Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 115548 |
| ensemblid | ENSG00000157107.14 |
| hgncid | 25180 |
| symbol | FCHO2 |
| name | FCH and mu domain containing endocytic adaptor 2 |
| refseq_nuc | NM_138782.3 |
| refseq_prot | NP_620137.2 |
| ensembl_nuc | ENST00000430046.7 |
| ensembl_prot | ENSP00000393776.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 72956041 |
| end | 73090522 |
| strand | + |
| ver | v1.2 |
| region | chr5:72956041-73090522 |
| region5000 | chr5:72951041-73095522 |
| regionname0 | FCHO2_chr5_72956041_73090522 |
| regionname5000 | FCHO2_chr5_72951041_73095522 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 810 | 211 | 42 | 39 | 101 | 5 | 22 | 73 | FCHO2_chr5_72951041_73095522 | FCHO2 | MVMAY others(805): Show |
chr5 | 72951041 | 73095522 |
| a0002 | 0/0 | 810 | 71 | 24 | 9 | 30 | 1 | 7 | 20 | FCHO2_chr5_72951041_73095522 | FCHO2 | MVMAY others(805): Show |
chr5 | 72951041 | 73095522 |
| a0003 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | MVMAY others(805): Show |
chr5 | 72951041 | 73095522 |
| a0004 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | MVMAY others(805): Show |
chr5 | 72951041 | 73095522 |
| a0005 | 0/0 | 810 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | MVMAY others(805): Show |
chr5 | 72951041 | 73095522 |
| a0006 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | MVMAY others(805): Show |
chr5 | 72951041 | 73095522 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2430 | 115 | 15 | 25 | 57 | 2 | 15 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 | ||
| a0001c0003 | 0/0 | 2430 | 51 | 25 | 10 | 7 | 2 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 | ||
| a0001c0004 | 0/1 | 2430 | 38 | 2 | 3 | 31 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 | ||
| a0001c0005 | 0/0 | 2430 | 5 | 0 | 0 | 5 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 | ||
| a0001c0009 | 0/0 | 2430 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 | ||
| a0001c0010 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 | ||
| a0002c0002 | 0/0 | 2430 | 71 | 24 | 9 | 30 | 1 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 | ||
| a0003c0006 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 | ||
| a0004c0008 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 | ||
| a0005c0011 | 0/0 | 2430 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 | ||
| a0006c0007 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | ATGGT others(2425): Show |
chr5 | 72951041 | 73095522 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4921 | 106 | 14 | 21 | 54 | 2 | 15 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0001t0002 | 1/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0001t0007 | 0/0 | 4921 | 4 | 1 | 3 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0001t0013 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0001t0015 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0001t0018 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0001t0019 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0003t0003 | 0/0 | 4921 | 6 | 6 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0003t0004 | 0/0 | 4921 | 26 | 1 | 9 | 7 | 2 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0003t0005 | 0/0 | 4921 | 8 | 8 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0003t0006 | 0/0 | 4921 | 4 | 4 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0003t0008 | 0/0 | 4921 | 3 | 3 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0003t0010 | 0/0 | 4921 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0003t0011 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0003t0016 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0004t0003 | 0/0 | 4921 | 34 | 2 | 3 | 29 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0004t0009 | 0/1 | 4921 | 2 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0004t0012 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0004t0014 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0005t0003 | 0/0 | 4921 | 4 | 0 | 0 | 4 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0005t0017 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0009t0001 | 0/0 | 4921 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0001c0010t0003 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0002c0002t0002 | 0/0 | 4921 | 71 | 24 | 9 | 30 | 1 | 7 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0003c0006t0005 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0004c0008t0003 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0005c0011t0004 | 0/0 | 4921 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| a0006c0007t0003 | 0/0 | 4921 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | GTGTT others(4916): Show |
chr5 | 72951041 | 73095522 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0002g0024 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0007g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0013g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0015g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0018g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0001t0019g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0011g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0003t0016g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0009g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0009g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0012g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0004t0014g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0005t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0005t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0005t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0005t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0005t0017g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0009t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0001c0010t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0003c0006t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0004c0008t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0005c0011t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| a0006c0007t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0004 | g0085 | EUR | GBR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0009 | EUR | GBR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00423 | hp1 | a0001 | c0003 | t0004 | g0094 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00438 | hp2 | a0001 | c0003 | t0004 | g0095 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00558 | hp2 | a0001 | c0004 | t0003 | g0265 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00609 | hp1 | a0001 | c0004 | t0003 | g0263 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00609 | hp2 | a0001 | c0003 | t0004 | g0080 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00621 | hp2 | a0001 | c0004 | t0003 | g0238 | EAS | CHS | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00735 | hp1 | a0001 | c0004 | t0003 | g0242 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01069 | hp2 | a0001 | c0003 | t0004 | g0072 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01071 | hp1 | a0001 | c0003 | t0004 | g0071 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0046 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01081 | hp1 | a0001 | c0004 | t0003 | g0245 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0230 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01099 | hp2 | a0001 | c0003 | t0004 | g0088 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01106 | hp2 | a0001 | c0003 | t0016 | g0096 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01168 | hp1 | a0001 | c0003 | t0004 | g0084 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01168 | hp2 | a0001 | c0009 | t0001 | g0126 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01169 | hp2 | a0001 | c0003 | t0004 | g0083 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01192 | hp1 | a0001 | c0001 | t0015 | g0166 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01192 | hp2 | a0001 | c0003 | t0004 | g0070 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0068 | AMR | PUR | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01255 | hp2 | a0001 | c0003 | t0004 | g0075 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01261 | hp2 | a0001 | c0003 | t0004 | g0093 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0227 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0113 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01934 | hp1 | a0001 | c0001 | t0007 | g0229 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01934 | hp2 | a0001 | c0004 | t0003 | g0266 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02027 | hp2 | a0001 | c0004 | t0003 | g0271 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02056 | hp1 | a0001 | c0004 | t0012 | g0264 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02071 | hp1 | a0001 | c0004 | t0003 | g0273 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02074 | hp1 | a0001 | c0003 | t0004 | g0081 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02074 | hp2 | a0001 | c0004 | t0003 | g0274 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02080 | hp1 | a0001 | c0004 | t0003 | g0269 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0060 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02145 | hp2 | a0001 | c0003 | t0003 | g0280 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | CDX | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02257 | hp1 | a0001 | c0003 | t0008 | g0109 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02280 | hp1 | a0001 | c0004 | t0003 | g0244 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02280 | hp2 | a0001 | c0003 | t0011 | g0231 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0112 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02451 | hp1 | a0001 | c0003 | t0005 | g0003 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02451 | hp2 | a0001 | c0003 | t0005 | g0105 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02523 | hp1 | a0001 | c0004 | t0003 | g0237 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02572 | hp1 | a0001 | c0003 | t0006 | g0102 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02602 | hp2 | a0001 | c0003 | t0004 | g0074 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02615 | hp1 | a0001 | c0003 | t0010 | g0011 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02615 | hp2 | a0001 | c0003 | t0004 | g0092 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02622 | hp1 | a0001 | c0003 | t0005 | g0233 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02630 | hp1 | a0001 | c0003 | t0005 | g0234 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02630 | hp2 | a0001 | c0003 | t0010 | g0010 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02723 | hp1 | a0003 | c0006 | t0005 | g0004 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0052 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02809 | hp2 | a0004 | c0008 | t0003 | g0279 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02818 | hp1 | a0001 | c0003 | t0006 | g0101 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0042 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0099 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03017 | hp2 | a0005 | c0011 | t0004 | g0089 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03041 | hp2 | a0001 | c0003 | t0006 | g0100 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0053 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03098 | hp2 | a0001 | c0003 | t0005 | g0107 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0054 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0278 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03139 | hp2 | a0001 | c0003 | t0008 | g0111 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03225 | hp2 | a0001 | c0003 | t0003 | g0276 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0050 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0049 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03486 | hp2 | a0001 | c0003 | t0005 | g0108 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03491 | hp1 | a0001 | c0003 | t0004 | g0086 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0012 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03516 | hp1 | a0001 | c0003 | t0008 | g0110 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0063 | AFR | GWD | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03654 | hp2 | a0001 | c0003 | t0004 | g0090 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0019 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03710 | hp2 | a0001 | c0003 | t0004 | g0073 | SAS | PJL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0023 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0025 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG04115 | hp2 | a0001 | c0003 | t0004 | g0087 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0038 | SAS | BEB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG04199 | hp2 | a0001 | c0003 | t0004 | g0091 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG04228 | hp2 | a0001 | c0003 | t0004 | g0079 | SAS | STU | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | YRI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | CHB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18747 | hp1 | a0001 | c0004 | t0003 | g0275 | EAS | CHB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18906 | hp1 | a0001 | c0003 | t0003 | g0098 | AFR | YRI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0061 | AFR | YRI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18939 | hp1 | a0001 | c0005 | t0003 | g0247 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18940 | hp2 | a0001 | c0004 | t0003 | g0254 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18941 | hp2 | a0001 | c0004 | t0003 | g0246 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18942 | hp2 | a0001 | c0004 | t0003 | g0255 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18945 | hp2 | a0001 | c0004 | t0003 | g0270 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18946 | hp1 | a0001 | c0004 | t0003 | g0260 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18951 | hp2 | a0001 | c0004 | t0014 | g0235 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18954 | hp2 | a0006 | c0007 | t0003 | g0267 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18960 | hp2 | a0001 | c0004 | t0003 | g0272 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18965 | hp2 | a0001 | c0004 | t0003 | g0248 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18966 | hp2 | a0001 | c0005 | t0003 | g0257 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18971 | hp1 | a0001 | c0005 | t0017 | g0252 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18982 | hp2 | a0001 | c0004 | t0003 | g0283 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18984 | hp1 | a0001 | c0003 | t0004 | g0078 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18984 | hp2 | a0001 | c0004 | t0003 | g0249 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18989 | hp2 | a0001 | c0010 | t0003 | g0250 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18992 | hp2 | a0001 | c0004 | t0003 | g0262 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18998 | hp1 | a0001 | c0005 | t0003 | g0253 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA18999 | hp2 | a0001 | c0005 | t0003 | g0256 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19001 | hp2 | a0001 | c0004 | t0003 | g0241 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19004 | hp2 | a0001 | c0004 | t0003 | g0239 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19005 | hp1 | a0001 | c0004 | t0003 | g0259 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19010 | hp1 | a0001 | c0004 | t0003 | g0243 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19030 | hp1 | a0001 | c0003 | t0006 | g0103 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0069 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19054 | hp2 | a0001 | c0004 | t0003 | g0261 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19060 | hp1 | a0001 | c0004 | t0003 | g0268 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19062 | hp1 | a0001 | c0004 | t0003 | g0284 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19064 | hp2 | a0001 | c0001 | t0019 | g0157 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19068 | hp1 | a0001 | c0001 | t0018 | g0225 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19068 | hp2 | a0001 | c0004 | t0003 | g0236 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19082 | hp1 | a0001 | c0004 | t0003 | g0240 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19082 | hp2 | a0001 | c0001 | t0013 | g0192 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19084 | hp1 | a0001 | c0003 | t0004 | g0082 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19090 | hp2 | a0001 | c0003 | t0004 | g0077 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA19091 | hp2 | a0001 | c0004 | t0003 | g0258 | EAS | JPT | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA20129 | hp1 | a0001 | c0003 | t0005 | g0104 | AFR | ASW | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ASW | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA20752 | hp2 | a0001 | c0004 | t0009 | g0281 | EUR | TSI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA20805 | hp1 | a0001 | c0003 | t0004 | g0076 | EUR | TSI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | TSI | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | GIH | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01123 | hp1 | a0001 | c0003 | t0004 | g0097 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02109 | hp1 | a0001 | c0003 | t0005 | g0106 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | MSL | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0057 | AFR | USA | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0228 | AFR | USA | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA21309 | hp1 | a0001 | c0004 | t0003 | g0251 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| NA21309 | hp2 | a0001 | c0003 | t0003 | g0277 | AFR | LWK | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0009 | g0282 | REF | REF | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0024 | REF | REF | FCHO2_chr5_72951041_73095522 | FCHO2 | chr5 | 72951041 | 73095522 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:72990838 | G | A | 1 | a0006 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.469G>A | p.Gly157Arg | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/26 | 525/4921 | 469/2433 | 157/810 | chr5 | 72990838 | |||
| chr5:73017229 | A | G | 1 | a0005 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.717A>G | p.Ile239Met | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/26 | 773/4921 | 717/2433 | 239/810 | chr5 | 73017229 | |||
| chr5:73017239 | G | A | 1 | a0004 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.727G>A | p.Ala243Thr | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/26 | 783/4921 | 727/2433 | 243/810 | chr5 | 73017239 | |||
| chr5:73052445 | A | G | 1 | a0002 | 71 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(68): Show |
missense_variant | MODERATE | c.1111A>G | p.Met371Val | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/26 | 1167/4921 | 1111/2433 | 371/810 | chr5 | 73052445 | |||
| chr5:73081754 | A | AACAATTG others(36): Show |
1 | a0001 | 1 | NA19082.hp2 | frameshift_variant | HIGH | c.1981-27_1996dupCAA others(40): Show |
p.Ile666fs | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/26 | 2053/4921 | 1997/2433 | 666/810 | INFO_REALIGN_3_PRIME | chr5 | 73081754 | ||
| chr5:73087637 | A | G | 1 | a0003 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.2294A>G | p.Lys765Arg | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 25/26 | 2350/4921 | 2294/2433 | 765/810 | chr5 | 73087637 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:72990586 | G | A | 1 | a0003c0006 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.309G>A | p.Lys103Lys | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 4/26 | 365/4921 | 309/2433 | 103/810 | chr5 | 72990586 | |||
| chr5:73051396 | A | G | 8 | a0001c0003 a0001c0004 a0001c0005 others(5): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
synonymous_variant | LOW | c.987A>G | p.Thr329Thr | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/26 | 1043/4921 | 987/2433 | 329/810 | chr5 | 73051396 | |||
| chr5:73056078 | A | G | 4 | a0001c0004 a0001c0005 a0001c0010 others(1): Show |
44 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
synonymous_variant | LOW | c.1224A>G | p.Thr408Thr | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/26 | 1280/4921 | 1224/2433 | 408/810 | chr5 | 73056078 | |||
| chr5:73058502 | T | C | 2 | a0001c0005 a0001c0010 |
6 | NA18939.hp1 NA18966.hp2 NA18971.hp1 others(3): Show |
synonymous_variant | LOW | c.1323T>C | p.Ser441Ser | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/26 | 1379/4921 | 1323/2433 | 441/810 | chr5 | 73058502 | |||
| chr5:73081875 | A | G | 1 | a0001c0010 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.2073A>G | p.Lys691Lys | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/26 | 2129/4921 | 2073/2433 | 691/810 | chr5 | 73081875 | |||
| chr5:73087644 | G | A | 1 | a0001c0009 | 1 | HG01168.hp2 | synonymous_variant | LOW | c.2301G>A | p.Thr767Thr | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 25/26 | 2357/4921 | 2301/2433 | 767/810 | chr5 | 73087644 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:73088233 | C | G | 1 | a0001c0001t0019 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*143C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 143 | chr5 | 73088233 | ||||||
