0002g0290 |
2 | NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.167+9423G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482011 | |||||||
| chr2:227482055 | C | T | 10 | a0001c0001t0005g0003 a0001c0001t0005g0302 a0001c0001t0005g0303 others(7): Show |
12 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.167+9467C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482055 | |||||||
| chr2:227482071 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(243): Show |
256 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.168-9476C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482071 | |||||||
| chr2:227482101 | G | A | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.168-9446G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482101 | |||||||
| chr2:227482232 | A | C | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(2): Show |
5 | NA18960.hp2 NA18975.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-9315A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482232 | |||||||
| chr2:227482293 | C | T | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168-9254C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482293 | |||||||
| chr2:227482370 | A | T | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168-9177A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482370 | |||||||
| chr2:227482407 | T | A | 2 | a0001c0001t0008g0021 a0001c0001t0008g0022 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.168-9140T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482407 | |||||||
| chr2:227482480 | T | C | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-9067T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482480 | |||||||
| chr2:227482498 | A | G | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168-9049A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482498 | |||||||
| chr2:227482534 | C | T | 6 | a0001c0004t0009g0043 a0001c0004t0009g0044 a0001c0004t0009g0045 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-9013C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482534 | |||||||
| chr2:227482577 | C | T | 3 | a0001c0002t0002g0284 a0001c0002t0002g0285 a0001c0002t0002g0286 |
3 | HG01106.hp1 HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.168-8970C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482577 | |||||||
| chr2:227482609 | G | A | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168-8938G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482609 | |||||||
| chr2:227482979 | CT | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(272): Show |
288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.168-8550delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227482979 | ||||||
| chr2:227482979 | CTT | C | 8 | a0001c0001t0001g0128 a0001c0002t0007g0006 a0001c0002t0007g0089 others(5): Show |
9 | HG01243.hp1 HG01255.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.168-8551_168-8550d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227482979 | ||||||
| chr2:227483178 | C | G | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-8369C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483178 | |||||||
| chr2:227483337 | C | T | 57 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(54): Show |
61 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-8210C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483337 | |||||||
| chr2:227483569 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.168-7978T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483569 | |||||||
| chr2:227483593 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.168-7954C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483593 | |||||||
| chr2:227483596 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.168-7951T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483596 | |||||||
| chr2:227483655 | A | G | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-7892A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483655 | |||||||
| chr2:227483766 | T | A | 2 | a0001c0004t0006g0005 a0001c0004t0006g0049 |
3 | HG00738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.168-7781T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483766 | |||||||
| chr2:227483789 | C | T | 4 | a0001c0004t0006g0004 a0001c0004t0006g0040 a0001c0004t0006g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-7758C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483789 | |||||||
| chr2:227483957 | T | G | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.168-7590T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483957 | |||||||
| chr2:227484257 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.168-7290C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484257 | |||||||
| chr2:227484406 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
219 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.168-7141C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484406 | |||||||
| chr2:227484570 | A | G | 1 | a0001c0002t0002g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.168-6977A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484570 | |||||||
| chr2:227484677 | GTTTTTTT others(7): Show |
G | 6 | a0001c0001t0008g0027 a0001c0001t0008g0037 a0001c0001t0018g0031 others(3): Show |
6 | HG01081.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-6859_168-6846d others(16): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | ||||||
| chr2:227484677 | GTTTTTTT others(8): Show |
G | 11 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(8): Show |
11 | HG00639.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.168-6859_168-6845d others(17): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | ||||||
| chr2:227484677 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0041g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168-6859_168-6843d others(19): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | ||||||
| chr2:227484677 | GTTTTTTT others(17): Show |
G | 1 | a0001c0003t0003g0081 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.168-6859_168-6836d others(26): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | ||||||
| chr2:227484677 | GTTTTTTT others(18): Show |
G | 35 | a0001c0001t0004g0198 a0001c0001t0017g0229 a0001c0003t0003g0055 others(32): Show |
35 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.168-6859_168-6835d others(27): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | ||||||
| chr2:227484677 | GTTTTTTT others(19): Show |
G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
175 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.168-6859_168-6834d others(28): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | ||||||
| chr2:227484677 | GTTTTTTT others(20): Show |
G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0237 |
2 | HG01884.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.168-6859_168-6833d others(29): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | ||||||
| chr2:227484686 | T | G | 1 | a0001c0002t0002g0257 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.168-6861T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484686 | |||||||
| chr2:227484688 | GT | G | 9 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0250 others(6): Show |
10 | HG02027.hp1 HG02602.hp1 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.168-6826delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484688 | ||||||
| chr2:227484688 | GTT | G | 23 | a0001c0002t0002g0002 a0001c0002t0002g0013 a0001c0002t0002g0244 others(20): Show |
24 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.168-6827_168-6826d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484688 | ||||||
| chr2:227484688 | GTTT | G | 28 | a0001c0002t0002g0012 a0001c0002t0002g0014 a0001c0002t0002g0015 others(25): Show |
28 | HG00408.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.168-6828_168-6826d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484688 | ||||||
| chr2:227484688 | GTTTTT | G | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-6830_168-6826d others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484688 | ||||||
| chr2:227484689 | T | G | 1 | a0001c0002t0002g0259 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.168-6858T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484689 | |||||||
| chr2:227484692 | T | G | 1 | a0001c0002t0002g0271 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.168-6855T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484692 | |||||||
| chr2:227484700 | T | G | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168-6847T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484700 | |||||||
| chr2:227484702 | T | G | 1 | a0001c0002t0002g0258 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.168-6845T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484702 | |||||||
| chr2:227484704 | T | G | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-6843T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484704 | |||||||
| chr2:227484705 | T | G | 5 | a0001c0002t0002g0275 a0001c0002t0002g0276 a0001c0002t0002g0284 others(2): Show |
5 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-6842T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484705 | |||||||
| chr2:227484715 | T | G | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-6832T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484715 | |||||||
| chr2:227485023 | T | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.168-6524T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485023 | |||||||
| chr2:227485053 | T | C | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168-6494T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485053 | |||||||
| chr2:227485061 | T | G | 1 | a0001c0004t0006g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.168-6486T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485061 | |||||||
| chr2:227485182 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG01081.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.168-6365A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485182 | |||||||
| chr2:227485243 | CT | C | 29 | a0001c0002t0002g0273 a0001c0003t0003g0055 a0001c0003t0003g0057 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-6285delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485243 | ||||||
| chr2:227485243 | CTT | C | 26 | a0001c0001t0001g0019 a0001c0001t0004g0192 a0001c0001t0005g0003 others(23): Show |
29 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.168-6286_168-6285d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485243 | ||||||
| chr2:227485243 | CTTT | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(185): Show |
195 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.168-6287_168-6285d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485243 | ||||||
| chr2:227485271 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.168-6276G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485271 | |||||||
| chr2:227485279 | C | T | 3 | a0001c0004t0009g0046 a0001c0004t0009g0047 a0001c0004t0009g0048 |
3 | HG02615.hp2 HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.168-6268C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485279 | |||||||
| chr2:227485297 | C | T | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0012g0188 others(3): Show |
6 | HG01081.hp1 HG01993.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-6250C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485297 | |||||||
| chr2:227485334 | T | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-6213T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485334 | |||||||
| chr2:227485403 | A | AT | 14 | a0001c0002t0002g0245 a0001c0002t0002g0248 a0001c0002t0002g0267 others(11): Show |
15 | HG00609.hp1 HG01243.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-6125dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485403 | ||||||
| chr2:227485403 | AT | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
175 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.168-6125delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485403 | ||||||
| chr2:227485403 | ATT | A | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG02257.hp2 HG02976.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-6126_168-6125d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485403 | ||||||
| chr2:227485428 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.168-6119A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485428 | |||||||
| chr2:227485643 | A | G | 3 | a0001c0001t0005g0003 a0001c0001t0005g0307 a0001c0001t0005g0308 |
5 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-5904A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485643 | |||||||
| chr2:227485680 | C | CTT | 247 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(244): Show |
257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.168-5866_168-5865i others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485680 | ||||||
| chr2:227485745 | T | C | 2 | a0001c0001t0016g0300 a0001c0001t0016g0301 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168-5802T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485745 | |||||||
| chr2:227485852 | C | T | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-5695C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485852 | |||||||
| chr2:227486067 | A | G | 8 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(5): Show |
9 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-5480A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486067 | |||||||
| chr2:227486116 | TAA | T | 15 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(12): Show |
15 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-5430_168-5429d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486116 | |||||||
| chr2:227486150 | C | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.168-5397C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486150 | |||||||
| chr2:227486256 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.168-5291T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486256 | |||||||
| chr2:227486291 | T | C | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-5256T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486291 | |||||||
| chr2:227486486 | G | A | 1 | a0001c0001t0041g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168-5061G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486486 | |||||||
| chr2:227486520 | A | G | 13 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(10): Show |
15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-5027A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486520 | |||||||
| chr2:227486545 | T | C | 5 | a0001c0001t0004g0134 a0001c0001t0004g0193 a0001c0001t0004g0198 others(2): Show |
5 | HG01071.hp2 HG01361.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-5002T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486545 | |||||||
| chr2:227486588 | ATATT | A | 10 | a0001c0001t0005g0003 a0001c0001t0005g0302 a0001c0001t0005g0303 others(7): Show |
12 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.168-4958_168-4955d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486588 | |||||||
| chr2:227486696 | T | C | 1 | a0001c0002t0002g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.168-4851T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486696 | |||||||
| chr2:227486717 | A | G | 1 | a0001c0001t0008g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.168-4830A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486717 | |||||||
| chr2:227487048 | G | A | 1 | a0001c0002t0036g0274 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.168-4499G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487048 | |||||||
| chr2:227487058 | A | G | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-4489A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487058 | |||||||
| chr2:227487295 | G | A | 2 | a0001c0001t0010g0033 a0001c0001t0010g0034 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.168-4252G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487295 | |||||||
| chr2:227487536 | C | G | 11 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(8): Show |
13 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.168-4011C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487536 | |||||||
| chr2:227487730 | C | T | 19 | a0001c0004t0006g0004 a0001c0004t0006g0005 a0001c0004t0006g0038 others(16): Show |
21 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.168-3817C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487730 | |||||||
| chr2:227487752 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.168-3795G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487752 | |||||||
| chr2:227488024 | T | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG00423.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.168-3523T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488024 | |||||||
| chr2:227488099 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0225 |
3 | HG03017.hp2 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.168-3448T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488099 | |||||||
| chr2:227488268 | G | A | 4 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(1): Show |
4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-3279G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488268 | |||||||
| chr2:227488355 | G | T | 69 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(66): Show |
70 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.168-3192G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488355 | |||||||
| chr2:227488405 | G | A | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168-3142G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488405 | |||||||
| chr2:227488454 | G | A | 1 | a0001c0002t0002g0250 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.168-3093G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488454 | |||||||
| chr2:227488495 | T | C | 1 | a0001c0002t0002g0278 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.168-3052T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488495 | |||||||
| chr2:227488595 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.168-2952G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488595 | |||||||
| chr2:227488599 | G | A | 1 | a0001c0004t0006g0005 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.168-2948G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488599 | |||||||
| chr2:227488948 | G | A | 19 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(16): Show |
19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.168-2599G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488948 | |||||||
| chr2:227489084 | G | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-2463G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489084 | |||||||
| chr2:227489110 | C | T | 6 | a0001c0004t0009g0043 a0001c0004t0009g0044 a0001c0004t0009g0045 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-2437C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489110 | |||||||
| chr2:227489215 | T | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.168-2332T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489215 | |||||||
| chr2:227489223 | G | GT | 27 | a0001c0001t0008g0023 a0001c0002t0002g0013 a0001c0002t0002g0242 others(24): Show |
29 | HG00408.hp2 HG00738.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.168-2299dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227489223 | ||||||
| chr2:227489223 | G | GTT | 9 | a0001c0001t0018g0031 a0001c0001t0018g0032 a0001c0002t0002g0266 others(6): Show |
10 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.168-2300_168-2299d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227489223 | ||||||