| chr5:73088427 | C | T | 1 | a0001c0001t0018 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 337 | chr5 | 73088427 | ||||||
| chr5:73088428 | A | G | 1 | a0001c0005t0017 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 338 | chr5 | 73088428 | ||||||
| chr5:73088435 | C | T | 1 | a0001c0001t0007 | 4 | HG01081.hp2 HG01496.hp2 HG01934.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*345C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 345 | chr5 | 73088435 | ||||||
| chr5:73088441 | C | T | 1 | a0001c0003t0008 | 3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*351C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 351 | chr5 | 73088441 | ||||||
| chr5:73088496 | A | G | 1 | a0001c0003t0010 | 2 | HG02615.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*406A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 406 | chr5 | 73088496 | ||||||
| chr5:73088496 | A | T | 1 | a0001c0003t0006 | 4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*406A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 406 | chr5 | 73088496 | ||||||
| chr5:73088868 | A | G | 1 | a0001c0003t0016 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*778A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 778 | chr5 | 73088868 | ||||||
| chr5:73089026 | C | T | 4 | a0001c0001t0015 a0001c0003t0004 a0001c0003t0016 others(1): Show |
29 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*936C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 936 | chr5 | 73089026 | ||||||
| chr5:73089176 | A | G | 1 | a0001c0004t0014 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1086A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1086 | chr5 | 73089176 | ||||||
| chr5:73089231 | A | G | 7 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(4): Show |
115 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1141A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1141 | chr5 | 73089231 | ||||||
| chr5:73089317 | T | C | 4 | a0001c0001t0015 a0001c0003t0004 a0001c0003t0016 others(1): Show |
29 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1227T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1227 | chr5 | 73089317 | ||||||
| chr5:73089402 | T | C | 1 | a0001c0003t0011 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1312T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1312 | chr5 | 73089402 | ||||||
| chr5:73089626 | A | T | 1 | a0001c0001t0013 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1536A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1536 | chr5 | 73089626 | ||||||
| chr5:73089877 | A | G | 1 | a0001c0003t0011 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1787A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1787 | chr5 | 73089877 | ||||||
| chr5:73090068 | C | T | 1 | a0001c0004t0009 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1978C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1978 | chr5 | 73090068 | ||||||
| chr5:73090086 | A | G | 1 | a0001c0004t0012 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1996A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1996 | chr5 | 73090086 | ||||||
| chr5:73090087 | A | G | 20 | a0001c0001t0015 a0001c0003t0003 a0001c0003t0004 others(17): Show |
99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1997A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 1997 | chr5 | 73090087 | ||||||
| chr5:73090124 | A | T | 1 | a0001c0001t0013 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2034A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 2034 | chr5 | 73090124 | ||||||
| chr5:73090226 | T | A | 1 | a0001c0001t0013 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2136T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 2136 | chr5 | 73090226 | ||||||
| chr5:73090231 | A | T | 1 | a0001c0001t0013 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2141A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 2141 | chr5 | 73090231 | ||||||
| chr5:73090232 | T | C | 1 | a0001c0001t0013 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2142T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 2142 | chr5 | 73090232 | ||||||
| chr5:73090312 | A | G | 11 | a0001c0003t0003 a0001c0003t0008 a0001c0004t0003 others(8): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2222A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 26/26 | 2222 | chr5 | 73090312 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:72956206 | C | T | 2 | a0001c0004t0003g0283 a0001c0004t0003g0284 |
2 | NA18982.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.33+77C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956206 | |||||||
| chr5:72956207 | G | GGGC | 49 | a0001c0003t0003g0276 a0001c0003t0003g0277 a0001c0003t0003g0278 others(46): Show |
49 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.33+91_33+93dupGGC | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72956207 | ||||||
| chr5:72956294 | C | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.33+165C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956294 | |||||||
| chr5:72956480 | C | T | 1 | a0002c0002t0002g0232 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.33+351C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956480 | |||||||
| chr5:72956536 | C | T | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.33+407C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956536 | |||||||
| chr5:72956648 | A | G | 117 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(114): Show |
117 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.33+519A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956648 | |||||||
| chr5:72956787 | C | T | 4 | a0001c0001t0001g0115 a0002c0002t0002g0112 a0002c0002t0002g0113 others(1): Show |
4 | HG01928.hp2 HG02300.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+658C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956787 | |||||||
| chr5:72956888 | C | A | 1 | a0001c0004t0014g0235 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.33+759C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72956888 | |||||||
| chr5:72956896 | G | GT | 12 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.33+778dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72956896 | ||||||
| chr5:72957232 | A | AT | 53 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(50): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.33+1106dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72957232 | ||||||
| chr5:72957236 | C | T | 53 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(50): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.33+1107C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957236 | |||||||
| chr5:72957237 | C | T | 53 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(50): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.33+1108C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957237 | |||||||
| chr5:72957391 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.33+1262T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957391 | |||||||
| chr5:72957392 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.33+1263G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957392 | |||||||
| chr5:72957393 | C | G | 1 | a0001c0001t0001g0116 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.33+1264C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957393 | |||||||
| chr5:72957766 | T | C | 1 | a0001c0004t0003g0236 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.33+1637T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72957766 | |||||||
| chr5:72958237 | A | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.33+2108A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958237 | |||||||
| chr5:72958395 | G | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.33+2266G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958395 | |||||||
| chr5:72958398 | A | G | 4 | a0002c0002t0002g0066 a0002c0002t0002g0067 a0002c0002t0002g0068 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+2269A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958398 | |||||||
| chr5:72958543 | C | T | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.33+2414C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958543 | |||||||
| chr5:72958778 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.33+2649T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958778 | |||||||
| chr5:72958814 | C | G | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.33+2685C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72958814 | |||||||
| chr5:72959098 | A | C | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.33+2969A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959098 | |||||||
| chr5:72959138 | T | C | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+3009T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959138 | |||||||
| chr5:72959183 | A | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33+3054A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959183 | |||||||
| chr5:72959474 | T | C | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.33+3345T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959474 | |||||||
| chr5:72959646 | T | G | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.33+3517T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959646 | |||||||
| chr5:72959660 | A | T | 3 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0004c0008t0003g0279 |
3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.33+3531A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959660 | |||||||
| chr5:72959779 | CT | C | 8 | a0001c0001t0001g0118 a0001c0003t0004g0070 a0001c0003t0005g0003 others(5): Show |
8 | HG00099.hp2 HG01099.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.33+3666delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72959779 | ||||||
| chr5:72959783 | T | C | 115 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(112): Show |
115 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.33+3654T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959783 | |||||||
| chr5:72959784 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.33+3655T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959784 | |||||||
| chr5:72959847 | A | G | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.33+3718A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959847 | |||||||
| chr5:72959981 | T | C | 116 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(113): Show |
116 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.33+3852T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72959981 | |||||||
| chr5:72960026 | C | T | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.33+3897C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960026 | |||||||
| chr5:72960257 | A | G | 1 | a0001c0001t0007g0230 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.33+4128A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960257 | |||||||
| chr5:72960262 | A | C | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+4133A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960262 | |||||||
| chr5:72960311 | G | GA | 213 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(210): Show |
213 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.33+4187dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72960311 | ||||||
| chr5:72960328 | C | T | 44 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(41): Show |
44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.33+4199C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960328 | |||||||
| chr5:72960483 | A | AAAC | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.33+4357_33+4359dup others(3): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72960483 | ||||||
| chr5:72960488 | A | C | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.33+4359A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960488 | |||||||
| chr5:72960607 | C | T | 97 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(94): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.33+4478C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960607 | |||||||
| chr5:72960800 | A | C | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.33+4671A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960800 | |||||||
| chr5:72960804 | C | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33+4675C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72960804 | |||||||
| chr5:72961353 | G | T | 88 | a0001c0001t0001g0116 a0001c0001t0001g0144 a0001c0001t0001g0145 others(85): Show |
88 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.33+5224G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961353 | |||||||
| chr5:72961431 | A | G | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.33+5302A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961431 | |||||||
| chr5:72961541 | T | A | 6 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
6 | HG01106.hp1 HG01123.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.33+5412T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961541 | |||||||
| chr5:72961617 | G | A | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.33+5488G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961617 | |||||||
| chr5:72961625 | G | A | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.33+5496G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961625 | |||||||
| chr5:72961834 | G | A | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.33+5705G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961834 | |||||||
| chr5:72961887 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.33+5758G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961887 | |||||||
| chr5:72961964 | A | G | 4 | a0001c0001t0007g0227 a0001c0001t0007g0228 a0001c0001t0007g0229 others(1): Show |
4 | HG01081.hp2 HG01496.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+5835A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72961964 | |||||||
| chr5:72962003 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.33+5874T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72962003 | |||||||
| chr5:72962630 | C | T | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.34-5868C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72962630 | |||||||
| chr5:72962657 | A | G | 3 | a0001c0003t0010g0010 a0001c0003t0010g0011 a0001c0003t0011g0231 |
3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.34-5841A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72962657 | |||||||
| chr5:72962695 | C | T | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.34-5803C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72962695 | |||||||
| chr5:72962696 | C | T | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.34-5802C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72962696 | |||||||
| chr5:72962891 | C | CA | 59 | a0001c0001t0001g0152 a0001c0003t0003g0098 a0001c0003t0003g0099 others(56): Show |
59 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.34-5595dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72962891 | ||||||
| chr5:72963074 | A | G | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.34-5424A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963074 | |||||||
| chr5:72963086 | T | G | 2 | a0001c0004t0003g0283 a0001c0004t0003g0284 |
2 | NA18982.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.34-5412T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963086 | |||||||
| chr5:72963185 | C | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.34-5313C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963185 | |||||||
| chr5:72963600 | T | TG | 3 | a0002c0002t0002g0063 a0002c0002t0002g0064 a0002c0002t0002g0065 |
3 | HG03471.hp2 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.34-4896dupG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963600 | ||||||
| chr5:72963622 | C | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.34-4876C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963622 | |||||||
| chr5:72963694 | G | A | 2 | a0002c0002t0002g0012 a0002c0002t0002g0013 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.34-4804G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963694 | |||||||
| chr5:72963729 | T | A | 53 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(50): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.34-4769T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963729 | |||||||
| chr5:72963902 | G | GT | 9 | a0002c0002t0002g0055 a0002c0002t0002g0056 a0002c0002t0002g0057 others(6): Show |
9 | HG01884.hp2 HG02027.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.34-4569dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | ||||||
| chr5:72963902 | GT | G | 28 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(25): Show |
28 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.34-4569delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | ||||||
| chr5:72963902 | GTT | G | 114 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(111): Show |
114 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.34-4570_34-4569del others(2): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | ||||||
| chr5:72963902 | GTTT | G | 61 | a0001c0001t0001g0116 a0001c0001t0001g0153 a0001c0001t0001g0154 others(58): Show |
61 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.34-4571_34-4569del others(3): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | ||||||
| chr5:72963902 | GTTTT | G | 7 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(4): Show |
7 | HG02145.hp2 HG02809.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.34-4572_34-4569del others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | ||||||
| chr5:72963902 | GTTTTTTT others(3): Show |
G | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.34-4578_34-4569del others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 72963902 | ||||||
| chr5:72963906 | T | G | 43 | a0001c0004t0003g0236 a0001c0004t0003g0237 a0001c0004t0003g0238 others(40): Show |
43 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.34-4592T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963906 | |||||||
| chr5:72963907 | T | G | 3 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0004c0008t0003g0279 |
3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.34-4591T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963907 | |||||||
| chr5:72963911 | T | G | 1 | a0001c0003t0010g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.34-4587T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963911 | |||||||
| chr5:72963912 | T | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.34-4586T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963912 | |||||||
| chr5:72963918 | T | G | 44 | a0001c0004t0003g0236 a0001c0004t0003g0237 a0001c0004t0003g0238 others(41): Show |
44 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.34-4580T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963918 | |||||||
| chr5:72963919 | T | G | 3 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0004c0008t0003g0279 |
3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.34-4579T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963919 | |||||||
| chr5:72963926 | T | G | 1 | a0002c0002t0002g0015 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.34-4572T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963926 | |||||||
| chr5:72963934 | A | G | 12 | a0002c0002t0002g0049 a0002c0002t0002g0050 a0002c0002t0002g0051 others(9): Show |
12 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.34-4564A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72963934 | |||||||
| chr5:72964416 | C | T | 1 | a0001c0003t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.34-4082C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72964416 | |||||||
| chr5:72964454 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0215 |
2 | NA18986.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.34-4044C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72964454 | |||||||
| chr5:72964619 | C | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.34-3879C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72964619 | |||||||
| chr5:72964677 | C | T | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.34-3821C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72964677 | |||||||
| chr5:72964742 | C | G | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.34-3756C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72964742 | |||||||
| chr5:72965002 | A | G | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.34-3496A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965002 | |||||||
| chr5:72965136 | A | G | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.34-3362A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965136 | |||||||
| chr5:72965210 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.34-3288A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965210 | |||||||
| chr5:72965230 | T | C | 1 | a0001c0003t0008g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.34-3268T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965230 | |||||||
| chr5:72965635 | A | G | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.34-2863A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965635 | |||||||
| chr5:72965703 | T | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.34-2795T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965703 | |||||||
| chr5:72965855 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.34-2643A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72965855 | |||||||
| chr5:72966199 | G | A | 1 | a0002c0002t0002g0019 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.34-2299G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72966199 | |||||||
| chr5:72966386 | G | A | 88 | a0001c0001t0001g0116 a0001c0001t0001g0144 a0001c0001t0001g0145 others(85): Show |
88 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.34-2112G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72966386 | |||||||
| chr5:72966527 | T | C | 1 | a0001c0001t0015g0166 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.34-1971T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72966527 | |||||||
| chr5:72966655 | T | C | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.34-1843T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72966655 | |||||||
| chr5:72966741 | T | G | 5 | a0001c0003t0005g0233 a0001c0003t0005g0234 a0001c0003t0010g0010 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.34-1757T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72966741 | |||||||
| chr5:72967124 | A | G | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.34-1374A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72967124 | |||||||
| chr5:72967655 | T | A | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.34-843T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72967655 | |||||||
| chr5:72967700 | A | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0223 |
3 | HG00735.hp2 HG01928.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.34-798A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72967700 | |||||||
| chr5:72968003 | C | T | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.34-495C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968003 | |||||||
| chr5:72968053 | T | G | 3 | a0001c0003t0004g0071 a0001c0003t0004g0072 a0001c0003t0004g0073 |
3 | HG01069.hp2 HG01071.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.34-445T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968053 | |||||||
| chr5:72968081 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.34-417C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968081 | |||||||
| chr5:72968114 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.34-384C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968114 | |||||||
| chr5:72968296 | T | C | 1 | a0001c0003t0004g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.34-202T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968296 | |||||||
| chr5:72968337 | A | G | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.34-161A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 1/25 | chr5 | 72968337 | |||||||
| chr5:72968912 | C | G | 2 | a0001c0003t0004g0090 a0005c0011t0004g0089 |
2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.125+323C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72968912 | |||||||
| chr5:72969001 | A | G | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125+412A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72969001 | |||||||
| chr5:72969146 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | NA18998.hp2 NA19001.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.125+557A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72969146 | |||||||
| chr5:72969272 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0214 |
2 | HG00597.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.125+683A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72969272 | |||||||
| chr5:72969340 | T | A | 14 | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0001g0168 others(11): Show |
14 | HG00735.hp2 HG01928.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.125+751T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72969340 | |||||||
| chr5:72970036 | C | T | 6 | a0001c0004t0003g0270 a0001c0004t0003g0271 a0001c0004t0003g0272 others(3): Show |
6 | HG02027.hp2 HG02071.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+1447C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970036 | |||||||
| chr5:72970128 | A | G | 1 | a0001c0004t0003g0275 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.125+1539A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970128 | |||||||
| chr5:72970143 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.125+1554T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970143 | |||||||
| chr5:72970149 | A | G | 1 | a0002c0002t0002g0048 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.125+1560A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970149 | |||||||
| chr5:72970473 | CT | C | 8 | a0001c0001t0001g0215 a0001c0003t0004g0092 a0001c0004t0003g0236 others(5): Show |
8 | HG00621.hp2 HG02523.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.125+1896delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72970473 | ||||||
| chr5:72970585 | T | A | 51 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(48): Show |
51 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.125+1996T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970585 | |||||||
| chr5:72970680 | C | A | 1 | a0002c0002t0002g0015 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.125+2091C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970680 | |||||||
| chr5:72970790 | G | A | 1 | a0002c0002t0002g0113 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.125+2201G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970790 | |||||||
| chr5:72970969 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.125+2380T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970969 | |||||||
| chr5:72970969 | T | C | 5 | a0001c0003t0005g0233 a0001c0003t0005g0234 a0001c0003t0010g0010 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.125+2380T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970969 | |||||||
| chr5:72970978 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.125+2389A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970978 | |||||||
| chr5:72970998 | G | A | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.125+2409G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72970998 | |||||||
| chr5:72971052 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.125+2463A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72971052 | |||||||
| chr5:72971163 | A | G | 4 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0046 others(1): Show |
4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+2574A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72971163 | |||||||
| chr5:72971165 | A | G | 4 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0046 others(1): Show |
4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+2576A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72971165 | |||||||
| chr5:72971289 | G | C | 1 | a0001c0003t0005g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.125+2700G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72971289 | |||||||
| chr5:72971345 | C | T | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.125+2756C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72971345 | |||||||
| chr5:72972022 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0143 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.125+3433A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972022 | |||||||
| chr5:72972075 | G | C | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.125+3486G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972075 | |||||||
| chr5:72972176 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.125+3587C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972176 | |||||||
| chr5:72972177 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.125+3588G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972177 | |||||||
| chr5:72972378 | G | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+3789G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972378 | |||||||
| chr5:72972526 | G | T | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+3937G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972526 | |||||||
| chr5:72972610 | A | G | 1 | a0001c0004t0003g0269 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.125+4021A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972610 | |||||||
| chr5:72972684 | G | A | 97 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(94): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.125+4095G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972684 | |||||||
| chr5:72972703 | T | C | 8 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.125+4114T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972703 | |||||||
| chr5:72972718 | G | T | 44 | a0001c0004t0003g0236 a0001c0004t0003g0237 a0001c0004t0003g0238 others(41): Show |
44 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.125+4129G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972718 | |||||||
| chr5:72972720 | T | C | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.125+4131T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972720 | |||||||
| chr5:72972810 | C | T | 4 | a0001c0003t0005g0233 a0001c0003t0005g0234 a0001c0003t0010g0010 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+4221C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972810 | |||||||
| chr5:72972842 | C | T | 5 | a0001c0004t0003g0236 a0001c0004t0003g0237 a0001c0004t0003g0238 others(2): Show |
5 | HG00621.hp2 HG02523.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+4253C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972842 | |||||||
| chr5:72972880 | A | G | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.125+4291A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72972880 | |||||||
| chr5:72973053 | C | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+4464C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973053 | |||||||
| chr5:72973096 | C | T | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.125+4507C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973096 | |||||||
| chr5:72973185 | C | T | 6 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(3): Show |
6 | HG00642.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+4596C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973185 | |||||||
| chr5:72973186 | A | G | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.125+4597A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973186 | |||||||
| chr5:72973249 | A | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.125+4660A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973249 | |||||||
| chr5:72973293 | G | A | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+4704G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973293 | |||||||
| chr5:72973488 | G | A | 3 | a0001c0001t0001g0165 a0001c0003t0010g0010 a0001c0003t0010g0011 |
3 | HG02615.hp1 HG02630.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.125+4899G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973488 | |||||||
| chr5:72973532 | TG | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0143 |
3 | HG02559.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.125+4946delG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72973532 | ||||||
| chr5:72973538 | C | T | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125+4949C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973538 | |||||||
| chr5:72973572 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.125+4983G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973572 | |||||||
| chr5:72973914 | G | A | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG00438.hp1 NA18747.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.125+5325G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72973914 | |||||||
| chr5:72974191 | T | C | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125+5602T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974191 | |||||||
| chr5:72974241 | C | G | 12 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(9): Show |
12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.125+5652C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974241 | |||||||
| chr5:72974275 | G | A | 12 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(9): Show |
12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.125+5686G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974275 | |||||||
| chr5:72974283 | T | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.125+5694T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974283 | |||||||
| chr5:72974340 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.125+5751G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974340 | |||||||
| chr5:72974448 | T | C | 97 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(94): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.125+5859T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974448 | |||||||
| chr5:72974490 | T | A | 8 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(5): Show |
8 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+5901T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974490 | |||||||
| chr5:72974604 | T | C | 96 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(93): Show |
96 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.125+6015T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974604 | |||||||
| chr5:72974620 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125+6031T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974620 | |||||||
| chr5:72974683 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.125+6094G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974683 | |||||||
| chr5:72974716 | G | A | 3 | a0001c0003t0010g0010 a0001c0003t0010g0011 a0001c0003t0011g0231 |
3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.125+6127G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974716 | |||||||
| chr5:72974719 | G | T | 50 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(47): Show |
50 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.125+6130G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974719 | |||||||
| chr5:72974761 | G | T | 5 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+6172G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974761 | |||||||
| chr5:72974875 | G | A | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.125+6286G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974875 | |||||||
| chr5:72974885 | G | T | 53 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(50): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.125+6296G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974885 | |||||||
| chr5:72974908 | A | C | 2 | a0002c0002t0002g0044 a0002c0002t0002g0045 |
2 | NA18964.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.125+6319A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974908 | |||||||
| chr5:72974955 | A | G | 8 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.125+6366A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974955 | |||||||
| chr5:72974989 | C | T | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.125+6400C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974989 | |||||||
| chr5:72974990 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.125+6401G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974990 | |||||||
| chr5:72974990 | G | T | 5 | a0001c0003t0003g0276 a0001c0003t0003g0277 a0002c0002t0002g0017 others(2): Show |
5 | HG00544.hp2 HG00597.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+6401G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72974990 | |||||||
| chr5:72975238 | G | T | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+6649G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975238 | |||||||
| chr5:72975429 | C | T | 1 | a0001c0004t0003g0266 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.125+6840C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975429 | |||||||
| chr5:72975470 | C | T | 1 | a0001c0004t0003g0266 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.125+6881C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975470 | |||||||
| chr5:72975487 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.125+6898C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975487 | |||||||
| chr5:72975568 | G | A | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+6979G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975568 | |||||||
| chr5:72975631 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.125+7042A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975631 | |||||||
| chr5:72975683 | T | C | 5 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0001c0003t0010g0010 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+7094T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975683 | |||||||
| chr5:72975797 | G | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.125+7208G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975797 | |||||||
| chr5:72975900 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.125+7311A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975900 | |||||||
| chr5:72975946 | G | A | 1 | a0001c0003t0004g0097 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.125+7357G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72975946 | |||||||
| chr5:72976094 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG02040.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.125+7505A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976094 | |||||||
| chr5:72976119 | C | T | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.125+7530C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976119 | |||||||
| chr5:72976266 | G | A | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.125+7677G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976266 | |||||||
| chr5:72976285 | C | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.125+7696C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976285 | |||||||
| chr5:72976298 | C | T | 10 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(7): Show |
10 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+7709C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976298 | |||||||
| chr5:72976299 | G | A | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.125+7710G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976299 | |||||||
| chr5:72976519 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.125+7930C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976519 | |||||||
| chr5:72976625 | T | A | 2 | a0001c0003t0003g0276 a0001c0003t0003g0277 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.125+8036T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976625 | |||||||
| chr5:72976626 | A | T | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125+8037A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976626 | |||||||
| chr5:72976667 | G | A | 52 | a0001c0003t0003g0276 a0001c0003t0003g0277 a0001c0003t0003g0278 others(49): Show |
52 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.125+8078G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976667 | |||||||
| chr5:72976686 | A | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.125+8097A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976686 | |||||||
| chr5:72976713 | G | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+8124G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976713 | |||||||
| chr5:72976885 | G | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125+8296G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976885 | |||||||
| chr5:72976976 | G | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.125+8387G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72976976 | |||||||
| chr5:72977144 | A | T | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.125+8555A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72977144 | |||||||
| chr5:72977239 | C | G | 10 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+8650C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72977239 | |||||||
| chr5:72977658 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.125+9069A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72977658 | |||||||
| chr5:72978001 | A | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.125+9412A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978001 | |||||||
| chr5:72978023 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.125+9434A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978023 | |||||||
| chr5:72978209 | A | G | 1 | a0002c0002t0002g0112 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.125+9620A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978209 | |||||||
| chr5:72978299 | A | G | 12 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(9): Show |
12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.125+9710A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978299 | |||||||
| chr5:72978891 | G | T | 7 | a0001c0004t0003g0261 a0001c0004t0003g0262 a0001c0004t0003g0263 others(4): Show |
7 | HG00558.hp2 HG00609.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.125+10302G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978891 | |||||||
| chr5:72978897 | G | A | 1 | a0001c0009t0001g0126 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.125+10308G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978897 | |||||||
| chr5:72978923 | G | A | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.125+10334G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72978923 | |||||||
| chr5:72978977 | TA | T | 53 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(50): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.125+10390delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72978977 | ||||||
| chr5:72979000 | A | G | 12 | a0002c0002t0002g0049 a0002c0002t0002g0050 a0002c0002t0002g0051 others(9): Show |