| chr2:227489223 | GT | G | 47 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0114 others(44): Show |
48 | HG00642.hp2 HG00741.hp2 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.168-2299delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227489223 | ||||||
| chr2:227489223 | GTT | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.168-2300_168-2299d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227489223 | ||||||
| chr2:227489291 | C | T | 8 | a0001c0001t0001g0221 a0001c0001t0032g0096 a0001c0004t0009g0043 others(5): Show |
8 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-2256C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489291 | |||||||
| chr2:227489437 | G | T | 19 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(16): Show |
19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.168-2110G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489437 | |||||||
| chr2:227489560 | T | G | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1987T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489560 | |||||||
| chr2:227489708 | C | T | 19 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(16): Show |
19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.168-1839C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489708 | |||||||
| chr2:227489726 | C | G | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-1821C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489726 | |||||||
| chr2:227489756 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.168-1791G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489756 | |||||||
| chr2:227489819 | C | CT | 41 | a0001c0001t0001g0240 a0001c0001t0004g0192 a0001c0001t0018g0032 others(38): Show |
42 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.168-1714dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227489819 | ||||||
| chr2:227489865 | G | T | 1 | a0001c0004t0006g0053 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.168-1682G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489865 | |||||||
| chr2:227489878 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(144): Show |
152 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.168-1669C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489878 | |||||||
| chr2:227489917 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.168-1630G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489917 | |||||||
| chr2:227489971 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.168-1576A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489971 | |||||||
| chr2:227490112 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(175): Show |
185 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.168-1435A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490112 | |||||||
| chr2:227490178 | A | C | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.168-1369A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490178 | |||||||
| chr2:227490360 | C | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.168-1187C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490360 | |||||||
| chr2:227490495 | G | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-1052G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490495 | |||||||
| chr2:227490577 | C | CA | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(146): Show |
154 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.168-953dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227490577 | ||||||
| chr2:227490577 | CA | C | 25 | a0001c0003t0003g0057 a0001c0003t0003g0058 a0001c0003t0003g0059 others(22): Show |
25 | HG00423.hp1 HG00609.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.168-953delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227490577 | ||||||
| chr2:227490702 | C | T | 5 | a0001c0001t0004g0134 a0001c0001t0004g0193 a0001c0001t0004g0198 others(2): Show |
5 | HG01071.hp2 HG01361.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-845C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490702 | |||||||
| chr2:227490816 | G | A | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168-731G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490816 | |||||||
| chr2:227490830 | A | T | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-717A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490830 | |||||||
| chr2:227490934 | C | T | 1 | a0001c0001t0004g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.168-613C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490934 | |||||||
| chr2:227490935 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0017g0229 a0001c0001t0017g0231 |
3 | HG03209.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.168-612G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490935 | |||||||
| chr2:227491055 | T | A | 2 | a0001c0005t0014g0029 a0001c0005t0014g0030 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.168-492T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491055 | |||||||
| chr2:227491161 | A | G | 2 | a0001c0001t0010g0033 a0001c0001t0010g0034 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.168-386A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491161 | |||||||
| chr2:227491432 | A | G | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-115A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491432 | |||||||
| chr2:227491442 | T | C | 1 | a0001c0003t0003g0081 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.168-105T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491442 | |||||||
| chr2:227491466 | GAAATATT others(1): Show |
G | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-80_168-73delAA others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491466 | |||||||
| chr2:227491498 | A | T | 1 | a0001c0003t0003g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.168-49A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491498 | |||||||
| chr2:227491648 | G | GT | 6 | a0001c0002t0002g0243 a0001c0002t0002g0264 a0001c0002t0002g0295 others(3): Show |
6 | HG00408.hp2 HG01243.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.261+23dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227491648 | ||||||
| chr2:227491648 | GT | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(218): Show |
230 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.261+23delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227491648 | ||||||
| chr2:227491898 | C | T | 2 | a0001c0005t0014g0029 a0001c0005t0014g0030 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.261+258C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227491898 | |||||||
| chr2:227492361 | G | A | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+721G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492361 | |||||||
| chr2:227492399 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(244): Show |
257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.261+759C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492399 | |||||||
| chr2:227492534 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.261+894A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492534 | |||||||
| chr2:227492663 | G | C | 2 | a0001c0001t0005g0310 a0001c0001t0005g0311 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.261+1023G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492663 | |||||||
| chr2:227492666 | A | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+1026A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492666 | |||||||
| chr2:227492986 | A | C | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.261+1346A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492986 | |||||||
| chr2:227493255 | G | C | 1 | a0002c0006t0002g0252 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.261+1615G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227493255 | |||||||
| chr2:227493327 | T | G | 19 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(16): Show |
19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.261+1687T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227493327 | |||||||
| chr2:227493725 | A | G | 19 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(16): Show |
19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.261+2085A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227493725 | |||||||
| chr2:227493943 | C | G | 6 | a0001c0002t0002g0012 a0001c0002t0002g0261 a0001c0002t0002g0262 others(3): Show |
7 | HG02083.hp1 HG02132.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.261+2303C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227493943 | |||||||
| chr2:227494001 | A | G | 1 | a0001c0002t0002g0242 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.261+2361A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494001 | |||||||
| chr2:227494037 | G | GTAAA | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+2399_261+2402d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227494037 | ||||||
| chr2:227494184 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.261+2544A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494184 | |||||||
| chr2:227494193 | C | T | 10 | a0001c0002t0022g0061 a0001c0004t0006g0005 a0001c0004t0006g0038 others(7): Show |
11 | HG00738.hp2 HG02129.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.261+2553C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494193 | |||||||
| chr2:227494194 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.261+2554G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494194 | |||||||
| chr2:227494245 | C | CGTGCAAG others(1): Show |
6 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0025 others(3): Show |
6 | HG00639.hp1 HG01081.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.261+2608_261+2615d others(10): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227494245 | ||||||
| chr2:227494365 | G | A | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+2725G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494365 | |||||||
| chr2:227494479 | C | A | 2 | a0001c0001t0019g0165 a0001c0001t0019g0199 |
2 | NA18989.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.261+2839C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494479 | |||||||
| chr2:227494574 | G | T | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+2934G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494574 | |||||||
| chr2:227494594 | A | T | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+2954A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494594 | |||||||
| chr2:227494699 | T | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02257.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.261+3059T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494699 | |||||||
| chr2:227495507 | C | T | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+3867C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495507 | |||||||
| chr2:227495533 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02132.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.261+3893G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495533 | |||||||
| chr2:227495545 | C | CA | 35 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0169 others(32): Show |
37 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.261+3924dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227495545 | ||||||
| chr2:227495545 | CA | C | 24 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(21): Show |
24 | HG00609.hp1 HG00639.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.261+3924delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227495545 | ||||||
| chr2:227495812 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0017g0229 a0001c0001t0017g0231 |
3 | HG03209.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.261+4172A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495812 | |||||||
| chr2:227495857 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(190): Show |
202 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.261+4217G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495857 | |||||||
| chr2:227495873 | C | G | 1 | a0001c0001t0032g0096 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.261+4233C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495873 | |||||||
| chr2:227495881 | T | A | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.261+4241T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495881 | |||||||
| chr2:227495913 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.261+4273G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495913 | |||||||
| chr2:227496033 | G | A | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.261+4393G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496033 | |||||||
| chr2:227496085 | C | T | 2 | a0001c0003t0003g0063 a0001c0003t0003g0071 |
2 | NA18947.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.261+4445C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496085 | |||||||
| chr2:227496093 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.261+4453A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496093 | |||||||
| chr2:227496121 | A | AAAAG | 193 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(190): Show |
202 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.261+4485_261+4488d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227496121 | ||||||
| chr2:227496129 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.261+4489A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496129 | |||||||
| chr2:227496436 | C | T | 9 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(6): Show |
9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+4796C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496436 | |||||||
| chr2:227496441 | C | CA | 243 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(240): Show |
253 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.261+4813dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227496441 | ||||||
| chr2:227496453 | A | T | 3 | a0001c0002t0002g0247 a0001c0002t0002g0270 a0001c0002t0002g0297 |
3 | NA18986.hp1 NA18999.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.261+4813A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496453 | |||||||
| chr2:227496454 | T | A | 283 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(280): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.261+4814T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496454 | |||||||
| chr2:227496675 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.261+5035A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496675 | |||||||
| chr2:227496703 | T | G | 1 | a0001c0002t0028g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.261+5063T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496703 | |||||||
| chr2:227496712 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | NA18943.hp2 NA19054.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.261+5072C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496712 | |||||||
| chr2:227496984 | A | T | 1 | a0001c0002t0002g0247 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.261+5344A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496984 | |||||||
| chr2:227496991 | C | T | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+5351C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496991 | |||||||
| chr2:227497080 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.261+5440G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497080 | |||||||
| chr2:227497165 | T | TC | 40 | a0001c0001t0001g0008 a0001c0001t0001g0128 a0001c0001t0001g0137 others(37): Show |
41 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.261+5533dupC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497165 | ||||||
| chr2:227497171 | C | A | 1 | a0001c0004t0006g0050 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.261+5531C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497171 | |||||||
| chr2:227497179 | A | C | 8 | a0001c0001t0001g0139 a0001c0002t0007g0006 a0001c0002t0007g0089 others(5): Show |
9 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+5539A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497179 | |||||||
| chr2:227497540 | A | T | 2 | a0001c0002t0002g0251 a0001c0002t0002g0268 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.261+5900A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497540 | |||||||
| chr2:227497574 | A | T | 1 | a0001c0001t0001g0139 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.261+5934A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497574 | |||||||
| chr2:227497601 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.261+5961T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497601 | |||||||
| chr2:227497613 | G | A | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.261+5973G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497613 | |||||||
| chr2:227497717 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0232 |
2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.261+6077G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497717 | |||||||
| chr2:227497719 | GTTTC | G | 4 | a0001c0001t0008g0021 a0001c0001t0008g0023 a0001c0001t0023g0024 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+6086_261+6089d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497719 | ||||||
| chr2:227497724 | TTTC | T | 3 | a0001c0001t0008g0022 a0001c0001t0008g0025 a0001c0001t0008g0027 |
3 | HG01081.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.261+6087_261+6089d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497724 | ||||||
| chr2:227497727 | C | CTTGTTT | 5 | a0001c0001t0005g0303 a0001c0001t0005g0304 a0001c0001t0005g0306 others(2): Show |
5 | HG02717.hp1 HG02970.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+6089_261+6094d others(8): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497727 | ||||||
| chr2:227497727 | C | G | 1 | a0001c0001t0008g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.261+6087C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497727 | |||||||
| chr2:227497728 | T | G | 1 | a0001c0001t0008g0037 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.261+6088T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497728 | |||||||
| chr2:227497729 | T | G | 3 | a0001c0001t0008g0022 a0001c0001t0008g0025 a0001c0001t0008g0027 |
3 | HG01081.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.261+6089T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497729 | |||||||
| chr2:227497730 | G | GTTTTTTT others(12): Show |
1 | a0001c0002t0002g0286 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.261+6094_261+6095i others(21): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497730 | ||||||
| chr2:227497730 | G | T | 5 | a0001c0001t0008g0022 a0001c0001t0008g0025 a0001c0001t0008g0026 others(2): Show |
5 | HG00639.hp1 HG01081.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.261+6090G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497730 | |||||||
| chr2:227497730 | GTTTTGTT others(4): Show |
G | 1 | a0001c0001t0021g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.261+6095_261+6105d others(13): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497730 | ||||||
| chr2:227497730 | GTTTTGTT others(6): Show |
G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+6095_261+6107d others(15): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497730 | ||||||
| chr2:227497730 | GTTTTGTT others(7): Show |
G | 2 | a0001c0004t0006g0040 a0001c0004t0042g0039 |
2 | HG02129.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.261+6095_261+6108d others(16): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497730 | ||||||
| chr2:227497731 | T | TTTTTG | 5 | a0001c0001t0005g0003 a0001c0001t0005g0302 a0001c0001t0005g0307 others(2): Show |