12 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.125+10411A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979000 | |||||||
| chr5:72979004 | G | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.125+10415G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979004 | |||||||
| chr5:72979319 | C | T | 3 | a0001c0003t0010g0010 a0001c0003t0010g0011 a0001c0003t0011g0231 |
3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-10108C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979319 | |||||||
| chr5:72979354 | A | G | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.126-10073A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979354 | |||||||
| chr5:72979378 | C | CT | 63 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0119 others(60): Show |
63 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.126-10018dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | ||||||
| chr5:72979378 | C | CTT | 39 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(36): Show |
39 | HG00438.hp1 HG00735.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.126-10019_126-1001 others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | ||||||
| chr5:72979378 | C | CTTT | 23 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0154 others(20): Show |
23 | HG00544.hp1 HG00597.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.126-10020_126-1001 others(7): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | ||||||
| chr5:72979378 | C | CTTTT | 9 | a0001c0001t0001g0116 a0001c0001t0001g0132 a0001c0001t0001g0153 others(6): Show |
9 | HG01258.hp2 HG01884.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.126-10021_126-1001 others(8): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | ||||||
| chr5:72979378 | CT | C | 48 | a0001c0003t0003g0098 a0001c0003t0003g0276 a0001c0003t0003g0277 others(45): Show |
48 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.126-10018delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | ||||||
| chr5:72979378 | CTT | C | 39 | a0001c0001t0015g0166 a0001c0003t0004g0070 a0001c0003t0004g0071 others(36): Show |
39 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.126-10019_126-1001 others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | ||||||
| chr5:72979378 | CTTTTTTT others(3): Show |
C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-10027_126-1001 others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72979378 | ||||||
| chr5:72979392 | T | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-10035T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979392 | |||||||
| chr5:72979393 | T | C | 1 | a0001c0003t0005g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.126-10034T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979393 | |||||||
| chr5:72979394 | T | C | 1 | a0001c0003t0005g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126-10033T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979394 | |||||||
| chr5:72979442 | A | G | 1 | a0001c0003t0010g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.126-9985A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979442 | |||||||
| chr5:72979452 | C | T | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126-9975C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979452 | |||||||
| chr5:72979455 | G | A | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-9972G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979455 | |||||||
| chr5:72979460 | C | T | 50 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(47): Show |
50 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.126-9967C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979460 | |||||||
| chr5:72979537 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.126-9890G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979537 | |||||||
| chr5:72979686 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.126-9741C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979686 | |||||||
| chr5:72979733 | G | A | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.126-9694G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979733 | |||||||
| chr5:72979777 | G | T | 3 | a0002c0002t0002g0016 a0002c0002t0002g0022 a0002c0002t0002g0063 |
3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.126-9650G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979777 | |||||||
| chr5:72979795 | C | G | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.126-9632C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72979795 | |||||||
| chr5:72980190 | C | A | 97 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(94): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.126-9237C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980190 | |||||||
| chr5:72980272 | T | A | 97 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(94): Show |
97 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.126-9155T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980272 | |||||||
| chr5:72980684 | C | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-8743C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980684 | |||||||
| chr5:72980685 | C | G | 3 | a0002c0002t0002g0016 a0002c0002t0002g0022 a0002c0002t0002g0063 |
3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.126-8742C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980685 | |||||||
| chr5:72980711 | C | T | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126-8716C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980711 | |||||||
| chr5:72980794 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126-8633T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980794 | |||||||
| chr5:72980849 | G | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-8578G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980849 | |||||||
| chr5:72980946 | T | A | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-8481T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72980946 | |||||||
| chr5:72981295 | G | GT | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.126-8129dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72981295 | ||||||
| chr5:72981310 | T | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0137 |
3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.126-8117T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981310 | |||||||
| chr5:72981598 | C | T | 1 | a0001c0004t0003g0269 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.126-7829C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981598 | |||||||
| chr5:72981599 | G | A | 4 | a0001c0003t0004g0085 a0001c0003t0004g0086 a0001c0003t0004g0097 others(1): Show |
4 | HG00099.hp1 HG01106.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-7828G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981599 | |||||||
| chr5:72981627 | G | C | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-7800G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981627 | |||||||
| chr5:72981733 | G | A | 46 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0001c0004t0003g0236 others(43): Show |
46 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.126-7694G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981733 | |||||||
| chr5:72981742 | A | G | 12 | a0002c0002t0002g0049 a0002c0002t0002g0050 a0002c0002t0002g0051 others(9): Show |
12 | HG01243.hp2 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.126-7685A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981742 | |||||||
| chr5:72981809 | T | C | 1 | a0005c0011t0004g0089 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.126-7618T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981809 | |||||||
| chr5:72981897 | C | A | 116 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(113): Show |
116 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.126-7530C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981897 | |||||||
| chr5:72981992 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.126-7435G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72981992 | |||||||
| chr5:72982040 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0060 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.126-7387G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982040 | |||||||
| chr5:72982069 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.126-7358C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982069 | |||||||
| chr5:72982081 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.126-7346A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982081 | |||||||
| chr5:72982095 | G | A | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-7332G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982095 | |||||||
| chr5:72982127 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | NA18998.hp2 NA19001.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.126-7300C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982127 | |||||||
| chr5:72982206 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.126-7221C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982206 | |||||||
| chr5:72982332 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.126-7095G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982332 | |||||||
| chr5:72982380 | T | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-7047T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982380 | |||||||
| chr5:72982723 | T | C | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126-6704T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982723 | |||||||
| chr5:72982762 | A | C | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.126-6665A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982762 | |||||||
| chr5:72982822 | A | T | 2 | a0002c0002t0002g0016 a0002c0002t0002g0063 |
2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.126-6605A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982822 | |||||||
| chr5:72982826 | AT | A | 18 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0139 others(15): Show |
18 | HG00558.hp1 HG02074.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.126-6581delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72982826 | ||||||
| chr5:72982826 | ATT | A | 196 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(193): Show |
196 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.126-6582_126-6581d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72982826 | ||||||
| chr5:72982931 | TCAGA | T | 23 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(20): Show |
23 | HG00597.hp2 HG01070.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.126-6491_126-6488d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72982931 | ||||||
| chr5:72982974 | C | T | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.126-6453C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72982974 | |||||||
| chr5:72983037 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0226 |
2 | HG01978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.126-6390C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983037 | |||||||
| chr5:72983062 | C | T | 3 | a0001c0003t0004g0080 a0001c0003t0004g0094 a0002c0002t0002g0059 |
3 | HG00423.hp1 HG00609.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.126-6365C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983062 | |||||||
| chr5:72983080 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.126-6347A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983080 | |||||||
| chr5:72983126 | A | T | 1 | a0002c0002t0002g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.126-6301A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983126 | |||||||
| chr5:72983209 | C | G | 46 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0151 others(43): Show |
46 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.126-6218C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983209 | |||||||
| chr5:72983236 | C | T | 1 | a0002c0002t0002g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.126-6191C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983236 | |||||||
| chr5:72983335 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.126-6092G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983335 | |||||||
| chr5:72983336 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.126-6091G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983336 | |||||||
| chr5:72983482 | G | C | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-5945G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983482 | |||||||
| chr5:72983547 | C | CT | 12 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0176 others(9): Show |
12 | HG01243.hp1 HG02074.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.126-5858dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72983547 | ||||||
| chr5:72983547 | CT | C | 12 | a0001c0001t0001g0165 a0001c0001t0001g0212 a0001c0003t0004g0080 others(9): Show |
12 | HG00423.hp1 HG00609.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.126-5858delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72983547 | ||||||
| chr5:72983704 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.126-5723C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983704 | |||||||
| chr5:72983733 | A | C | 6 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-5694A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983733 | |||||||
| chr5:72983810 | T | A | 3 | a0001c0003t0010g0010 a0001c0003t0010g0011 a0001c0003t0011g0231 |
3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-5617T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983810 | |||||||
| chr5:72983886 | A | G | 1 | a0001c0003t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126-5541A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983886 | |||||||
| chr5:72983990 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.126-5437A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72983990 | |||||||
| chr5:72984117 | T | G | 2 | a0002c0002t0002g0001 a0002c0002t0002g0023 |
3 | HG01070.hp2 HG01071.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.126-5310T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984117 | |||||||
| chr5:72984210 | C | T | 1 | a0002c0002t0002g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.126-5217C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984210 | |||||||
| chr5:72984348 | CT | C | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-5078delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984348 | |||||||
| chr5:72984521 | A | G | 5 | a0001c0003t0005g0233 a0001c0003t0005g0234 a0001c0003t0010g0010 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-4906A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984521 | |||||||
| chr5:72984577 | A | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-4850A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984577 | |||||||
| chr5:72984937 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.126-4490A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72984937 | |||||||
| chr5:72985258 | T | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0137 |
3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.126-4169T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72985258 | |||||||
| chr5:72985286 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.126-4141C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72985286 | |||||||
| chr5:72985287 | G | A | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.126-4140G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72985287 | |||||||
| chr5:72985488 | T | A | 115 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(112): Show |
115 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.126-3939T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72985488 | |||||||
| chr5:72985902 | T | C | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.126-3525T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72985902 | |||||||
| chr5:72986131 | A | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-3296A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986131 | |||||||
| chr5:72986240 | AT | A | 212 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(209): Show |
212 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.126-3177delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72986240 | ||||||
| chr5:72986254 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.126-3173T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986254 | |||||||
| chr5:72986259 | C | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-3168C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986259 | |||||||
| chr5:72986347 | A | G | 1 | a0002c0002t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126-3080A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986347 | |||||||
| chr5:72986418 | A | G | 4 | a0001c0003t0004g0085 a0001c0003t0004g0086 a0001c0003t0004g0097 others(1): Show |
4 | HG00099.hp1 HG01106.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-3009A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986418 | |||||||
| chr5:72986626 | A | T | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126-2801A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986626 | |||||||
| chr5:72986640 | A | G | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.126-2787A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986640 | |||||||
| chr5:72986823 | A | G | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.126-2604A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72986823 | |||||||
| chr5:72986885 | C | CT | 10 | a0001c0001t0001g0174 a0001c0004t0003g0259 a0002c0002t0002g0049 others(7): Show |
10 | HG01884.hp2 HG02809.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-2530dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72986885 | ||||||
| chr5:72987153 | G | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-2274G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72987153 | |||||||
| chr5:72987171 | C | T | 1 | a0002c0002t0002g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.126-2256C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72987171 | |||||||
| chr5:72987412 | A | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126-2015A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72987412 | |||||||
| chr5:72987460 | T | C | 16 | a0001c0003t0005g0003 a0001c0003t0005g0104 a0001c0003t0005g0105 others(13): Show |
16 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-1967T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72987460 | |||||||
| chr5:72987628 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0197 |
2 | NA18947.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.126-1799G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72987628 | |||||||
| chr5:72988109 | C | G | 11 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(8): Show |
11 | HG00642.hp2 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.126-1318C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988109 | |||||||
| chr5:72988166 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.126-1261G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988166 | |||||||
| chr5:72988392 | T | C | 216 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(213): Show |
216 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.126-1035T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988392 | |||||||
| chr5:72988393 | G | T | 1 | a0001c0001t0001g0175 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.126-1034G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988393 | |||||||
| chr5:72988742 | A | C | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.126-685A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988742 | |||||||
| chr5:72988776 | GAATT | G | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126-649_126-646del others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 72988776 | ||||||
| chr5:72988791 | A | G | 5 | a0001c0004t0003g0270 a0001c0004t0003g0271 a0001c0004t0003g0272 others(2): Show |
5 | HG02027.hp2 HG02071.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-636A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988791 | |||||||
| chr5:72988856 | G | T | 1 | a0001c0001t0007g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.126-571G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988856 | |||||||
| chr5:72988986 | A | G | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.126-441A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72988986 | |||||||
| chr5:72989012 | T | C | 14 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(11): Show |
14 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.126-415T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72989012 | |||||||
| chr5:72989026 | T | G | 4 | a0002c0002t0002g0035 a0002c0002t0002g0044 a0002c0002t0002g0045 others(1): Show |
4 | NA18964.hp2 NA18994.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-401T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72989026 | |||||||
| chr5:72989339 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.126-88G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 2/25 | chr5 | 72989339 | |||||||
| chr5:72989594 | T | C | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.200+93T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72989594 | |||||||
| chr5:72989705 | A | C | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.200+204A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72989705 | |||||||
| chr5:72989880 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.200+379T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72989880 | |||||||