6 | HG00733.hp2 HG01069.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+6094_261+6095i others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497731 | ||||||
| chr2:227497731 | TTTTG | T | 28 | a0001c0002t0002g0012 a0001c0002t0002g0013 a0001c0002t0002g0015 others(25): Show |
30 | HG00408.hp2 HG00609.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.261+6095_261+6098d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497731 | ||||||
| chr2:227497732 | T | TTTTG | 4 | a0001c0001t0005g0087 a0001c0001t0005g0305 a0001c0001t0005g0310 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+6094_261+6095i others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497732 | ||||||
| chr2:227497732 | TTTG | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(128): Show |
136 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.261+6095_261+6097d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497732 | ||||||
| chr2:227497733 | TTG | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(52): Show |
55 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.261+6095_261+6096d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497733 | ||||||
| chr2:227497734 | TG | T | 11 | a0001c0001t0010g0036 a0001c0001t0011g0094 a0001c0001t0011g0228 others(8): Show |
11 | HG00639.hp2 HG01243.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.261+6095delG | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497734 | |||||||
| chr2:227497735 | G | T | 65 | a0001c0001t0001g0110 a0001c0001t0005g0003 a0001c0001t0005g0087 others(62): Show |
67 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.261+6095G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497735 | |||||||
| chr2:227497736 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.261+6096T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497736 | |||||||
| chr2:227497737 | T | G | 5 | a0001c0001t0011g0094 a0001c0001t0011g0228 a0001c0001t0017g0229 others(2): Show |
5 | HG00639.hp2 HG03209.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+6097T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497737 | |||||||
| chr2:227497738 | T | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(41): Show |
44 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.261+6098T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497738 | |||||||
| chr2:227497739 | T | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
111 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+6099T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497739 | |||||||
| chr2:227497761 | T | TTTTTG | 9 | a0001c0003t0003g0058 a0001c0003t0003g0062 a0001c0003t0003g0064 others(6): Show |
9 | HG00423.hp1 HG00609.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+6121_261+6122i others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497761 | |||||||
| chr2:227497761 | T | TTTTTTG | 13 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0066 others(10): Show |
13 | HG00099.hp1 HG01123.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.261+6121_261+6122i others(8): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497761 | |||||||
| chr2:227497761 | T | TTTTTTTT others(3): Show |
2 | a0001c0003t0013g0082 a0003c0008t0013g0080 |
2 | NA18943.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.261+6121_261+6122i others(12): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497761 | |||||||
| chr2:227497761 | T | TTTTTTTT others(4): Show |
1 | a0001c0003t0013g0072 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.261+6121_261+6122i others(13): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497761 | |||||||
| chr2:227497935 | G | A | 1 | a0001c0004t0042g0039 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.261+6295G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497935 | |||||||
| chr2:227498041 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.261+6401C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498041 | |||||||
| chr2:227498089 | A | C | 1 | a0001c0001t0001g0153 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.261+6449A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498089 | |||||||
| chr2:227498273 | T | C | 1 | a0001c0004t0009g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.261+6633T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498273 | |||||||
| chr2:227498548 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18971.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.261+6908A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498548 | |||||||
| chr2:227498576 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+6936A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498576 | |||||||
| chr2:227498598 | T | C | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.261+6958T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498598 | |||||||
| chr2:227498716 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.261+7076C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498716 | |||||||
| chr2:227499024 | GTAACAAA others(3): Show |
G | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.261+7385_261+7394d others(12): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499024 | |||||||
| chr2:227499461 | AAAACCCC others(9): Show |
A | 6 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(3): Show |
6 | HG00639.hp2 HG02647.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+7825_261+7840d others(18): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227499461 | ||||||
| chr2:227499468 | C | T | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+7828C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499468 | |||||||
| chr2:227499501 | G | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG01106.hp2 HG01123.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+7861G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499501 | |||||||
| chr2:227499639 | C | CA | 35 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(32): Show |
35 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.261+8013dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227499639 | ||||||
| chr2:227499639 | CA | C | 6 | a0001c0001t0016g0300 a0001c0001t0016g0301 a0001c0001t0018g0031 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+8013delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227499639 | ||||||
| chr2:227499697 | C | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+8057C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499697 | |||||||
| chr2:227499743 | A | G | 9 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(6): Show |
9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+8103A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499743 | |||||||
| chr2:227499769 | G | C | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+8129G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499769 | |||||||
| chr2:227500091 | G | A | 1 | a0001c0001t0001g0007 | 2 | NA18949.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.261+8451G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500091 | |||||||
| chr2:227500124 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.261+8484C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500124 | |||||||
| chr2:227500133 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.261+8493C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500133 | |||||||
| chr2:227500134 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.261+8494A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500134 | |||||||
| chr2:227500408 | G | T | 1 | a0001c0003t0003g0070 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.261+8768G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500408 | |||||||
| chr2:227500490 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.261+8850T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500490 | |||||||
| chr2:227500790 | A | T | 18 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(15): Show |
20 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.261+9150A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500790 | |||||||
| chr2:227500799 | AT | A | 9 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0025 others(6): Show |
9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+9169delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227500799 | ||||||
| chr2:227500800 | T | A | 52 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(49): Show |
54 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.261+9160T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500800 | |||||||
| chr2:227500915 | C | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0153 |
2 | NA18999.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.261+9275C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500915 | |||||||
| chr2:227500927 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0184 |
2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.261+9287G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500927 | |||||||
| chr2:227500950 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.261+9310G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500950 | |||||||
| chr2:227500953 | C | T | 13 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(10): Show |
15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.261+9313C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500953 | |||||||
| chr2:227501074 | G | A | 2 | a0001c0001t0001g0018 a0001c0003t0003g0075 |
2 | HG00609.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.261+9434G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501074 | |||||||
| chr2:227501083 | C | T | 1 | a0001c0001t0004g0179 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.261+9443C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501083 | |||||||
| chr2:227501107 | CAG | C | 4 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(1): Show |
4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+9470_261+9471d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227501107 | ||||||
| chr2:227501131 | G | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+9491G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501131 | |||||||
| chr2:227501273 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.261+9633G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501273 | |||||||
| chr2:227501414 | C | T | 4 | a0001c0004t0006g0004 a0001c0004t0006g0040 a0001c0004t0006g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+9774C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501414 | |||||||
| chr2:227501652 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG01256.hp2 HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.261+10012C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501652 | |||||||
| chr2:227501741 | G | A | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.261+10101G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501741 | |||||||
| chr2:227501770 | G | A | 2 | a0001c0001t0016g0300 a0001c0001t0016g0301 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.261+10130G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501770 | |||||||
| chr2:227501792 | C | T | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+10152C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501792 | |||||||
| chr2:227501885 | T | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(175): Show |
185 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.261+10245T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501885 | |||||||
| chr2:227501893 | CTG | C | 9 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(6): Show |
9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+10255_261+1025 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227501893 | ||||||
| chr2:227502006 | G | A | 1 | a0001c0004t0006g0049 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.261+10366G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502006 | |||||||
| chr2:227502012 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0217 |
3 | NA18940.hp2 NA19012.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.261+10372C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502012 | |||||||
| chr2:227502025 | A | G | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.261+10385A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502025 | |||||||
| chr2:227502069 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.261+10429A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502069 | |||||||
| chr2:227502514 | A | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(244): Show |
257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.261+10874A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502514 | |||||||
| chr2:227502655 | C | T | 17 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(14): Show |
19 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.261+11015C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502655 | |||||||
| chr2:227502865 | A | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+11225A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502865 | |||||||
| chr2:227502870 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.261+11230A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502870 | |||||||
| chr2:227502872 | A | G | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.261+11232A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502872 | |||||||
| chr2:227502931 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.261+11291T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502931 | |||||||
| chr2:227502985 | C | T | 2 | a0001c0005t0014g0029 a0001c0005t0014g0030 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.261+11345C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502985 | |||||||
| chr2:227503174 | T | A | 2 | a0001c0001t0021g0233 a0001c0001t0021g0234 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.261+11534T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503174 | |||||||
| chr2:227503201 | A | C | 1 | a0001c0002t0002g0015 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.261+11561A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503201 | |||||||
| chr2:227503239 | TA | T | 39 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(36): Show |
41 | HG00639.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.261+11615delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227503239 | ||||||
| chr2:227503501 | A | G | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+11861A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503501 | |||||||
| chr2:227503604 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.261+11964G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503604 | |||||||
| chr2:227503606 | G | A | 1 | a0001c0003t0003g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.261+11966G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503606 | |||||||
| chr2:227503650 | A | G | 1 | a0001c0001t0025g0220 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.261+12010A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503650 | |||||||
| chr2:227503687 | G | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+12047G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503687 | |||||||
| chr2:227503806 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.261+12166A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503806 | |||||||
| chr2:227503873 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.261+12233A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503873 | |||||||
| chr2:227504188 | A | AT | 22 | a0001c0001t0001g0101 a0001c0001t0001g0160 a0001c0001t0005g0003 others(19): Show |
25 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.261+12566dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227504188 | ||||||
| chr2:227504188 | A | G | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0012g0188 others(3): Show |
6 | HG01081.hp1 HG01993.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+12548A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504188 | |||||||
| chr2:227504188 | AT | A | 6 | a0001c0001t0001g0121 a0001c0001t0001g0156 a0001c0001t0001g0170 others(3): Show |
6 | HG00558.hp2 HG00733.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+12566delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227504188 | ||||||
| chr2:227504300 | C | G | 5 | a0001c0003t0003g0063 a0001c0003t0003g0071 a0001c0003t0013g0072 others(2): Show |
5 | NA18943.hp1 NA18944.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+12660C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504300 | |||||||
| chr2:227504359 | A | T | 2 | a0001c0005t0014g0029 a0001c0005t0014g0030 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.261+12719A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504359 | |||||||
| chr2:227504475 | G | A | 3 | a0001c0001t0005g0003 a0001c0001t0005g0307 a0001c0001t0005g0308 |
5 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+12835G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504475 | |||||||
| chr2:227504494 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.261+12854A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504494 | |||||||
| chr2:227504620 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.261+12980C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504620 | |||||||
| chr2:227504621 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.261+12981A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504621 | |||||||
| chr2:227504652 | A | G | 1 | a0001c0002t0002g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.261+13012A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504652 | |||||||
| chr2:227504747 | C | G | 1 | a0001c0002t0002g0259 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.261+13107C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504747 | |||||||
| chr2:227504889 | G | A | 1 | a0001c0001t0041g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.261+13249G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504889 | |||||||
| chr2:227504955 | T | C | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+13315T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504955 | |||||||
| chr2:227505207 | T | TTATCTC | 111 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
113 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.261+13567_261+1356 others(10): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505207 | |||||||
| chr2:227505460 | GGCATTTT others(11): Show |
G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+13824_261+1384 others(22): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227505460 | ||||||
| chr2:227505490 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.261+13850A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505490 | |||||||
| chr2:227505708 | T | C | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.261+14068T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505708 | |||||||
| chr2:227505711 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(175): Show |
185 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.261+14071G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505711 | |||||||
| chr2:227505782 | A | G | 3 | a0001c0001t0011g0226 a0001c0001t0026g0227 a0001c0001t0033g0178 |
3 | HG02647.hp1 HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.261+14142A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505782 | |||||||
| chr2:227505886 | C | T | 1 | a0001c0001t0008g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.262-14062C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505886 | |||||||
| chr2:227505887 | G | A | 2 | a0001c0001t0005g0310 a0001c0001t0005g0311 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.262-14061G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505887 | |||||||