| chr5:72989921 | T | C | 4 | a0001c0003t0005g0233 a0001c0003t0005g0234 a0001c0003t0010g0010 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.200+420T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72989921 | |||||||
| chr5:72990057 | G | C | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.201-421G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72990057 | |||||||
| chr5:72990159 | TAG | T | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.201-317_201-316del others(2): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr5 | 72990159 | ||||||
| chr5:72990387 | A | G | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.201-91A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 3/25 | chr5 | 72990387 | |||||||
| chr5:72990657 | G | C | 3 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 |
3 | HG02572.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.342+38G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 4/25 | chr5 | 72990657 | |||||||
| chr5:72991126 | G | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+262G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991126 | |||||||
| chr5:72991153 | C | G | 53 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(50): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.495+289C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991153 | |||||||
| chr5:72991220 | A | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+356A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991220 | |||||||
| chr5:72991250 | G | C | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.495+386G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991250 | |||||||
| chr5:72991280 | T | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+416T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991280 | |||||||
| chr5:72991341 | G | C | 6 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(3): Show |
6 | HG00597.hp2 HG02040.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+477G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991341 | |||||||
| chr5:72991353 | T | C | 5 | a0001c0003t0005g0233 a0001c0003t0005g0234 a0001c0003t0010g0010 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+489T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991353 | |||||||
| chr5:72991444 | G | A | 1 | a0001c0004t0003g0270 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.495+580G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991444 | |||||||
| chr5:72991801 | A | C | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.495+937A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72991801 | |||||||
| chr5:72992903 | T | A | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+2039T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72992903 | |||||||
| chr5:72992903 | T | G | 4 | a0002c0002t0002g0035 a0002c0002t0002g0044 a0002c0002t0002g0045 others(1): Show |
4 | NA18964.hp2 NA18994.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+2039T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72992903 | |||||||
| chr5:72992965 | TA | T | 53 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(50): Show |
53 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.495+2113delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72992965 | ||||||
| chr5:72992986 | C | T | 1 | a0002c0002t0002g0039 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.495+2122C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72992986 | |||||||
| chr5:72993264 | T | G | 1 | a0001c0004t0003g0241 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.495+2400T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993264 | |||||||
| chr5:72993591 | C | A | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.495+2727C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993591 | |||||||
| chr5:72993694 | G | A | 50 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(47): Show |
50 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.495+2830G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993694 | |||||||
| chr5:72993780 | T | A | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.495+2916T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993780 | |||||||
| chr5:72993844 | G | T | 213 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(210): Show |
213 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.495+2980G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993844 | |||||||
| chr5:72993902 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.495+3038A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72993902 | |||||||
| chr5:72994024 | A | G | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.495+3160A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994024 | |||||||
| chr5:72994078 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.495+3214A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994078 | |||||||
| chr5:72994155 | T | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0022 a0002c0002t0002g0063 |
3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.495+3291T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994155 | |||||||
| chr5:72994265 | A | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.495+3401A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994265 | |||||||
| chr5:72994316 | G | A | 2 | a0001c0003t0004g0083 a0001c0003t0004g0084 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.495+3452G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994316 | |||||||
| chr5:72994508 | G | A | 1 | a0001c0004t0003g0258 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.495+3644G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994508 | |||||||
| chr5:72994559 | G | A | 6 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0019 others(3): Show |
6 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+3695G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994559 | |||||||
| chr5:72994617 | C | A | 1 | a0001c0003t0003g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.495+3753C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994617 | |||||||
| chr5:72994621 | C | A | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+3757C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994621 | |||||||
| chr5:72994634 | A | G | 1 | a0001c0001t0018g0225 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.495+3770A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994634 | |||||||
| chr5:72994696 | A | T | 1 | a0001c0005t0003g0257 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.495+3832A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994696 | |||||||
| chr5:72994800 | A | G | 3 | a0001c0003t0010g0010 a0001c0003t0010g0011 a0001c0003t0011g0231 |
3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.495+3936A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994800 | |||||||
| chr5:72994830 | G | A | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+3966G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994830 | |||||||
| chr5:72994922 | T | G | 10 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.495+4058T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72994922 | |||||||
| chr5:72995004 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.495+4140C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995004 | |||||||
| chr5:72995125 | A | G | 1 | a0001c0001t0007g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.495+4261A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995125 | |||||||
| chr5:72995173 | GAAAT | G | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.495+4312_495+4315d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72995173 | ||||||
| chr5:72995351 | G | A | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.495+4487G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995351 | |||||||
| chr5:72995380 | C | T | 1 | a0001c0003t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.495+4516C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995380 | |||||||
| chr5:72995629 | A | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+4765A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995629 | |||||||
| chr5:72995640 | G | A | 2 | a0001c0003t0011g0231 a0003c0006t0005g0004 |
2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.495+4776G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995640 | |||||||
| chr5:72995658 | G | C | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.495+4794G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995658 | |||||||
| chr5:72995703 | G | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+4839G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995703 | |||||||
| chr5:72995868 | C | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+5004C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995868 | |||||||
| chr5:72995932 | A | G | 1 | a0001c0003t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.495+5068A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72995932 | |||||||
| chr5:72996230 | C | T | 3 | a0002c0002t0002g0016 a0002c0002t0002g0022 a0002c0002t0002g0063 |
3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.495+5366C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996230 | |||||||
| chr5:72996241 | C | T | 1 | a0001c0004t0003g0236 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.495+5377C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996241 | |||||||
| chr5:72996243 | C | A | 1 | a0001c0004t0003g0236 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.495+5379C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996243 | |||||||
| chr5:72996243 | C | CA | 71 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0122 others(68): Show |
71 | HG00544.hp1 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.495+5396dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | ||||||
| chr5:72996243 | C | CAAAAAAA | 13 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(10): Show |
13 | HG00558.hp2 HG00609.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.495+5390_495+5396d others(9): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | ||||||
| chr5:72996243 | C | CAAAAAAA others(1): Show |
37 | a0001c0003t0003g0280 a0001c0003t0005g0003 a0001c0003t0005g0105 others(34): Show |
37 | HG00621.hp2 HG01081.hp1 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.495+5389_495+5396d others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | ||||||
| chr5:72996243 | C | CAAAAAAA others(2): Show |
12 | a0001c0003t0005g0104 a0001c0003t0005g0106 a0001c0003t0005g0234 others(9): Show |
12 | HG00735.hp1 HG02109.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.495+5388_495+5396d others(11): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | ||||||
| chr5:72996243 | C | CAAAAAAA others(3): Show |
28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+5387_495+5396d others(12): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | ||||||
| chr5:72996243 | C | CAAAAAAA others(4): Show |
4 | a0001c0003t0004g0080 a0001c0003t0004g0093 a0001c0003t0005g0107 others(1): Show |
4 | HG00609.hp2 HG01261.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+5386_495+5396d others(13): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | ||||||
| chr5:72996243 | C | CAAAAAAA others(5): Show |
1 | a0001c0003t0016g0096 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.495+5385_495+5396d others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | ||||||
| chr5:72996243 | C | CAAAAAAA others(6): Show |
1 | a0001c0003t0010g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.495+5384_495+5396d others(15): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72996243 | ||||||
| chr5:72996439 | A | C | 1 | a0001c0003t0008g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.495+5575A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996439 | |||||||
| chr5:72996611 | G | A | 3 | a0001c0001t0001g0183 a0001c0003t0005g0233 a0001c0003t0005g0234 |
3 | HG02622.hp1 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.495+5747G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996611 | |||||||
| chr5:72996726 | C | T | 2 | a0002c0002t0002g0034 a0002c0002t0002g0060 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.495+5862C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996726 | |||||||
| chr5:72996805 | C | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.495+5941C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996805 | |||||||
| chr5:72996847 | C | T | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.495+5983C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996847 | |||||||
| chr5:72996883 | C | T | 30 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0003t0004g0070 others(27): Show |
30 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.495+6019C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72996883 | |||||||
| chr5:72997279 | G | A | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.495+6415G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997279 | |||||||
| chr5:72997315 | G | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03017.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.495+6451G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997315 | |||||||
| chr5:72997573 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.495+6709G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997573 | |||||||
| chr5:72997574 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.495+6710G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997574 | |||||||
| chr5:72997785 | A | G | 3 | a0002c0002t0002g0040 a0002c0002t0002g0064 a0002c0002t0002g0065 |
3 | HG02559.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.495+6921A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997785 | |||||||
| chr5:72997850 | C | T | 1 | a0002c0002t0002g0038 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.495+6986C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72997850 | |||||||
| chr5:72998213 | C | T | 2 | a0002c0002t0002g0016 a0002c0002t0002g0063 |
2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.495+7349C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998213 | |||||||
| chr5:72998343 | C | T | 40 | a0001c0004t0003g0236 a0001c0004t0003g0237 a0001c0004t0003g0238 others(37): Show |
40 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.495+7479C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998343 | |||||||
| chr5:72998345 | G | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+7481G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998345 | |||||||
| chr5:72998466 | A | C | 1 | a0001c0003t0008g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.495+7602A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998466 | |||||||
| chr5:72998631 | A | G | 163 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.495+7767A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998631 | |||||||
| chr5:72998815 | A | G | 1 | a0001c0009t0001g0126 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.496-7630A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998815 | |||||||
| chr5:72998887 | G | A | 1 | a0002c0002t0002g0014 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.496-7558G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72998887 | |||||||
| chr5:72999241 | C | T | 51 | a0001c0001t0001g0191 a0001c0003t0003g0098 a0001c0003t0003g0099 others(48): Show |
51 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.496-7204C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999241 | |||||||
| chr5:72999277 | T | A | 1 | a0002c0002t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496-7168T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999277 | |||||||
| chr5:72999329 | T | C | 2 | a0001c0003t0003g0276 a0001c0003t0003g0277 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.496-7116T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999329 | |||||||
| chr5:72999378 | C | CT | 8 | a0001c0001t0001g0130 a0001c0001t0001g0176 a0001c0001t0001g0191 others(5): Show |
8 | HG01261.hp2 HG02615.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.496-7045dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72999378 | ||||||
| chr5:72999378 | CT | C | 33 | a0001c0001t0001g0161 a0001c0001t0001g0169 a0001c0001t0001g0193 others(30): Show |
33 | HG01081.hp2 HG01169.hp2 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.496-7045delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72999378 | ||||||
| chr5:72999378 | CTT | C | 103 | a0001c0003t0003g0098 a0001c0003t0003g0276 a0001c0003t0003g0278 others(100): Show |
105 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.496-7046_496-7045d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72999378 | ||||||
| chr5:72999531 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
7 | HG00642.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.496-6914C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999531 | |||||||
| chr5:72999623 | T | TA | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-6821dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72999623 | ||||||
| chr5:72999630 | G | A | 1 | a0002c0002t0002g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.496-6815G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999630 | |||||||
| chr5:72999680 | C | A | 1 | a0002c0002t0002g0186 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.496-6765C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999680 | |||||||
| chr5:72999709 | C | CT | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-6734dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 72999709 | ||||||
| chr5:72999717 | G | A | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-6728G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999717 | |||||||
| chr5:72999750 | C | T | 92 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(89): Show |
92 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.496-6695C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999750 | |||||||
| chr5:72999799 | G | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-6646G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999799 | |||||||
| chr5:72999808 | A | G | 3 | a0001c0003t0010g0010 a0001c0003t0010g0011 a0001c0003t0011g0231 |
3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496-6637A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999808 | |||||||
| chr5:72999835 | A | G | 1 | a0002c0002t0002g0059 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.496-6610A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999835 | |||||||
| chr5:72999881 | G | C | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.496-6564G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999881 | |||||||
| chr5:72999932 | G | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496-6513G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 72999932 | |||||||
| chr5:73000183 | A | T | 1 | a0002c0002t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496-6262A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73000183 | |||||||
| chr5:73000189 | C | T | 3 | a0001c0003t0010g0010 a0001c0003t0010g0011 a0001c0003t0011g0231 |
3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496-6256C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73000189 | |||||||
| chr5:73000458 | T | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-5987T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73000458 | |||||||
| chr5:73000471 | T | TA | 16 | a0001c0001t0001g0163 a0001c0001t0001g0177 a0001c0001t0001g0188 others(13): Show |
16 | HG00438.hp1 HG00597.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.496-5951dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73000471 | ||||||
| chr5:73000471 | TA | T | 50 | a0001c0001t0001g0160 a0001c0003t0003g0099 a0001c0003t0003g0276 others(47): Show |
50 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.496-5951delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73000471 | ||||||
| chr5:73000471 | TAA | T | 41 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0001c0004t0003g0236 others(38): Show |
41 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.496-5952_496-5951d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73000471 | ||||||
| chr5:73000546 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.496-5899C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73000546 | |||||||
| chr5:73000558 | T | C | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.496-5887T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73000558 | |||||||
| chr5:73000779 | T | TA | 168 | a0001c0001t0001g0167 a0001c0003t0003g0098 a0001c0003t0003g0099 others(165): Show |
170 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.496-5656dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73000779 | ||||||
| chr5:73001133 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.496-5312A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001133 | |||||||
| chr5:73001202 | G | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-5243G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001202 | |||||||
| chr5:73001245 | A | T | 3 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 |
3 | HG02572.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.496-5200A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001245 | |||||||
| chr5:73001448 | C | CA | 10 | a0001c0001t0001g0130 a0001c0001t0001g0167 a0001c0001t0001g0213 others(7): Show |
10 | HG00735.hp2 HG02027.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.496-4974dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73001448 | ||||||
| chr5:73001448 | CA | C | 90 | a0001c0001t0001g0128 a0001c0001t0001g0161 a0001c0001t0001g0200 others(87): Show |
90 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.496-4974delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73001448 | ||||||