| chr2:227506058 | A | T | 2 | a0001c0002t0002g0277 a0001c0002t0002g0287 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.262-13890A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506058 | |||||||
| chr2:227506183 | T | C | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-13765T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506183 | |||||||
| chr2:227506249 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.262-13699T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506249 | |||||||
| chr2:227506333 | A | T | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-13615A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506333 | |||||||
| chr2:227506378 | G | A | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.262-13570G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506378 | |||||||
| chr2:227506466 | C | T | 1 | a0001c0002t0002g0258 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.262-13482C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506466 | |||||||
| chr2:227506477 | C | G | 1 | a0001c0003t0003g0070 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.262-13471C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506477 | |||||||
| chr2:227506482 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.262-13466A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506482 | |||||||
| chr2:227506536 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.262-13412A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506536 | |||||||
| chr2:227506558 | T | TA | 31 | a0001c0001t0005g0309 a0001c0001t0016g0300 a0001c0001t0016g0301 others(28): Show |
33 | HG00738.hp2 HG01106.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.262-13369dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227506558 | ||||||
| chr2:227506558 | T | TAA | 8 | a0001c0001t0001g0171 a0001c0001t0001g0206 a0001c0001t0017g0229 others(5): Show |
8 | HG00438.hp1 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.262-13370_262-1336 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227506558 | ||||||
| chr2:227506558 | T | TAAA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(103): Show |
110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.262-13371_262-1336 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227506558 | ||||||
| chr2:227506558 | T | TAAAA | 42 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0111 others(39): Show |
43 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.262-13372_262-1336 others(8): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227506558 | ||||||
| chr2:227506558 | TA | T | 12 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(9): Show |
12 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.262-13369delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227506558 | ||||||
| chr2:227506630 | G | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-13318G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506630 | |||||||
| chr2:227506639 | G | A | 1 | a0001c0002t0002g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.262-13309G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506639 | |||||||
| chr2:227506984 | G | A | 1 | a0001c0001t0004g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.262-12964G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506984 | |||||||
| chr2:227507001 | A | G | 111 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
113 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.262-12947A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507001 | |||||||
| chr2:227507059 | A | G | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-12889A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507059 | |||||||
| chr2:227507076 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(150): Show |
158 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.262-12872A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507076 | |||||||
| chr2:227507183 | T | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0159 |
2 | HG01256.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.262-12765T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507183 | |||||||
| chr2:227507323 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.262-12625A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507323 | |||||||
| chr2:227507462 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.262-12486G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507462 | |||||||
| chr2:227507463 | C | T | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.262-12485C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507463 | |||||||
| chr2:227507560 | G | A | 1 | a0001c0002t0002g0248 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.262-12388G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507560 | |||||||
| chr2:227507589 | C | T | 1 | a0001c0004t0006g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.262-12359C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507589 | |||||||
| chr2:227507590 | G | A | 9 | a0001c0001t0005g0003 a0001c0001t0005g0302 a0001c0001t0005g0303 others(6): Show |
11 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.262-12358G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507590 | |||||||
| chr2:227507602 | C | CA | 112 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(109): Show |
119 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.262-12322dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | ||||||
| chr2:227507602 | C | CAA | 51 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0018 others(48): Show |
51 | HG00621.hp1 HG00642.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.262-12323_262-1232 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | ||||||
| chr2:227507602 | C | CAAA | 9 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0174 others(6): Show |
9 | HG00423.hp2 HG00639.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-12324_262-1232 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | ||||||
| chr2:227507602 | C | CAAAAAA | 21 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(18): Show |
21 | HG00099.hp1 HG01123.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.262-12327_262-1232 others(10): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | ||||||
| chr2:227507602 | C | CAAAAAAA | 7 | a0001c0003t0003g0063 a0001c0003t0003g0064 a0001c0003t0003g0066 others(4): Show |
7 | HG00423.hp1 HG00609.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-12328_262-1232 others(11): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | ||||||
| chr2:227507602 | CA | C | 14 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0102 others(11): Show |
14 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.262-12322delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | ||||||
| chr2:227507602 | CAAAAAAA others(1): Show |
C | 18 | a0001c0004t0006g0004 a0001c0004t0006g0005 a0001c0004t0006g0038 others(15): Show |
20 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.262-12329_262-1232 others(12): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | ||||||
| chr2:227507657 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.262-12291A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507657 | |||||||
| chr2:227507760 | G | GC | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-12187dupC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507760 | ||||||
| chr2:227507870 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.262-12078A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507870 | |||||||
| chr2:227508002 | CT | C | 46 | a0001c0001t0001g0115 a0001c0002t0002g0002 a0001c0002t0002g0020 others(43): Show |
48 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.262-11933delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227508002 | ||||||
| chr2:227508175 | A | G | 1 | a0001c0001t0041g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.262-11773A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508175 | |||||||
| chr2:227508192 | C | G | 2 | a0001c0005t0014g0029 a0001c0005t0014g0030 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.262-11756C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508192 | |||||||
| chr2:227508240 | T | C | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.262-11708T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508240 | |||||||
| chr2:227508339 | T | A | 2 | a0001c0001t0023g0024 a0001c0001t0023g0028 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.262-11609T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508339 | |||||||
| chr2:227508353 | A | T | 2 | a0001c0004t0006g0005 a0001c0004t0006g0049 |
3 | HG00738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.262-11595A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508353 | |||||||
| chr2:227508551 | G | A | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.262-11397G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508551 | |||||||
| chr2:227508688 | A | AT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(140): Show |
148 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.262-11247dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227508688 | ||||||
| chr2:227508899 | C | T | 65 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(62): Show |
69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.262-11049C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508899 | |||||||
| chr2:227508967 | G | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(144): Show |
152 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.262-10981G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508967 | |||||||
| chr2:227509254 | T | G | 17 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(14): Show |
17 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-10694T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509254 | |||||||
| chr2:227509528 | A | C | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-10420A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509528 | |||||||
| chr2:227509530 | G | T | 1 | a0001c0002t0002g0251 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.262-10418G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509530 | |||||||
| chr2:227509619 | A | G | 4 | a0001c0002t0002g0020 a0001c0002t0002g0256 a0001c0002t0002g0264 others(1): Show |
4 | NA18975.hp1 NA18980.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-10329A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509619 | |||||||
| chr2:227509812 | A | C | 9 | a0001c0004t0006g0005 a0001c0004t0006g0038 a0001c0004t0006g0049 others(6): Show |
10 | HG00738.hp2 HG02129.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-10136A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509812 | |||||||
| chr2:227509973 | C | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.262-9975C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509973 | |||||||
| chr2:227510051 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.262-9897T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510051 | |||||||
| chr2:227510071 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.262-9877A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510071 | |||||||
| chr2:227510269 | C | T | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.262-9679C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510269 | |||||||
| chr2:227510311 | C | T | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-9637C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510311 | |||||||
| chr2:227510366 | G | T | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-9582G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510366 | |||||||
| chr2:227510532 | GGAGGGGT | G | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-9412_262-9406d others(9): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227510532 | ||||||
| chr2:227510791 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.262-9157G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510791 | |||||||
| chr2:227510923 | TC | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0107 |
3 | HG02572.hp1 HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.262-9024delC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510923 | |||||||
| chr2:227511067 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.262-8881A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511067 | |||||||
| chr2:227511261 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.262-8687A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511261 | |||||||
| chr2:227511322 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(175): Show |
185 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.262-8626T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511322 | |||||||
| chr2:227511496 | C | T | 1 | a0001c0002t0002g0278 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.262-8452C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511496 | |||||||
| chr2:227511640 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.262-8308A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511640 | |||||||
| chr2:227511865 | A | G | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-8083A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511865 | |||||||
| chr2:227512028 | T | C | 1 | a0001c0001t0008g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.262-7920T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512028 | |||||||
| chr2:227512166 | A | G | 1 | a0001c0003t0003g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.262-7782A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512166 | |||||||
| chr2:227512239 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18971.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.262-7709C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512239 | |||||||
| chr2:227512382 | A | G | 3 | a0001c0001t0005g0003 a0001c0001t0005g0307 a0001c0001t0005g0308 |
5 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-7566A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512382 | |||||||
| chr2:227512403 | C | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
219 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.262-7545C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512403 | |||||||
| chr2:227512573 | C | T | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-7375C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512573 | |||||||
| chr2:227512578 | A | G | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(2): Show |
5 | NA18960.hp2 NA18975.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-7370A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512578 | |||||||
| chr2:227512615 | T | C | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-7333T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512615 | |||||||
| chr2:227512632 | G | T | 2 | a0001c0002t0002g0248 a0001c0002t0002g0267 |
2 | NA18948.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.262-7316G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512632 | |||||||
| chr2:227513004 | C | T | 2 | a0001c0004t0006g0005 a0001c0004t0006g0049 |
3 | HG00738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.262-6944C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513004 | |||||||
| chr2:227513034 | T | C | 2 | a0001c0001t0016g0300 a0001c0001t0016g0301 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.262-6914T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513034 | |||||||
| chr2:227513197 | G | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.262-6751G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513197 | |||||||
| chr2:227513236 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 |
4 | HG00733.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-6712A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513236 | |||||||
| chr2:227513357 | G | A | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-6591G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513357 | |||||||
| chr2:227513521 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.262-6427C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513521 | |||||||
| chr2:227513556 | A | G | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-6392A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513556 | |||||||
| chr2:227513651 | T | A | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.262-6297T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513651 | |||||||
| chr2:227513829 | T | C | 17 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(14): Show |
17 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-6119T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513829 | |||||||
| chr2:227513986 | G | A | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.262-5962G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513986 | |||||||
| chr2:227514142 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.262-5806T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514142 | |||||||
| chr2:227514145 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
133 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.262-5803C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514145 | |||||||
| chr2:227514304 | C | T | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.262-5644C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514304 | |||||||
| chr2:227514426 | C | T | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.262-5522C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514426 | |||||||
| chr2:227514506 | T | G | 1 | a0001c0001t0019g0199 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.262-5442T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514506 | |||||||
| chr2:227514578 | T | C | 2 | a0001c0001t0005g0087 a0001c0001t0005g0305 |
2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.262-5370T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514578 | |||||||
| chr2:227514683 | C | G | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-5265C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514683 | |||||||
| chr2:227514784 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.262-5164A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514784 | |||||||
| chr2:227515005 | C | T | 1 | a0001c0001t0004g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.262-4943C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515005 | |||||||
| chr2:227515021 | C | T | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-4927C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515021 | |||||||
| chr2:227515160 | A | G | 1 | a0001c0002t0002g0261 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.262-4788A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515160 | |||||||
| chr2:227515178 | C | T | 2 | a0001c0001t0005g0310 a0001c0001t0005g0311 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.262-4770C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515178 | |||||||
| chr2:227515341 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.262-4607A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515341 | |||||||
| chr2:227515489 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.262-4459A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515489 | |||||||
| chr2:227515585 | T | G | 1 | a0001c0002t0028g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.262-4363T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515585 | |||||||
| chr2:227515732 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(237): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.262-4216T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515732 | |||||||
| chr2:227515966 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.262-3982C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515966 | |||||||
| chr2:227516087 | T | C | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.262-3861T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516087 | |||||||
| chr2:227516304 | A | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.262-3644A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516304 | |||||||
| chr2:227516317 | T | C | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-3631T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516317 | |||||||
| chr2:227516378 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0017g0229 a0001c0001t0017g0231 |
3 | HG03209.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.262-3570A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516378 | |||||||
| chr2:227516392 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
219 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.262-3556T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516392 | |||||||
| chr2:227516727 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.262-3221C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516727 | |||||||
| chr2:227516860 | G | C | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.262-3088G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516860 | |||||||
| chr2:227517134 | C | G | 2 | a0001c0002t0002g0251 a0001c0002t0002g0268 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.262-2814C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517134 | |||||||
| chr2:227517147 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.262-2801A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517147 | |||||||
| chr2:227517306 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(174): Show |
184 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.262-2642A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517306 | |||||||
| chr2:227517453 | G | A | 1 | a0001c0001t0019g0165 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.262-2495G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517453 | |||||||
| chr2:227517482 | T | A | 1 | a0001c0002t0002g0281 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.262-2466T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517482 | |||||||
| chr2:227517491 | C | T | 1 | a0001c0001t0033g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.262-2457C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517491 | |||||||
| chr2:227517512 | C | T | 1 | a0001c0001t0010g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.262-2436C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517512 | |||||||
| chr2:227517550 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.262-2398G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517550 | |||||||
| chr2:227517574 | A | G | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.262-2374A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517574 | |||||||
| chr2:227517632 | C | T | 1 | a0001c0001t0018g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.262-2316C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517632 | |||||||
| chr2:227517637 | A | G | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | NA18943.hp2 NA19054.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.262-2311A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517637 | |||||||
| chr2:227517696 | C | G | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-2252C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517696 | |||||||
| chr2:227517768 | C | T | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.262-2180C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517768 | |||||||
| chr2:227518064 | G | A | 2 | a0001c0001t0005g0306 a0001c0001t0005g0312 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.262-1884G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518064 | |||||||
| chr2:227518207 | A | G | 1 | a0001c0002t0007g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.262-1741A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518207 | |||||||
| chr2:227518255 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.262-1693C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518255 | |||||||
| chr2:227518287 | G | A | 2 | a0001c0001t0004g0095 a0001c0001t0038g0116 |
2 | HG03491.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.262-1661G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518287 | |||||||
| chr2:227518306 | A | G | 1 | a0001c0001t0008g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.262-1642A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518306 | |||||||
| chr2:227518413 | GAATTCCG others(602): Show |
G | 1 | a0001c0001t0001g0139 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.262-1530_262-922de others(1): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227518413 | ||||||
| chr2:227518469 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(235): Show |
247 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.262-1479G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518469 | |||||||
| chr2:227518482 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.262-1466G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518482 | |||||||
| chr2:227518516 | C | CT | 25 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0114 others(22): Show |
25 | HG00558.hp2 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.262-1409dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227518516 | ||||||
| chr2:227518516 | C | CTT | 10 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0025 others(7): Show |
10 | HG00639.hp1 HG00639.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.262-1410_262-1409d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227518516 | ||||||
| chr2:227518516 | CT | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0105 others(30): Show |
34 | HG00423.hp1 HG00597.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.262-1409delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227518516 | ||||||
| chr2:227518528 | T | C | 1 | a0001c0001t0038g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.262-1420T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518528 | |||||||
| chr2:227518540 | A | C | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-1408A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518540 | |||||||
| chr2:227518544 | A | G | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.262-1404A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518544 | |||||||
| chr2:227518604 | A | G | 1 | a0001c0001t0004g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.262-1344A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518604 | |||||||
| chr2:227518609 | C | T | 2 | a0001c0001t0005g0310 a0001c0001t0005g0311 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.262-1339C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518609 | |||||||
| chr2:227518642 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.262-1306G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518642 | |||||||
| chr2:227518681 | G | A | 25 | a0001c0001t0001g0011 a0001c0001t0001g0114 a0001c0001t0001g0127 others(22): Show |
26 | HG00438.hp1 HG00597.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.262-1267G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518681 | |||||||
| chr2:227518746 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.262-1202G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518746 | |||||||
| chr2:227518782 | C | T | 65 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(62): Show |
69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.262-1166C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518782 | |||||||
| chr2:227518843 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.262-1105T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518843 | |||||||
| chr2:227518874 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(150): Show |
158 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.262-1074C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518874 | |||||||
| chr2:227518875 | G | A | 2 | a0001c0005t0014g0029 a0001c0005t0014g0030 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.262-1073G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518875 | |||||||
| chr2:227519172 | A | G | 2 | a0001c0002t0002g0275 a0001c0002t0002g0276 |
2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.262-776A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227519172 | |||||||
| chr2:227519189 | T | G | 10 | a0001c0002t0002g0249 a0001c0002t0002g0254 a0001c0002t0002g0258 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-759T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227519189 | |||||||
| chr2:227519239 | T | C | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-709T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227519239 | |||||||
| chr2:227519317 | T | C | 2 | a0001c0003t0003g0065 a0001c0003t0003g0076 |
2 | HG00423.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.262-631T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227519317 | |||||||
| chr2:227519598 | T | C | 1 | a0001c0003t0013g0072 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.262-350T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227519598 | |||||||
| chr2:227519684 | GCCAAGAC others(10): Show |
G | 2 | a0001c0001t0005g0087 a0001c0001t0005g0305 |
2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.262-260_262-244del others(17): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227519684 | ||||||
| chr2:227520207 | T | C | 1 | a0001c0002t0002g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.377+144T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520207 | |||||||
| chr2:227520288 | AC | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.377+227delC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 227520288 | ||||||
| chr2:227520366 | G | A | 1 | a0001c0004t0006g0053 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.377+303G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520366 | |||||||
| chr2:227520678 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.377+615A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520678 | |||||||
| chr2:227520801 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.377+738T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520801 | |||||||
| chr2:227520915 | A | G | 1 | a0001c0002t0002g0254 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.377+852A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520915 | |||||||
| chr2:227520917 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.377+854G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520917 | |||||||
| chr2:227521071 | CT | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
219 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.377+1018delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 227521071 | ||||||
| chr2:227521129 | G | A | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.377+1066G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521129 | |||||||
| chr2:227521188 | C | G | 25 | a0001c0001t0001g0011 a0001c0001t0001g0114 a0001c0001t0001g0127 others(22): Show |
26 | HG00438.hp1 HG00597.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.377+1125C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521188 | |||||||
| chr2:227521340 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.377+1277T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521340 | |||||||
| chr2:227521512 | A | G | 1 | a0001c0002t0002g0283 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.377+1449A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521512 | |||||||
| chr2:227521587 | C | G | 1 | a0001c0001t0017g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.377+1524C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521587 | |||||||
| chr2:227521769 | T | C | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.377+1706T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521769 | |||||||
| chr2:227521825 | CA | C | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.377+1765delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 227521825 | ||||||
| chr2:227521908 | T | C | 19 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(16): Show |
19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.377+1845T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521908 | |||||||
| chr2:227521926 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.378-1837G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521926 | |||||||
| chr2:227522109 | T | C | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.378-1654T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227522109 | |||||||
| chr2:227522224 | A | G | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.378-1539A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227522224 | |||||||
| chr2:227522473 | A | T | 1 | a0001c0001t0004g0117 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.378-1290A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227522473 | |||||||
| chr2:227522482 | G | A | 9 | a0001c0001t0005g0003 a0001c0001t0005g0302 a0001c0001t0005g0303 others(6): Show |
11 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.378-1281G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227522482 | |||||||
| chr2:227522649 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.378-1114A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227522649 | |||||||
| chr2:227523074 | C | T | 1 | a0001c0001t0004g0179 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.378-689C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523074 | |||||||
| chr2:227523075 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.378-688A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523075 | |||||||
| chr2:227523083 | A | G | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.378-680A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523083 | |||||||
| chr2:227523601 | C | T | 1 | a0001c0001t0040g0142 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.378-162C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523601 | |||||||
| chr2:227523678 | G | C | 1 | a0001c0001t0012g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.378-85G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523678 | |||||||
| chr2:227523742 | A | G | 1 | a0001c0001t0004g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.378-21A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523742 | |||||||
| chr2:227524079 | G | T | 9 | a0001c0001t0005g0003 a0001c0001t0005g0302 a0001c0001t0005g0303 others(6): Show |
11 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.540+154G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524079 | |||||||
| chr2:227524105 | T | C | 2 | a0001c0001t0021g0233 a0001c0001t0021g0234 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.540+180T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524105 | |||||||
| chr2:227524155 | GGTGAGTT | G | 6 | a0001c0004t0009g0043 a0001c0004t0009g0044 a0001c0004t0009g0045 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+231_540+237del others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524155 | |||||||
| chr2:227524163 | A | C | 6 | a0001c0004t0009g0043 a0001c0004t0009g0044 a0001c0004t0009g0045 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+238A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524163 | |||||||
| chr2:227524164 | T | A | 6 | a0001c0004t0009g0043 a0001c0004t0009g0044 a0001c0004t0009g0045 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+239T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524164 | |||||||
| chr2:227524292 | AC | A | 22 | a0001c0001t0041g0086 a0001c0003t0003g0065 a0001c0003t0003g0076 others(19): Show |
24 | HG00423.hp1 HG00738.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.540+368delC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524292 | |||||||
| chr2:227524388 | A | C | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.541-374A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524388 | |||||||
| chr2:227524963 | C | G | 1 | a0001c0001t0016g0301 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.694+48C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227524963 | |||||||
| chr2:227524988 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.694+73A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227524988 | |||||||
| chr2:227525095 | A | ATTATATT others(2106): Show |
2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18971.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.694+347_694+348ins others(2113): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227525095 | ||||||
| chr2:227525263 | G | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(209): Show |
221 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.694+348G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525263 | |||||||
| chr2:227525370 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(175): Show |
185 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.694+455T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525370 | |||||||
| chr2:227525470 | A | G | 1 | a0001c0001t0026g0227 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.694+555A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525470 | |||||||
| chr2:227525474 | G | A | 9 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(6): Show |
9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+559G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525474 | |||||||
| chr2:227525544 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(236): Show |
248 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.694+629G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525544 | |||||||
| chr2:227525800 | C | G | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.694+885C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525800 | |||||||
| chr2:227525969 | T | G | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.694+1054T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525969 | |||||||
| chr2:227525987 | T | C | 22 | a0001c0001t0041g0086 a0001c0003t0003g0065 a0001c0003t0003g0076 others(19): Show |
24 | HG00423.hp1 HG00738.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.694+1072T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525987 | |||||||
| chr2:227526286 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
187 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.694+1371T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526286 | |||||||
| chr2:227526360 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.694+1445T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526360 | |||||||
| chr2:227526406 | T | TTTTTTAT others(318): Show |
11 | a0001c0003t0003g0065 a0001c0003t0003g0076 a0001c0004t0006g0005 others(8): Show |
12 | HG00423.hp1 HG00738.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.694+1501_694+1502i others(327): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | ||||||
| chr2:227526406 | T | TTTTTTAT others(321): Show |
2 | a0001c0004t0009g0044 a0001c0004t0009g0048 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.694+1501_694+1502i others(330): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | ||||||
| chr2:227526406 | T | TTTTTTAT others(319): Show |
1 | a0001c0001t0041g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.694+1501_694+1502i others(328): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | ||||||
| chr2:227526406 | T | TTTTTTAT others(318): Show |
3 | a0001c0004t0006g0004 a0001c0004t0006g0040 a0001c0004t0006g0041 |
4 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+1501_694+1502i others(327): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | ||||||