| chr5:73001467 | A | G | 1 | a0002c0002t0002g0037 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.496-4978A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001467 | |||||||
| chr5:73001674 | G | A | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496-4771G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001674 | |||||||
| chr5:73001798 | G | T | 1 | a0001c0001t0001g0156 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.496-4647G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001798 | |||||||
| chr5:73001943 | T | A | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.496-4502T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73001943 | |||||||
| chr5:73002083 | G | T | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.496-4362G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002083 | |||||||
| chr5:73002255 | G | T | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.496-4190G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002255 | |||||||
| chr5:73002306 | A | G | 5 | a0001c0003t0005g0233 a0001c0003t0005g0234 a0001c0003t0010g0010 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-4139A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002306 | |||||||
| chr5:73002429 | A | C | 66 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0005 others(63): Show |
68 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.496-4016A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002429 | |||||||
| chr5:73002802 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.496-3643G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002802 | |||||||
| chr5:73002951 | A | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.496-3494A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73002951 | |||||||
| chr5:73003086 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0215 |
2 | NA18986.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.496-3359C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003086 | |||||||
| chr5:73003117 | A | T | 1 | a0002c0002t0002g0023 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.496-3328A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003117 | |||||||
| chr5:73003212 | C | T | 66 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0005 others(63): Show |
68 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.496-3233C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003212 | |||||||
| chr5:73003358 | G | C | 8 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.496-3087G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003358 | |||||||
| chr5:73003425 | G | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0022 a0002c0002t0002g0063 |
3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.496-3020G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003425 | |||||||
| chr5:73003520 | G | T | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.496-2925G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003520 | |||||||
| chr5:73003908 | C | T | 1 | a0002c0002t0002g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.496-2537C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003908 | |||||||
| chr5:73003920 | C | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-2525C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003920 | |||||||
| chr5:73003949 | G | A | 4 | a0002c0002t0002g0112 a0002c0002t0002g0113 a0002c0002t0002g0114 others(1): Show |
4 | HG01928.hp2 HG02300.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-2496G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73003949 | |||||||
| chr5:73004047 | C | CA | 38 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0144 others(35): Show |
39 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.496-2372dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73004047 | ||||||
| chr5:73004047 | CA | C | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0208 others(6): Show |
9 | HG00099.hp2 HG00558.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.496-2372delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73004047 | ||||||
| chr5:73004096 | C | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.496-2349C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73004096 | |||||||
| chr5:73004393 | A | G | 1 | a0001c0003t0006g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.496-2052A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73004393 | |||||||
| chr5:73004399 | G | C | 1 | a0002c0002t0002g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.496-2046G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73004399 | |||||||
| chr5:73004636 | T | A | 109 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.496-1809T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73004636 | |||||||
| chr5:73004636 | T | TA | 47 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(44): Show |
47 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.496-1801dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73004636 | ||||||
| chr5:73005091 | C | T | 1 | a0002c0002t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496-1354C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73005091 | |||||||
| chr5:73005198 | A | G | 1 | a0001c0003t0004g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.496-1247A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73005198 | |||||||
| chr5:73005710 | T | A | 1 | a0001c0003t0003g0278 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-735T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73005710 | |||||||
| chr5:73005874 | G | A | 6 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(3): Show |
6 | HG00597.hp2 HG02040.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-571G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73005874 | |||||||
| chr5:73005877 | A | C | 1 | a0001c0001t0001g0197 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.496-568A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73005877 | |||||||
| chr5:73006106 | TTC | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.496-334_496-333del others(2): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr5 | 73006106 | ||||||
| chr5:73006409 | G | T | 6 | a0001c0004t0003g0240 a0001c0004t0003g0246 a0001c0004t0003g0248 others(3): Show |
6 | NA18940.hp2 NA18941.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-36G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 5/25 | chr5 | 73006409 | |||||||
| chr5:73006583 | G | C | 3 | a0001c0004t0003g0241 a0001c0004t0003g0283 a0001c0004t0003g0284 |
3 | NA18982.hp2 NA19001.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.600+34G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73006583 | |||||||
| chr5:73006603 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.600+54T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73006603 | |||||||
| chr5:73006697 | G | T | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.600+148G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73006697 | |||||||
| chr5:73006922 | A | G | 1 | a0001c0004t0003g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.600+373A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73006922 | |||||||
| chr5:73006945 | A | G | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+396A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73006945 | |||||||
| chr5:73007189 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.600+640C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73007189 | |||||||
| chr5:73007302 | G | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+753G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73007302 | |||||||
| chr5:73007698 | A | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.600+1149A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73007698 | |||||||
| chr5:73007717 | A | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.600+1168A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73007717 | |||||||
| chr5:73007961 | A | T | 69 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0005 others(66): Show |
71 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.600+1412A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73007961 | |||||||
| chr5:73008241 | G | T | 5 | a0001c0005t0003g0247 a0001c0005t0003g0253 a0001c0005t0003g0256 others(2): Show |
5 | NA18939.hp1 NA18966.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+1692G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73008241 | |||||||
| chr5:73008318 | A | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.600+1769A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73008318 | |||||||
| chr5:73008650 | A | G | 1 | a0001c0004t0003g0275 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.600+2101A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73008650 | |||||||
| chr5:73008984 | A | T | 4 | a0001c0003t0004g0077 a0001c0003t0004g0078 a0001c0003t0004g0082 others(1): Show |
4 | HG00438.hp2 NA18984.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+2435A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73008984 | |||||||
| chr5:73008990 | G | T | 1 | a0001c0001t0001g0155 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.600+2441G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73008990 | |||||||
| chr5:73009093 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.600+2544A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009093 | |||||||
| chr5:73009115 | G | A | 14 | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0001g0168 others(11): Show |
14 | HG00735.hp2 HG01928.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+2566G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009115 | |||||||
| chr5:73009273 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+2724C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009273 | |||||||
| chr5:73009376 | C | T | 164 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(161): Show |
166 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.600+2827C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009376 | |||||||
| chr5:73009710 | T | C | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.600+3161T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009710 | |||||||
| chr5:73009780 | G | C | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.600+3231G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73009780 | |||||||
| chr5:73010019 | A | C | 78 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(75): Show |
80 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.600+3470A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73010019 | |||||||
| chr5:73010407 | T | C | 1 | a0001c0003t0005g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.600+3858T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73010407 | |||||||
| chr5:73010626 | C | T | 10 | a0002c0002t0002g0017 a0002c0002t0002g0018 a0002c0002t0002g0020 others(7): Show |
10 | HG00544.hp2 HG00597.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+4077C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73010626 | |||||||
| chr5:73010746 | G | A | 1 | a0001c0001t0015g0166 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.600+4197G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73010746 | |||||||
| chr5:73010875 | C | CA | 52 | a0001c0001t0001g0117 a0001c0001t0001g0121 a0001c0001t0001g0146 others(49): Show |
52 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.600+4353dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | ||||||
| chr5:73010875 | CA | C | 10 | a0001c0001t0001g0165 a0001c0001t0001g0204 a0001c0001t0001g0212 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+4353delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | ||||||
| chr5:73010875 | CAAAAAAA others(3): Show |
C | 1 | a0001c0003t0005g0104 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.600+4344_600+4353d others(12): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | ||||||
| chr5:73010875 | CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0005g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.600+4343_600+4353d others(13): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | ||||||
| chr5:73010875 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0007g0229 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.600+4342_600+4353d others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | ||||||
| chr5:73010875 | CAAAAAAA others(6): Show |
C | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.600+4341_600+4353d others(15): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73010875 | ||||||
| chr5:73011049 | T | G | 1 | a0002c0002t0002g0048 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.600+4500T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011049 | |||||||
| chr5:73011114 | A | C | 1 | a0002c0002t0002g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.601-4512A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011114 | |||||||
| chr5:73011167 | A | G | 1 | a0001c0004t0003g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.601-4459A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011167 | |||||||
| chr5:73011242 | G | A | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.601-4384G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011242 | |||||||
| chr5:73011315 | G | T | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.601-4311G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011315 | |||||||
| chr5:73011461 | A | AT | 51 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(48): Show |
51 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.601-4156dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73011461 | ||||||
| chr5:73011488 | T | C | 1 | a0001c0003t0004g0082 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.601-4138T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011488 | |||||||
| chr5:73011500 | A | G | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.601-4126A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011500 | |||||||
| chr5:73011523 | A | T | 1 | a0001c0001t0007g0227 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.601-4103A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011523 | |||||||
| chr5:73011802 | G | C | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.601-3824G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011802 | |||||||
| chr5:73011867 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.601-3759G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011867 | |||||||
| chr5:73011896 | C | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.601-3730C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011896 | |||||||
| chr5:73011938 | G | T | 51 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(48): Show |
51 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.601-3688G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73011938 | |||||||
| chr5:73012164 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.601-3462T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012164 | |||||||
| chr5:73012195 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.601-3431C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012195 | |||||||
| chr5:73012204 | A | G | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-3422A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012204 | |||||||
| chr5:73012316 | T | C | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.601-3310T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012316 | |||||||
| chr5:73012334 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.601-3292T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012334 | |||||||
| chr5:73012360 | C | T | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.601-3266C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012360 | |||||||
| chr5:73012617 | C | CA | 10 | a0001c0001t0001g0125 a0001c0001t0001g0138 a0001c0001t0001g0175 others(7): Show |
10 | HG00597.hp2 HG01168.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.601-2988dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73012617 | ||||||
| chr5:73012617 | CA | C | 148 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.601-2988delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73012617 | ||||||
| chr5:73012713 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.601-2913A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012713 | |||||||
| chr5:73012925 | T | C | 51 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(48): Show |
51 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.601-2701T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73012925 | |||||||
| chr5:73013066 | T | A | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.601-2560T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013066 | |||||||
| chr5:73013213 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.601-2413T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013213 | |||||||
| chr5:73013236 | C | T | 1 | a0001c0004t0003g0262 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.601-2390C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013236 | |||||||
| chr5:73013300 | G | C | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.601-2326G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013300 | |||||||
| chr5:73013591 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.601-2035G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013591 | |||||||
| chr5:73013658 | T | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.601-1968T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013658 | |||||||
| chr5:73013670 | C | G | 1 | a0001c0003t0006g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.601-1956C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013670 | |||||||
| chr5:73013681 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0129 |
2 | HG00558.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.601-1945T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013681 | |||||||
| chr5:73013844 | C | G | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.601-1782C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013844 | |||||||
| chr5:73013858 | G | C | 1 | a0002c0002t0002g0018 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.601-1768G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013858 | |||||||
| chr5:73013928 | C | CTGGCCT | 3 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0004c0008t0003g0279 |
3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.601-1697_601-1692d others(8): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73013928 | ||||||
| chr5:73013935 | C | T | 1 | a0002c0002t0002g0112 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.601-1691C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73013935 | |||||||
| chr5:73014098 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.601-1528C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014098 | |||||||
| chr5:73014149 | G | C | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.601-1477G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014149 | |||||||
| chr5:73014159 | G | A | 1 | a0001c0004t0003g0273 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.601-1467G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014159 | |||||||
| chr5:73014258 | T | C | 1 | a0001c0003t0004g0075 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.601-1368T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014258 | |||||||
| chr5:73014287 | C | T | 48 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(45): Show |
48 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.601-1339C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014287 | |||||||
| chr5:73014322 | T | C | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-1304T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014322 | |||||||
| chr5:73014446 | G | A | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.601-1180G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014446 | |||||||
| chr5:73014575 | A | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.601-1051A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014575 | |||||||
| chr5:73014630 | A | G | 1 | a0002c0002t0002g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.601-996A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014630 | |||||||
| chr5:73014763 | G | A | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-863G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014763 | |||||||
| chr5:73014934 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.601-692A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73014934 | |||||||
| chr5:73015071 | G | A | 4 | a0001c0004t0003g0251 a0002c0002t0002g0016 a0002c0002t0002g0022 others(1): Show |
4 | HG02109.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-555G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73015071 | |||||||
| chr5:73015075 | C | CA | 35 | a0001c0001t0001g0130 a0001c0001t0001g0139 a0001c0001t0001g0146 others(32): Show |
35 | HG00735.hp2 HG01069.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.601-529dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73015075 | ||||||
| chr5:73015075 | CAAAAAAA others(4): Show |
C | 1 | a0001c0004t0003g0236 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.601-539_601-529del others(11): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73015075 | ||||||
| chr5:73015231 | G | GGTGTGTA others(3): Show |
1 | a0001c0003t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601-393_601-392ins others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 73015231 | ||||||
| chr5:73015323 | C | T | 1 | a0001c0004t0003g0262 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.601-303C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73015323 | |||||||
| chr5:73015465 | G | A | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-161G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 6/25 | chr5 | 73015465 | |||||||
| chr5:73015771 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.699+47A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73015771 | |||||||
| chr5:73015953 | A | T | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.699+229A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73015953 | |||||||
| chr5:73016292 | TTTAAAAA others(21): Show |
T | 72 | a0001c0001t0001g0152 a0001c0001t0001g0182 a0001c0003t0003g0276 others(69): Show |
74 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.699+605_699+632del others(28): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016292 | ||||||
| chr5:73016301 | T | TATTTTAA others(133): Show |
1 | a0002c0002t0002g0053 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.699+604_699+605ins others(140): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016301 | ||||||
| chr5:73016311 | TGTTTAAA others(189): Show |
T | 2 | a0001c0004t0003g0243 a0001c0004t0003g0249 |
2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.699+605_700-688del | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016311 | ||||||
| chr5:73016329 | T | G | 8 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0001g0217 others(5): Show |
8 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.699+605T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016329 | |||||||
| chr5:73016329 | T | TATTTTAA others(21): Show |
1 | a0001c0001t0001g0185 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.700-733_700-706dup others(28): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016329 | ||||||
| chr5:73016329 | T | TATTTTAA others(77): Show |
1 | a0001c0001t0001g0207 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.699+699_700-706dup others(84): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016329 | ||||||
| chr5:73016357 | G | T | 37 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0004g0070 others(34): Show |
37 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.699+633G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016357 | |||||||
| chr5:73016367 | TGTTTAAA others(133): Show |
T | 1 | a0001c0001t0001g0128 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.700-705_700-566del | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016367 | ||||||
| chr5:73016385 | G | T | 3 | a0001c0003t0004g0091 a0001c0003t0010g0010 a0001c0003t0010g0011 |
3 | HG02615.hp1 HG02630.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.699+661G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016385 | |||||||
| chr5:73016395 | TGTTTAAA others(105): Show |
T | 3 | a0001c0003t0005g0233 a0001c0003t0005g0234 a0001c0003t0011g0231 |
3 | HG02280.hp2 HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.700-705_700-594del | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016395 | ||||||
| chr5:73016413 | G | T | 4 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0010g0010 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+689G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016413 | |||||||
| chr5:73016423 | TGTTTAAA others(77): Show |
T | 8 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0008g0109 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.700-705_700-622del others(84): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016423 | ||||||
| chr5:73016451 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.699+727T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016451 | |||||||
| chr5:73016451 | TGTTTAAA others(49): Show |
T | 59 | a0001c0003t0003g0276 a0001c0003t0003g0277 a0001c0003t0003g0278 others(56): Show |
59 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.700-705_700-650del others(56): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016451 | ||||||
| chr5:73016479 | TGTTTAAA others(21): Show |
T | 21 | a0001c0001t0001g0129 a0001c0001t0001g0158 a0001c0001t0001g0159 others(18): Show |
21 | HG00621.hp1 HG01069.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.700-705_700-678del others(28): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 73016479 | ||||||
| chr5:73016507 | A | T | 166 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.700-705A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016507 | |||||||
| chr5:73016525 | G | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.700-687G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73016525 | |||||||
| chr5:73017000 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.700-212G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73017000 | |||||||
| chr5:73017204 | T | C | 1 | a0001c0003t0006g0103 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.700-8T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 7/25 | chr5 | 73017204 | |||||||
| chr5:73017852 | TG | T | 4 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0046 others(1): Show |
4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+546delG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73017852 | ||||||
| chr5:73018006 | CTATT | C | 4 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG00642.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.796+703_796+706del others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73018006 | ||||||
| chr5:73018041 | T | A | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.796+733T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018041 | |||||||
| chr5:73018047 | T | C | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+739T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018047 | |||||||
| chr5:73018063 | A | T | 40 | a0001c0004t0003g0236 a0001c0004t0003g0237 a0001c0004t0003g0238 others(37): Show |
40 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.796+755A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018063 | |||||||
| chr5:73018298 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02155.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.796+990C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018298 | |||||||
| chr5:73018299 | C | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02155.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.796+991C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018299 | |||||||
| chr5:73018394 | A | G | 1 | a0001c0004t0003g0273 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.796+1086A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018394 | |||||||
| chr5:73018436 | C | CT | 33 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(30): Show |
33 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.796+1128_796+1129i others(3): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018436 | |||||||
| chr5:73018491 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.796+1183C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018491 | |||||||
| chr5:73018526 | T | C | 1 | a0001c0003t0004g0073 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.796+1218T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73018526 | |||||||
| chr5:73019132 | A | G | 6 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0019 others(3): Show |
6 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.796+1824A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019132 | |||||||
| chr5:73019486 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.796+2178A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019486 | |||||||
| chr5:73019501 | A | G | 7 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0003t0005g0104 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+2193A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019501 | |||||||
| chr5:73019623 | C | T | 4 | a0001c0003t0005g0233 a0001c0003t0005g0234 a0001c0003t0010g0010 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+2315C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019623 | |||||||
| chr5:73019663 | C | T | 10 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.796+2355C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019663 | |||||||
| chr5:73019784 | C | G | 1 | a0001c0004t0003g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.796+2476C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019784 | |||||||
| chr5:73019870 | G | T | 1 | a0001c0004t0003g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.796+2562G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019870 | |||||||
| chr5:73019963 | A | G | 14 | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0001g0168 others(11): Show |
14 | HG00735.hp2 HG01928.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.796+2655A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73019963 | |||||||
| chr5:73020031 | A | G | 44 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0003t0004g0070 others(41): Show |
44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.796+2723A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020031 | |||||||
| chr5:73020274 | A | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.796+2966A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020274 | |||||||
| chr5:73020473 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.796+3165C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020473 | |||||||
| chr5:73020610 | G | A | 66 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0005 others(63): Show |
68 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.796+3302G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020610 | |||||||
| chr5:73020774 | T | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+3466T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020774 | |||||||
| chr5:73020975 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.796+3667C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73020975 | |||||||
| chr5:73021092 | G | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+3784G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021092 | |||||||
| chr5:73021326 | C | T | 1 | a0001c0003t0006g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.796+4018C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021326 | |||||||
| chr5:73021410 | A | G | 3 | a0002c0002t0002g0032 a0002c0002t0002g0036 a0002c0002t0002g0058 |
3 | NA18950.hp1 NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.796+4102A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021410 | |||||||
| chr5:73021647 | A | G | 2 | a0001c0003t0004g0080 a0001c0003t0004g0094 |
2 | HG00423.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.796+4339A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021647 | |||||||
| chr5:73021806 | G | T | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.796+4498G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021806 | |||||||
| chr5:73021809 | A | C | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.796+4501A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021809 | |||||||
| chr5:73021883 | A | T | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.796+4575A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021883 | |||||||
| chr5:73021895 | G | A | 24 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0151 others(21): Show |
24 | HG00544.hp1 HG01258.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.796+4587G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73021895 | |||||||
| chr5:73022090 | A | G | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.796+4782A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022090 | |||||||
| chr5:73022214 | T | C | 1 | a0002c0002t0002g0026 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.796+4906T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022214 | |||||||
| chr5:73022418 | T | G | 1 | a0002c0002t0002g0008 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.796+5110T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022418 | |||||||
| chr5:73022475 | G | C | 5 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0003t0005g0106 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.796+5167G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022475 | |||||||
| chr5:73022498 | C | T | 1 | a0006c0007t0003g0267 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.796+5190C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022498 | |||||||
| chr5:73022552 | G | A | 1 | a0001c0004t0009g0281 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.796+5244G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022552 | |||||||
| chr5:73022571 | C | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.796+5263C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022571 | |||||||
| chr5:73022721 | A | T | 6 | a0001c0003t0004g0077 a0001c0003t0004g0078 a0001c0003t0004g0080 others(3): Show |
6 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.796+5413A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73022721 | |||||||
| chr5:73023437 | C | G | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.796+6129C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023437 | |||||||
| chr5:73023559 | G | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+6251G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023559 | |||||||
| chr5:73023625 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0003t0005g0108 |
3 | HG02559.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.796+6317G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023625 | |||||||
| chr5:73023700 | CA | C | 29 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.796+6406delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73023700 | ||||||
| chr5:73023731 | A | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.796+6423A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023731 | |||||||
| chr5:73023789 | G | A | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.796+6481G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023789 | |||||||
| chr5:73023856 | T | G | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.796+6548T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023856 | |||||||
| chr5:73023919 | A | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0137 |
3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.796+6611A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73023919 | |||||||
| chr5:73024095 | T | C | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.796+6787T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024095 | |||||||
| chr5:73024146 | A | T | 1 | a0001c0003t0004g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.796+6838A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024146 | |||||||
| chr5:73024185 | A | G | 100 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0003t0003g0098 others(97): Show |
100 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.796+6877A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024185 | |||||||
| chr5:73024475 | C | T | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.796+7167C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024475 | |||||||
| chr5:73024478 | C | T | 1 | a0002c0002t0002g0039 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.796+7170C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024478 | |||||||
| chr5:73024576 | T | C | 263 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(260): Show |
265 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.796+7268T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024576 | |||||||
| chr5:73024629 | G | T | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.796+7321G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024629 | |||||||
| chr5:73024631 | G | A | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.796+7323G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024631 | |||||||
| chr5:73024731 | G | A | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.796+7423G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024731 | |||||||
| chr5:73024784 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.796+7476A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024784 | |||||||
| chr5:73024967 | A | G | 1 | a0001c0003t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.796+7659A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73024967 | |||||||
| chr5:73025265 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.796+7957A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025265 | |||||||
| chr5:73025351 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
4 | HG01258.hp2 HG02148.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+8043G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025351 | |||||||
| chr5:73025375 | A | AT | 38 | a0001c0001t0001g0137 a0001c0001t0001g0179 a0001c0001t0001g0210 others(35): Show |
38 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.796+8087dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73025375 | ||||||
| chr5:73025375 | AT | A | 46 | a0001c0001t0001g0129 a0001c0003t0003g0277 a0001c0003t0003g0278 others(43): Show |
46 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.796+8087delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73025375 | ||||||
| chr5:73025408 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.796+8100C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025408 | |||||||
| chr5:73025506 | A | G | 1 | a0002c0002t0002g0112 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.796+8198A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025506 | |||||||
| chr5:73025577 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.796+8269C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025577 | |||||||
| chr5:73025628 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.796+8320C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025628 | |||||||
| chr5:73025707 | G | A | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.796+8399G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73025707 | |||||||
| chr5:73026008 | A | AT | 3 | a0002c0002t0002g0016 a0002c0002t0002g0022 a0002c0002t0002g0063 |
3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.797-8648dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73026008 | ||||||
| chr5:73026054 | C | T | 48 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(45): Show |
48 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.797-8603C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026054 | |||||||
| chr5:73026061 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.797-8596C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026061 | |||||||
| chr5:73026082 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.797-8575A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026082 | |||||||
| chr5:73026116 | A | T | 1 | a0001c0001t0001g0216 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.797-8541A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026116 | |||||||
| chr5:73026119 | G | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0022 a0002c0002t0002g0063 |
3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.797-8538G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026119 | |||||||
| chr5:73026554 | A | G | 1 | a0002c0002t0002g0039 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.797-8103A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026554 | |||||||
| chr5:73026631 | C | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.797-8026C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026631 | |||||||
| chr5:73026787 | G | A | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.797-7870G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026787 | |||||||
| chr5:73026911 | C | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.797-7746C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026911 | |||||||
| chr5:73026924 | T | C | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.797-7733T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026924 | |||||||
| chr5:73026939 | G | C | 1 | a0001c0003t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.797-7718G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73026939 | |||||||
| chr5:73027006 | T | G | 2 | a0001c0001t0001g0182 a0001c0004t0003g0273 |
2 | HG01069.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.797-7651T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027006 | |||||||
| chr5:73027021 | T | G | 1 | a0001c0001t0015g0166 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.797-7636T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027021 | |||||||
| chr5:73027021 | T | TG | 4 | a0001c0001t0001g0160 a0001c0001t0001g0206 a0002c0002t0002g0059 others(1): Show |
4 | HG02027.hp1 HG02056.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-7636_797-7635i others(3): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027021 | |||||||
| chr5:73027021 | T | TTG | 6 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(3): Show |
6 | HG00621.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.797-7635_797-7634i others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73027021 | ||||||
| chr5:73027022 | T | G | 63 | a0001c0001t0001g0116 a0001c0001t0001g0138 a0001c0001t0001g0151 others(60): Show |
65 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.797-7635T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027022 | |||||||
| chr5:73027022 | T | TG | 89 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(86): Show |
89 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.797-7635_797-7634i others(3): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027022 | |||||||