| chr2:227526406 | T | TTTTTTAT others(319): Show |
1 | a0001c0004t0006g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.694+1501_694+1502i others(328): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | ||||||
| chr2:227526406 | T | TTTTTTAT others(321): Show |
4 | a0001c0004t0009g0043 a0001c0004t0009g0045 a0001c0004t0009g0046 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+1501_694+1502i others(330): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | ||||||
| chr2:227526485 | A | G | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.694+1570A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526485 | |||||||
| chr2:227526518 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.694+1603A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526518 | |||||||
| chr2:227526539 | C | CT | 47 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0111 others(44): Show |
50 | HG00438.hp1 HG00597.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.694+1645dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526539 | ||||||
| chr2:227526539 | C | CTT | 14 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(11): Show |
16 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.694+1644_694+1645d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526539 | ||||||
| chr2:227526539 | CT | C | 64 | a0001c0001t0001g0144 a0001c0001t0004g0193 a0001c0002t0002g0002 others(61): Show |
68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.694+1645delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526539 | ||||||
| chr2:227526736 | G | A | 2 | a0001c0001t0016g0300 a0001c0001t0016g0301 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.694+1821G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526736 | |||||||
| chr2:227526763 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.694+1848C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526763 | |||||||
| chr2:227527036 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.694+2121T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527036 | |||||||
| chr2:227527054 | A | G | 7 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(4): Show |
7 | HG00639.hp2 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.694+2139A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527054 | |||||||
| chr2:227527370 | C | T | 5 | a0001c0003t0003g0063 a0001c0003t0003g0071 a0001c0003t0013g0072 others(2): Show |
5 | NA18943.hp1 NA18944.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.694+2455C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527370 | |||||||
| chr2:227527382 | T | C | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.694+2467T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527382 | |||||||
| chr2:227527482 | A | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.694+2567A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527482 | |||||||
| chr2:227527498 | C | T | 2 | a0001c0001t0005g0310 a0001c0001t0005g0311 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.694+2583C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527498 | |||||||
| chr2:227527776 | G | A | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.694+2861G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527776 | |||||||
| chr2:227527806 | T | C | 3 | a0001c0001t0005g0003 a0001c0001t0005g0307 a0001c0001t0005g0308 |
5 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.694+2891T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527806 | |||||||
| chr2:227527914 | C | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.694+2999C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527914 | |||||||
| chr2:227528115 | C | G | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.695-2976C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528115 | |||||||
| chr2:227528125 | A | G | 2 | a0001c0001t0023g0024 a0001c0001t0023g0028 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.695-2966A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528125 | |||||||
| chr2:227528369 | C | T | 1 | a0001c0002t0002g0247 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.695-2722C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528369 | |||||||
| chr2:227528406 | A | T | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.695-2685A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528406 | |||||||
| chr2:227528452 | C | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(144): Show |
152 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.695-2639C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528452 | |||||||
| chr2:227528567 | T | C | 1 | a0001c0001t0011g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.695-2524T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528567 | |||||||
| chr2:227528674 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.695-2417T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528674 | |||||||
| chr2:227528772 | T | C | 2 | a0001c0005t0014g0029 a0001c0005t0014g0030 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.695-2319T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528772 | |||||||
| chr2:227528821 | T | C | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.695-2270T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528821 | |||||||
| chr2:227529107 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.695-1984C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529107 | |||||||
| chr2:227529208 | T | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(190): Show |
202 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.695-1883T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529208 | |||||||
| chr2:227529270 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.695-1821T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529270 | |||||||
| chr2:227529289 | C | A | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-1802C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529289 | |||||||
| chr2:227529341 | T | A | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.695-1750T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529341 | |||||||
| chr2:227529342 | A | T | 2 | a0001c0005t0014g0029 a0001c0005t0014g0030 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.695-1749A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529342 | |||||||
| chr2:227529351 | T | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.695-1740T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529351 | |||||||
| chr2:227529425 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.695-1666A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529425 | |||||||
| chr2:227529444 | G | A | 1 | a0001c0001t0033g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.695-1647G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529444 | |||||||
| chr2:227530009 | G | A | 1 | a0001c0003t0003g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.695-1082G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227530009 | |||||||
| chr2:227530290 | G | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.695-801G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227530290 | |||||||
| chr2:227530392 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0017g0229 a0001c0001t0017g0231 |
3 | HG03209.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.695-699A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227530392 | |||||||
| chr2:227530636 | AT | A | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.695-453delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227530636 | ||||||
| chr2:227530663 | AAGTATTT others(18): Show |
A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.695-426_695-402del others(25): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227530663 | ||||||
| chr2:227530856 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
219 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.695-235G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227530856 | |||||||
| chr2:227531312 | C | A | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.814+102C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531312 | |||||||
| chr2:227531495 | A | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.814+285A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531495 | |||||||
| chr2:227531521 | G | GTC | 4 | a0001c0004t0006g0004 a0001c0004t0006g0040 a0001c0004t0006g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.814+315_814+316dup others(2): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227531521 | ||||||
| chr2:227531525 | C | CT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(143): Show |
151 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.814+330dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227531525 | ||||||
| chr2:227531525 | C | CTT | 34 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(31): Show |
35 | HG00558.hp2 HG00642.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.814+329_814+330dup others(2): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227531525 | ||||||
| chr2:227531526 | T | TC | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0225 |
3 | HG03017.hp2 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.814+316_814+317ins others(1): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531526 | |||||||
| chr2:227531596 | A | AT | 10 | a0001c0001t0005g0307 a0001c0004t0006g0005 a0001c0004t0006g0038 others(7): Show |
11 | HG00738.hp2 HG01515.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.814+402dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227531596 | ||||||
| chr2:227531596 | AT | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(150): Show |
158 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.814+402delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227531596 | ||||||
| chr2:227531620 | G | T | 1 | a0001c0001t0018g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.814+410G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531620 | |||||||
| chr2:227531795 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.814+585A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531795 | |||||||
| chr2:227531933 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.814+723G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531933 | |||||||
| chr2:227532050 | C | G | 2 | a0001c0001t0005g0087 a0001c0001t0005g0305 |
2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.814+840C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532050 | |||||||
| chr2:227532168 | T | C | 1 | a0001c0001t0032g0096 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.814+958T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532168 | |||||||
| chr2:227532287 | G | A | 1 | a0001c0001t0041g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.814+1077G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532287 | |||||||
| chr2:227532383 | A | G | 1 | a0001c0004t0009g0048 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.815-1166A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532383 | |||||||
| chr2:227532585 | A | G | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.815-964A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532585 | |||||||
| chr2:227532610 | C | G | 1 | a0001c0001t0021g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.815-939C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532610 | |||||||
| chr2:227532850 | T | G | 111 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
113 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.815-699T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532850 | |||||||
| chr2:227532878 | A | G | 1 | a0001c0002t0002g0020 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.815-671A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532878 | |||||||
| chr2:227532914 | AATGT | A | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-632_815-629del others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227532914 | ||||||
| chr2:227532925 | T | C | 69 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(66): Show |
70 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.815-624T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532925 | |||||||
| chr2:227533285 | A | AC | 180 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
187 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.815-260dupC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227533285 | ||||||
| chr2:227533386 | T | C | 1 | a0001c0002t0002g0243 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.815-163T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227533386 | |||||||
| chr2:227533510 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.815-39A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227533510 | |||||||
| chr2:227533864 | A | G | 1 | a0001c0001t0025g0220 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1024+106A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227533864 | |||||||
| chr2:227534039 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1024+281T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534039 | |||||||
| chr2:227534112 | G | A | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1024+354G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534112 | |||||||
| chr2:227534152 | T | A | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1024+394T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534152 | |||||||
| chr2:227534385 | A | G | 1 | a0001c0001t0040g0142 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1025-460A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534385 | |||||||
| chr2:227534696 | G | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1025-149G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534696 | |||||||
| chr2:227534764 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(236): Show |
248 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1025-81T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534764 | |||||||
| chr2:227534827 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0200 |
2 | NA19085.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1025-18G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534827 | |||||||
| chr2:227535369 | T | C | 2 | a0001c0001t0005g0306 a0001c0001t0005g0312 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1205+344T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227535369 | |||||||
| chr2:227535461 | C | A | 1 | a0001c0002t0002g0277 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1205+436C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227535461 | |||||||
| chr2:227535737 | G | A | 60 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(57): Show |
64 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.1205+712G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227535737 | |||||||
| chr2:227535861 | C | T | 13 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(10): Show |
13 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1206-764C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227535861 | |||||||
| chr2:227536051 | G | A | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206-574G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536051 | |||||||
| chr2:227536062 | C | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206-563C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536062 | |||||||
| chr2:227536169 | A | AC | 5 | a0001c0004t0006g0004 a0001c0004t0006g0040 a0001c0004t0006g0052 others(2): Show |
6 | HG02451.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206-456_1206-455i others(3): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536169 | |||||||
| chr2:227536170 | G | C | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206-455G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536170 | |||||||
| chr2:227536322 | T | C | 1 | a0001c0001t0033g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1206-303T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536322 | |||||||
| chr2:227536377 | A | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206-248A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536377 | |||||||
| chr2:227536579 | T | C | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1206-46T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536579 | |||||||
| chr2:227536590 | GA | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206-27delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 227536590 | ||||||
| chr2:227537494 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1378+501A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537494 | |||||||
| chr2:227537546 | T | C | 5 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0147 others(2): Show |
5 | HG00558.hp1 HG02135.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+553T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537546 | |||||||
| chr2:227537569 | C | T | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1378+576C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537569 | |||||||
| chr2:227537673 | T | C | 2 | a0001c0001t0005g0310 a0001c0001t0005g0311 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1378+680T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537673 | |||||||
| chr2:227537725 | A | G | 2 | a0001c0001t0020g0152 a0001c0001t0020g0162 |
2 | HG02015.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1378+732A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537725 | |||||||
| chr2:227537910 | A | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+917A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537910 | |||||||
| chr2:227537979 | G | C | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1378+986G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537979 | |||||||
| chr2:227538099 | A | G | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1378+1106A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538099 | |||||||
| chr2:227538121 | G | A | 20 | a0001c0003t0003g0062 a0001c0003t0003g0063 a0001c0003t0003g0064 others(17): Show |
20 | HG00423.hp1 HG00609.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1378+1128G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538121 | |||||||
| chr2:227538457 | G | T | 1 | a0001c0004t0006g0050 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1378+1464G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538457 | |||||||
| chr2:227538469 | T | C | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1378+1476T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538469 | |||||||
| chr2:227538535 | C | A | 1 | a0001c0001t0001g0016 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1378+1542C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538535 | |||||||
| chr2:227538622 | G | A | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02896.hp1 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1378+1629G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538622 | |||||||
| chr2:227538839 | A | G | 1 | a0001c0002t0002g0290 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1378+1846A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538839 | |||||||
| chr2:227538863 | C | G | 2 | a0001c0001t0030g0239 a0001c0001t0031g0191 |
2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1378+1870C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538863 | |||||||
| chr2:227539087 | A | G | 65 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(62): Show |
69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1378+2094A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539087 | |||||||
| chr2:227539226 | T | A | 1 | a0001c0003t0003g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1378+2233T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539226 | |||||||
| chr2:227539289 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1378+2296A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539289 | |||||||
| chr2:227539442 | C | CAAAAAAA | 18 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(15): Show |
20 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.1378+2451_1378+245 others(11): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227539442 | ||||||
| chr2:227539451 | C | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1378+2458C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539451 | |||||||
| chr2:227539457 | A | AAAAAAAA others(3): Show |
3 | a0001c0001t0001g0217 a0001c0001t0011g0228 a0001c0001t0015g0235 |
3 | HG03471.hp1 NA18522.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1378+2464_1378+246 others(14): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539457 | |||||||
| chr2:227539457 | A | AAAAAAAA others(2): Show |
36 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0103 others(33): Show |
36 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1378+2464_1378+246 others(13): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539457 | |||||||
| chr2:227539457 | A | AAAAAAAA others(1): Show |
118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
123 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1378+2464_1378+246 others(12): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539457 | |||||||
| chr2:227539521 | G | A | 20 | a0001c0003t0003g0062 a0001c0003t0003g0063 a0001c0003t0003g0064 others(17): Show |
20 | HG00423.hp1 HG00609.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1378+2528G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539521 | |||||||
| chr2:227539665 | A | T | 5 | a0001c0003t0003g0064 a0001c0003t0003g0067 a0001c0003t0003g0069 others(2): Show |
5 | HG01123.hp2 HG01934.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+2672A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539665 | |||||||
| chr2:227539746 | C | CA | 56 | a0001c0001t0001g0016 a0001c0001t0001g0124 a0001c0001t0001g0129 others(53): Show |
56 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.1378+2775dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227539746 | ||||||
| chr2:227539746 | CA | C | 35 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(32): Show |
35 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1378+2775delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227539746 | ||||||
| chr2:227539746 | CAA | C | 8 | a0001c0004t0006g0005 a0001c0004t0006g0038 a0001c0004t0006g0050 others(5): Show |
9 | HG02129.hp1 HG02615.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378+2774_1378+277 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227539746 | ||||||
| chr2:227539746 | CAAA | C | 11 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0040 others(8): Show |
12 | HG02109.hp2 HG02135.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1378+2773_1378+277 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227539746 | ||||||
| chr2:227539747 | A | C | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1378+2754A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539747 | |||||||
| chr2:227539851 | T | C | 8 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0025 others(5): Show |
8 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+2858T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539851 | |||||||
| chr2:227539913 | G | A | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+2920G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539913 | |||||||
| chr2:227540113 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1378+3120G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540113 | |||||||
| chr2:227540197 | G | GT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1378+3218dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227540197 | ||||||
| chr2:227540260 | T | G | 1 | a0001c0003t0003g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1378+3267T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540260 | |||||||
| chr2:227540288 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1378+3295C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540288 | |||||||
| chr2:227540341 | C | A | 1 | a0001c0001t0001g0149 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1378+3348C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540341 | |||||||
| chr2:227540369 | C | T | 1 | a0001c0001t0041g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1378+3376C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540369 | |||||||
| chr2:227540392 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1378+3399G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540392 | |||||||
| chr2:227540454 | T | C | 4 | a0001c0004t0006g0004 a0001c0004t0006g0040 a0001c0004t0006g0041 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+3461T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540454 | |||||||
| chr2:227540465 | G | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1378+3472G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540465 | |||||||
| chr2:227540641 | T | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+3648T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540641 | |||||||
| chr2:227540654 | G | A | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+3661G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540654 | |||||||
| chr2:227540670 | C | G | 8 | a0001c0002t0002g0275 a0001c0002t0002g0276 a0001c0002t0002g0277 others(5): Show |
8 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+3677C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540670 | |||||||
| chr2:227540701 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0185 |
2 | HG00642.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1378+3708G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540701 | |||||||
| chr2:227540774 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1378+3781G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540774 | |||||||
| chr2:227540991 | T | C | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+3998T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540991 | |||||||
| chr2:227540992 | G | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+3999G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540992 | |||||||
| chr2:227541022 | C | T | 1 | a0001c0004t0006g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1378+4029C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541022 | |||||||
| chr2:227541042 | T | G | 1 | a0001c0001t0017g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1378+4049T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541042 | |||||||
| chr2:227541084 | C | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+4091C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541084 | |||||||
| chr2:227541248 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1378+4255T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541248 | |||||||
| chr2:227541285 | A | G | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+4292A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541285 | |||||||
| chr2:227541491 | T | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
219 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.1378+4498T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541491 | |||||||
| chr2:227541516 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02132.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1378+4523A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541516 | |||||||
| chr2:227541619 | T | A | 2 | a0001c0003t0003g0063 a0001c0003t0003g0071 |
2 | NA18947.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1378+4626T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541619 | |||||||
| chr2:227541668 | T | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1378+4675T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541668 | |||||||
| chr2:227541677 | A | T | 4 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(1): Show |
4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+4684A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541677 | |||||||
| chr2:227541694 | C | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1378+4701C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541694 | |||||||
| chr2:227541820 | A | G | 1 | a0001c0001t0011g0228 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1378+4827A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541820 | |||||||
| chr2:227541885 | G | T | 13 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(10): Show |
15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1378+4892G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541885 | |||||||
| chr2:227541987 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1378+4994G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541987 | |||||||
| chr2:227541990 | C | G | 5 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+4997C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541990 | |||||||
| chr2:227542248 | A | T | 1 | a0001c0003t0003g0085 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1378+5255A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542248 | |||||||
| chr2:227542298 | C | T | 2 | a0001c0001t0011g0226 a0001c0001t0026g0227 |
2 | HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1378+5305C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542298 | |||||||
| chr2:227542314 | T | A | 1 | a0001c0002t0002g0284 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1378+5321T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542314 | |||||||
| chr2:227542389 | A | T | 2 | a0001c0001t0005g0310 a0001c0001t0005g0311 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1378+5396A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542389 | |||||||
| chr2:227542404 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1378+5411A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542404 | |||||||
| chr2:227542439 | C | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0108 |
3 | HG01109.hp2 HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1378+5446C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542439 | |||||||
| chr2:227542528 | A | G | 57 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(54): Show |
61 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1378+5535A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542528 | |||||||
| chr2:227542948 | G | A | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1378+5955G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542948 | |||||||
| chr2:227542984 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(173): Show |
183 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1378+5991C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542984 | |||||||
| chr2:227543077 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(244): Show |
257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.1378+6084G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543077 | |||||||
| chr2:227543089 | G | A | 1 | a0001c0002t0002g0264 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1378+6096G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543089 | |||||||
| chr2:227543222 | T | C | 5 | a0001c0002t0002g0013 a0001c0002t0002g0242 a0001c0002t0002g0243 others(2): Show |
6 | HG00408.hp2 NA18950.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+6229T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543222 | |||||||
| chr2:227543421 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1378+6428T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543421 | |||||||
| chr2:227543529 | A | C | 3 | a0001c0001t0005g0003 a0001c0001t0005g0307 a0001c0001t0005g0308 |
5 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+6536A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543529 | |||||||
| chr2:227543622 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0121 others(18): Show |
24 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1378+6629G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543622 | |||||||
| chr2:227543664 | A | G | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+6671A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543664 | |||||||
| chr2:227543776 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1378+6783T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543776 | |||||||
| chr2:227543839 | C | CTGT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1378+6847_1378+684 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227543839 | ||||||
| chr2:227543851 | C | CAT | 154 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1378+6865_1378+686 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227543851 | ||||||
| chr2:227543935 | T | G | 1 | a0001c0002t0002g0291 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1378+6942T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543935 | |||||||
| chr2:227543964 | T | G | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1378+6971T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543964 | |||||||
| chr2:227543987 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1378+6994A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543987 | |||||||
| chr2:227543997 | C | A | 1 | a0001c0001t0041g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1378+7004C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543997 | |||||||
| chr2:227544146 | C | CT | 6 | a0001c0002t0002g0015 a0001c0002t0002g0245 a0001c0002t0002g0251 others(3): Show |
6 | HG01255.hp1 HG02071.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+7179dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227544146 | ||||||
| chr2:227544146 | CT | C | 71 | a0001c0001t0005g0310 a0001c0001t0005g0311 a0001c0001t0008g0021 others(68): Show |
73 | HG00423.hp1 HG00609.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1378+7179delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227544146 | ||||||
| chr2:227544146 | CTT | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0098 a0001c0001t0001g0100 others(15): Show |
18 | HG00099.hp1 HG00423.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1378+7178_1378+717 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227544146 | ||||||
| chr2:227544146 | CTTT | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
142 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1378+7177_1378+717 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227544146 | ||||||
| chr2:227544146 | CTTTT | C | 6 | a0001c0001t0001g0105 a0001c0001t0001g0186 a0001c0001t0001g0196 others(3): Show |
6 | HG01081.hp1 HG01515.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+7176_1378+717 others(8): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227544146 | ||||||
| chr2:227544178 | G | A | 5 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0147 others(2): Show |
5 | HG00558.hp1 HG02135.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+7185G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544178 | |||||||
| chr2:227544216 | G | A | 2 | a0001c0003t0003g0058 a0001c0003t0003g0059 |
2 | HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1378+7223G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544216 | |||||||
| chr2:227544290 | G | C | 1 | a0001c0004t0006g0052 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1378+7297G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544290 | |||||||
| chr2:227544368 | A | T | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1378+7375A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544368 | |||||||
| chr2:227544376 | G | A | 5 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(2): Show |
5 | HG00639.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+7383G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544376 | |||||||
| chr2:227544384 | G | A | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1378+7391G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544384 | |||||||
| chr2:227544546 | C | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1379-7413C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544546 | |||||||
| chr2:227544559 | G | A | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1379-7400G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544559 | |||||||
| chr2:227544666 | C | G | 1 | a0001c0002t0002g0290 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1379-7293C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544666 | |||||||
| chr2:227544825 | C | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(143): Show |
151 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1379-7134C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544825 | |||||||
| chr2:227544863 | C | T | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1379-7096C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544863 | |||||||
| chr2:227544941 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1379-7018G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544941 | |||||||
| chr2:227545077 | C | T | 2 | a0001c0003t0003g0065 a0001c0003t0003g0076 |
2 | HG00423.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1379-6882C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545077 | |||||||
| chr2:227545078 | G | A | 15 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(12): Show |
15 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1379-6881G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545078 | |||||||
| chr2:227545091 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1379-6868A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545091 | |||||||
| chr2:227545253 | C | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1379-6706C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545253 | |||||||
| chr2:227545286 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1379-6673T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545286 | |||||||
| chr2:227545328 | C | T | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-6631C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545328 | |||||||
| chr2:227545742 | G | A | 2 | a0001c0001t0005g0310 a0001c0001t0005g0311 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1379-6217G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545742 | |||||||
| chr2:227545781 | A | G | 5 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(2): Show |
5 | HG00639.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379-6178A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545781 | |||||||
| chr2:227545933 | C | T | 5 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(2): Show |
5 | HG00639.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379-6026C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545933 | |||||||
| chr2:227545940 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1379-6019C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545940 | |||||||
| chr2:227546098 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1379-5861C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546098 | |||||||
| chr2:227546128 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1379-5831C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546128 | |||||||
| chr2:227546198 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0121 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1379-5761G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546198 | |||||||
| chr2:227546201 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1379-5758C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546201 | |||||||
| chr2:227546220 | C | T | 32 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(29): Show |
32 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1379-5739C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546220 | |||||||
| chr2:227546289 | G | A | 1 | a0001c0001t0019g0199 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1379-5670G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546289 | |||||||
| chr2:227546297 | C | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1379-5662C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546297 | |||||||
| chr2:227546320 | C | T | 1 | a0001c0002t0002g0290 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1379-5639C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546320 | |||||||
| chr2:227546327 | T | A | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1379-5632T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546327 | |||||||
| chr2:227546441 | G | A | 2 | a0001c0002t0002g0257 a0001c0002t0002g0259 |
2 | HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1379-5518G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546441 | |||||||
| chr2:227546471 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1379-5488T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546471 | |||||||
| chr2:227546480 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1379-5479G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546480 | |||||||
| chr2:227546595 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(143): Show |
151 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1379-5364C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546595 | |||||||
| chr2:227546596 | G | A | 2 | a0001c0001t0016g0300 a0001c0001t0016g0301 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1379-5363G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546596 | |||||||
| chr2:227546640 | T | G | 2 | a0001c0002t0002g0251 a0001c0002t0002g0268 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1379-5319T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546640 | |||||||
| chr2:227546943 | C | T | 65 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(62): Show |
69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1379-5016C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546943 | |||||||
| chr2:227546958 | T | G | 1 | a0001c0002t0002g0254 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1379-5001T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546958 | |||||||
| chr2:227547016 | A | G | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1379-4943A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547016 | |||||||
| chr2:227547019 | C | T | 1 | a0001c0004t0006g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1379-4940C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547019 | |||||||
| chr2:227547038 | A | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | HG02055.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1379-4921A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547038 | |||||||
| chr2:227547067 | A | T | 1 | a0001c0001t0005g0304 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1379-4892A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547067 | |||||||
| chr2:227547346 | TC | T | 7 | a0001c0002t0007g0006 a0001c0002t0007g0089 a0001c0002t0007g0090 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1379-4610delC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227547346 | ||||||
| chr2:227547397 | A | G | 1 | a0001c0001t0032g0096 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1379-4562A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547397 | |||||||
| chr2:227547552 | G | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1379-4407G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547552 | |||||||
| chr2:227547574 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1379-4385A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547574 | |||||||
| chr2:227547582 | C | T | 19 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(16): Show |
19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.1379-4377C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547582 | |||||||
| chr2:227547668 | G | A | 2 | a0001c0005t0014g0029 a0001c0005t0014g0030 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1379-4291G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547668 | |||||||
| chr2:227547869 | G | C | 4 | a0001c0001t0011g0094 a0001c0001t0011g0226 a0001c0001t0011g0228 others(1): Show |
4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379-4090G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547869 | |||||||
| chr2:227547916 | T | C | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1379-4043T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547916 | |||||||
| chr2:227548081 | G | A | 15 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(12): Show |
17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1379-3878G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548081 | |||||||
| chr2:227548106 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1379-3853T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548106 | |||||||
| chr2:227548111 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1379-3848A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548111 | |||||||
| chr2:227548195 | TG | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1379-3761delG | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227548195 | ||||||
| chr2:227548217 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0143 |
2 | HG02015.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1379-3742A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548217 | |||||||
| chr2:227548237 | G | A | 1 | a0001c0001t0008g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1379-3722G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548237 | |||||||
| chr2:227548241 | A | G | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-3718A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548241 | |||||||
| chr2:227548280 | C | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1379-3679C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548280 | |||||||
| chr2:227548426 | G | A | 17 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(14): Show |
17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1379-3533G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548426 | |||||||
| chr2:227548660 | G | A | 1 | a0001c0004t0006g0054 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1379-3299G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548660 | |||||||
| chr2:227548669 | G | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(155): Show |
163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1379-3290G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548669 | |||||||
| chr2:227548686 | C | T | 1 | a0001c0001t0033g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1379-3273C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548686 | |||||||
| chr2:227548713 | G | A | 1 | a0001c0001t0032g0096 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1379-3246G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548713 | |||||||
| chr2:227548764 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1379-3195C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548764 | |||||||
| chr2:227548765 | G | A | 1 | a0001c0001t0004g0192 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1379-3194G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548765 | |||||||
| chr2:227548773 | T | C | 1 | a0001c0004t0006g0038 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1379-3186T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548773 | |||||||
| chr2:227548853 | C | T | 1 | a0001c0002t0002g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1379-3106C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548853 | |||||||
| chr2:227548932 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1379-3027G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548932 | |||||||
| chr2:227549011 | C | CT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1379-2937dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227549011 | ||||||
| chr2:227549127 | C | T | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1379-2832C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549127 | |||||||
| chr2:227549238 | C | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02257.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1379-2721C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549238 | |||||||
| chr2:227549315 | A | G | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-2644A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549315 | |||||||
| chr2:227549629 | A | G | 1 | a0001c0002t0007g0093 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1379-2330A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549629 | |||||||
| chr2:227549643 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1379-2316A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549643 | |||||||
| chr2:227549667 | T | G | 1 | a0001c0001t0001g0217 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1379-2292T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549667 | |||||||
| chr2:227549773 | G | A | 13 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(10): Show |
13 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1379-2186G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549773 | |||||||
| chr2:227549803 | T | A | 3 | a0001c0003t0003g0055 a0001c0003t0003g0073 a0001c0003t0003g0074 |
3 | HG00099.hp1 HG02735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1379-2156T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549803 | |||||||
| chr2:227549901 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1379-2058T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549901 | |||||||
| chr2:227549989 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1379-1970G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549989 | |||||||
| chr2:227550071 | C | G | 1 | a0001c0001t0001g0201 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1379-1888C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550071 | |||||||
| chr2:227550258 | A | G | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1379-1701A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550258 | |||||||
| chr2:227550498 | C | T | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1379-1461C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550498 | |||||||
| chr2:227550532 | TGTC | T | 9 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(6): Show |
9 | HG00099.hp1 HG01952.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-1423_1379-142 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227550532 | ||||||
| chr2:227550764 | A | G | 1 | a0001c0001t0017g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1379-1195A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550764 | |||||||
| chr2:227550810 | C | T | 1 | a0001c0001t0019g0165 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1379-1149C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550810 | |||||||
| chr2:227550887 | G | T | 2 | a0001c0002t0002g0251 a0001c0002t0002g0268 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1379-1072G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550887 | |||||||
| chr2:227551044 | A | G | 1 | a0001c0001t0031g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1379-915A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551044 | |||||||
| chr2:227551093 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1379-866C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551093 | |||||||
| chr2:227551279 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1379-680C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551279 | |||||||
| chr2:227551459 | A | G | 1 | a0001c0002t0002g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1379-500A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551459 | |||||||
| chr2:227551468 | A | G | 1 | a0001c0002t0022g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1379-491A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551468 | |||||||
| chr2:227551512 | A | T | 20 | a0001c0001t0041g0086 a0001c0004t0006g0004 a0001c0004t0006g0005 others(17): Show |
22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1379-447A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551512 | |||||||
| chr2:227551558 | G | T | 1 | a0001c0001t0032g0096 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1379-401G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551558 | |||||||
| chr2:227551782 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(173): Show |
183 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1379-177C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551782 | |||||||
| chr2:227552145 | A | C | 2 | a0001c0001t0016g0300 a0001c0001t0016g0301 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1537+28A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552145 | |||||||
| chr2:227552295 | A | T | 13 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(10): Show |
15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1537+178A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552295 | |||||||
| chr2:227552466 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1537+349T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552466 | |||||||
| chr2:227552557 | T | G | 1 | a0001c0001t0001g0127 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1537+440T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552557 | |||||||
| chr2:227552740 | G | T | 1 | a0001c0002t0002g0277 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1537+623G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552740 | |||||||
| chr2:227552827 | C | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0121 others(17): Show |
23 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1537+710C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552827 | |||||||
| chr2:227552853 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1537+736T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552853 | |||||||
| chr2:227552862 | G | A | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1537+745G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552862 | |||||||
| chr2:227552957 | G | A | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1538-747G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552957 | |||||||
| chr2:227553000 | C | CA | 162 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
167 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1538-683dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553000 | ||||||
| chr2:227553000 | C | CAA | 27 | a0001c0001t0001g0145 a0001c0001t0001g0151 a0001c0001t0001g0169 others(24): Show |
29 | HG00621.hp1 HG00621.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1538-684_1538-683d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553000 | ||||||
| chr2:227553000 | C | CAAA | 14 | a0001c0001t0005g0003 a0001c0001t0005g0087 a0001c0001t0005g0302 others(11): Show |
16 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1538-685_1538-683d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553000 | ||||||
| chr2:227553000 | CA | C | 30 | a0001c0001t0001g0125 a0001c0002t0002g0241 a0001c0002t0007g0091 others(27): Show |
30 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1538-683delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553000 | ||||||
| chr2:227553329 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1538-375C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553329 | |||||||
| chr2:227553436 | CAGTGAGC others(4): Show |
C | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-266_1538-256d others(13): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553436 | ||||||
| chr2:227553448 | A | T | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-256A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553448 | |||||||
| chr2:227553449 | T | C | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-255T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553449 | |||||||
| chr2:227553458 | T | A | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-246T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553458 | |||||||
| chr2:227553459 | GGACTCTG others(49): Show |
G | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-244_1538-189d others(58): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553459 | |||||||
| chr2:227553495 | C | CA | 163 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1538-192dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553495 | ||||||
| chr2:227553495 | C | CAA | 6 | a0001c0001t0001g0163 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG00597.hp2 HG01081.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1538-193_1538-192d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553495 | ||||||
| chr2:227553495 | CA | C | 8 | a0001c0002t0002g0241 a0001c0002t0007g0006 a0001c0002t0007g0089 others(5): Show |
9 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1538-192delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553495 | ||||||
| chr2:227553518 | T | G | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-186T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553518 | |||||||
| chr2:227553519 | T | C | 2 | a0001c0001t0018g0031 a0001c0001t0018g0032 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-185T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553519 | |||||||
| chr2:227553527 | A | G | 2 | a0001c0001t0032g0096 a0001c0001t0041g0086 |
2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1538-177A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553527 | |||||||
| chr2:227553544 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1538-160T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553544 | |||||||
| chr2:227553547 | T | C | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1538-157T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553547 | |||||||
| chr2:227553577 | A | G | 4 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1538-127A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553577 | |||||||
| chr2:227553894 | TATATTG | T | 29 | a0001c0003t0003g0055 a0001c0003t0003g0057 a0001c0003t0003g0058 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1629+104_1629+109d others(8): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 227553894 | ||||||
| chr2:227553915 | A | G | 2 | a0001c0001t0017g0229 a0001c0001t0017g0231 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1629+120A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227553915 | |||||||
| chr2:227553953 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1629+158A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227553953 | |||||||
| chr2:227554013 | A | C | 9 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0023 others(6): Show |
9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1629+218A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227554013 | |||||||
| chr2:227554028 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1629+233A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227554028 | |||||||
| chr2:227554141 | G | C | 65 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(62): Show |
69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1630-295G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227554141 | |||||||
| chr2:227554241 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(128): Show |
136 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1630-195A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227554241 | |||||||
| chr2:227554265 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1630-171T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227554265 |