| chr5:73027030 | T | G | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-7627T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027030 | |||||||
| chr5:73027037 | T | A | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.797-7620T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027037 | |||||||
| chr5:73027077 | G | A | 1 | a0001c0004t0003g0238 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.797-7580G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027077 | |||||||
| chr5:73027303 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0132 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.797-7354A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027303 | |||||||
| chr5:73027369 | C | CT | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.797-7275dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73027369 | ||||||
| chr5:73027493 | A | G | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.797-7164A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027493 | |||||||
| chr5:73027523 | A | G | 16 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-7134A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027523 | |||||||
| chr5:73027876 | A | G | 10 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG01258.hp1 HG01496.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.797-6781A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027876 | |||||||
| chr5:73027881 | A | T | 95 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(92): Show |
95 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.797-6776A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73027881 | |||||||
| chr5:73028064 | G | A | 1 | a0002c0002t0002g0015 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.797-6593G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73028064 | |||||||
| chr5:73028646 | C | CT | 79 | a0001c0001t0001g0120 a0001c0001t0001g0130 a0001c0001t0001g0151 others(76): Show |
79 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.797-5990dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73028646 | ||||||
| chr5:73028646 | C | CTT | 11 | a0001c0003t0004g0077 a0001c0003t0004g0078 a0001c0003t0004g0080 others(8): Show |
11 | HG00609.hp2 HG02080.hp1 HG03486.hp2 others(8): Show |
intron_variant | MODIFIER | c.797-5991_797-5990d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73028646 | ||||||
| chr5:73028646 | CT | C | 7 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(4): Show |
7 | HG00423.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.797-5990delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73028646 | ||||||
| chr5:73028672 | CA | C | 95 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(92): Show |
95 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.797-5983delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73028672 | ||||||
| chr5:73028816 | A | G | 1 | a0002c0002t0002g0015 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.797-5841A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73028816 | |||||||
| chr5:73029128 | A | C | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-5529A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029128 | |||||||
| chr5:73029468 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.797-5189A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029468 | |||||||
| chr5:73029507 | T | C | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.797-5150T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029507 | |||||||
| chr5:73029544 | A | G | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.797-5113A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029544 | |||||||
| chr5:73029605 | A | C | 3 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0004c0008t0003g0279 |
3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.797-5052A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029605 | |||||||
| chr5:73029999 | T | C | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.797-4658T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73029999 | |||||||
| chr5:73030000 | CTTTTT | C | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.797-4654_797-4650d others(7): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73030000 | ||||||
| chr5:73030044 | T | G | 1 | a0001c0003t0004g0094 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.797-4613T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030044 | |||||||
| chr5:73030045 | G | GT | 44 | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0001g0169 others(41): Show |
44 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.797-4598dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73030045 | ||||||
| chr5:73030045 | G | GTT | 59 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(56): Show |
59 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.797-4599_797-4598d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73030045 | ||||||
| chr5:73030045 | G | T | 1 | a0001c0003t0004g0094 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.797-4612G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030045 | |||||||
| chr5:73030103 | A | G | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.797-4554A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030103 | |||||||
| chr5:73030143 | G | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.797-4514G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030143 | |||||||
| chr5:73030278 | G | A | 1 | a0001c0004t0003g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.797-4379G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030278 | |||||||
| chr5:73030304 | A | G | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.797-4353A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030304 | |||||||
| chr5:73030543 | G | C | 1 | a0002c0002t0002g0019 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.797-4114G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030543 | |||||||
| chr5:73030617 | G | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.797-4040G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030617 | |||||||
| chr5:73030842 | A | C | 2 | a0001c0003t0004g0080 a0001c0003t0004g0094 |
2 | HG00423.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.797-3815A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73030842 | |||||||
| chr5:73031090 | AC | A | 5 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.797-3565delC | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73031090 | ||||||
| chr5:73031212 | T | C | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.797-3445T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031212 | |||||||
| chr5:73031316 | G | T | 1 | a0002c0002t0002g0014 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.797-3341G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031316 | |||||||
| chr5:73031530 | G | C | 2 | a0001c0003t0003g0276 a0001c0003t0003g0277 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.797-3127G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031530 | |||||||
| chr5:73031626 | G | A | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.797-3031G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031626 | |||||||
| chr5:73031674 | A | G | 2 | a0001c0003t0006g0100 a0001c0003t0006g0102 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.797-2983A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031674 | |||||||
| chr5:73031808 | G | A | 2 | a0001c0003t0006g0100 a0001c0003t0006g0102 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.797-2849G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031808 | |||||||
| chr5:73031994 | T | A | 1 | a0001c0001t0007g0227 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.797-2663T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73031994 | |||||||
| chr5:73032233 | G | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | NA18942.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.797-2424G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73032233 | |||||||
| chr5:73032348 | G | T | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.797-2309G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73032348 | |||||||
| chr5:73032880 | AG | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0019g0157 |
3 | NA18939.hp2 NA19060.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.797-1776delG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73032880 | |||||||
| chr5:73032965 | C | T | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.797-1692C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73032965 | |||||||
| chr5:73033057 | G | C | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.797-1600G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033057 | |||||||
| chr5:73033091 | C | A | 1 | a0002c0002t0002g0026 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.797-1566C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033091 | |||||||
| chr5:73033248 | T | C | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.797-1409T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033248 | |||||||
| chr5:73033384 | G | T | 2 | a0001c0004t0003g0273 a0001c0004t0003g0275 |
2 | HG02071.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.797-1273G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033384 | |||||||
| chr5:73033410 | A | T | 1 | a0002c0002t0002g0186 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.797-1247A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033410 | |||||||
| chr5:73033430 | C | T | 16 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.797-1227C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033430 | |||||||
| chr5:73033707 | A | C | 2 | a0001c0003t0004g0092 a0001c0003t0004g0093 |
2 | HG01261.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.797-950A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033707 | |||||||
| chr5:73033885 | T | G | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.797-772T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033885 | |||||||
| chr5:73033894 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.797-763T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033894 | |||||||
| chr5:73033965 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.797-692T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73033965 | |||||||
| chr5:73034062 | A | G | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.797-595A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73034062 | |||||||
| chr5:73034163 | C | T | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.797-494C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73034163 | |||||||
| chr5:73034289 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0137 |
3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.797-368C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73034289 | |||||||
| chr5:73034504 | T | TTAAC | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.797-151_797-150ins others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 73034504 | ||||||
| chr5:73034545 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.797-112G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 8/25 | chr5 | 73034545 | |||||||
| chr5:73034904 | G | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.841+203G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73034904 | |||||||
| chr5:73035200 | T | G | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.841+499T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035200 | |||||||
| chr5:73035302 | C | T | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.841+601C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035302 | |||||||
| chr5:73035305 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.841+604G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035305 | |||||||
| chr5:73035307 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.841+606T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035307 | |||||||
| chr5:73035847 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.841+1146T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035847 | |||||||
| chr5:73035860 | T | C | 66 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0005 others(63): Show |
68 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.841+1159T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035860 | |||||||
| chr5:73035905 | G | A | 40 | a0001c0004t0003g0236 a0001c0004t0003g0237 a0001c0004t0003g0238 others(37): Show |
40 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.841+1204G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035905 | |||||||
| chr5:73035961 | G | A | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.842-1182G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035961 | |||||||
| chr5:73035967 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0137 |
3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.842-1176C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035967 | |||||||
| chr5:73035995 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.842-1148A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73035995 | |||||||
| chr5:73036034 | C | T | 1 | a0002c0002t0002g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.842-1109C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036034 | |||||||
| chr5:73036037 | G | C | 1 | a0001c0003t0004g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.842-1106G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036037 | |||||||
| chr5:73036081 | G | C | 4 | a0001c0003t0004g0085 a0001c0003t0004g0086 a0001c0003t0004g0097 others(1): Show |
4 | HG00099.hp1 HG01106.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.842-1062G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036081 | |||||||
| chr5:73036083 | T | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.842-1060T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036083 | |||||||
| chr5:73036139 | C | T | 1 | a0001c0003t0008g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.842-1004C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036139 | |||||||
| chr5:73036233 | A | T | 60 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0005 others(57): Show |
62 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.842-910A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036233 | |||||||
| chr5:73036478 | A | G | 6 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-665A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036478 | |||||||
| chr5:73036498 | C | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.842-645C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036498 | |||||||
| chr5:73036645 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.842-498G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036645 | |||||||
| chr5:73036667 | C | T | 1 | a0001c0003t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.842-476C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036667 | |||||||
| chr5:73036856 | G | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.842-287G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 9/25 | chr5 | 73036856 | |||||||
| chr5:73037315 | C | CAAAAGTA others(296): Show |
2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.914+114_914+115ins others(303): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | ||||||
| chr5:73037315 | C | CAAAAGTA others(289): Show |
2 | a0001c0003t0003g0278 a0004c0008t0003g0279 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.914+114_914+115ins others(296): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | ||||||
| chr5:73037315 | C | CAAAAGTA others(290): Show |
1 | a0001c0003t0003g0280 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.914+114_914+115ins others(297): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | ||||||
| chr5:73037315 | C | CAAAAGTA others(295): Show |
5 | a0001c0003t0003g0276 a0001c0003t0003g0277 a0001c0003t0008g0110 others(2): Show |
5 | HG03139.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.914+114_914+115ins others(302): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | ||||||
| chr5:73037315 | C | CAAAAGTA others(296): Show |
33 | a0001c0003t0008g0109 a0001c0004t0003g0236 a0001c0004t0003g0237 others(30): Show |
33 | HG00558.hp2 HG00621.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.914+114_914+115ins others(303): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | ||||||
| chr5:73037315 | C | CAAAAGTA others(297): Show |
8 | a0001c0004t0003g0242 a0001c0004t0003g0255 a0001c0004t0003g0263 others(5): Show |
8 | HG00609.hp1 HG00735.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.914+114_914+115ins others(304): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | ||||||
| chr5:73037315 | C | CAAAAGTA others(299): Show |
2 | a0001c0004t0003g0262 a0001c0004t0003g0269 |
2 | HG02080.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.914+114_914+115ins others(306): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | ||||||
| chr5:73037315 | C | CAAAAGTA others(296): Show |
1 | a0001c0004t0003g0243 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.914+114_914+115ins others(303): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73037315 | ||||||
| chr5:73037322 | A | G | 1 | a0002c0002t0002g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.914+107A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73037322 | |||||||
| chr5:73037544 | C | G | 44 | a0001c0004t0003g0236 a0001c0004t0003g0237 a0001c0004t0003g0238 others(41): Show |
44 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.914+329C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73037544 | |||||||
| chr5:73037706 | A | G | 4 | a0001c0001t0007g0227 a0001c0001t0007g0228 a0001c0001t0007g0229 others(1): Show |
4 | HG01081.hp2 HG01496.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.914+491A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73037706 | |||||||
| chr5:73037720 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.914+505A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73037720 | |||||||
| chr5:73037904 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.914+689G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73037904 | |||||||
| chr5:73038150 | TTTTG | T | 4 | a0002c0002t0002g0029 a0002c0002t0002g0040 a0002c0002t0002g0064 others(1): Show |
4 | HG02559.hp1 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+951_914+954del others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73038150 | ||||||
| chr5:73038187 | T | A | 6 | a0001c0004t0003g0240 a0001c0004t0003g0246 a0001c0004t0003g0248 others(3): Show |
6 | NA18940.hp2 NA18941.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.914+972T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038187 | |||||||
| chr5:73038248 | A | G | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.914+1033A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038248 | |||||||
| chr5:73038434 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.914+1219C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038434 | |||||||
| chr5:73038552 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18998.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.914+1337A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038552 | |||||||
| chr5:73038733 | A | G | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+1518A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038733 | |||||||
| chr5:73038758 | C | T | 1 | a0001c0004t0003g0271 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.914+1543C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038758 | |||||||
| chr5:73038765 | C | T | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.914+1550C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73038765 | |||||||
| chr5:73039036 | A | G | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.914+1821A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039036 | |||||||
| chr5:73039320 | A | T | 2 | a0001c0004t0003g0243 a0001c0004t0003g0249 |
2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.915-1971A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039320 | |||||||
| chr5:73039326 | A | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | NA18941.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.915-1965A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039326 | |||||||
| chr5:73039348 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.915-1943A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039348 | |||||||
| chr5:73039452 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.915-1839A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039452 | |||||||
| chr5:73039500 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.915-1791A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039500 | |||||||
| chr5:73039660 | G | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0141 others(1): Show |
4 | NA18942.hp1 NA18990.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.915-1631G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039660 | |||||||
| chr5:73039681 | AT | A | 51 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(48): Show |
51 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.915-1606delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73039681 | ||||||
| chr5:73039812 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
7 | HG00642.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.915-1479C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039812 | |||||||
| chr5:73039864 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.915-1427G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039864 | |||||||
| chr5:73039876 | C | T | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.915-1415C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039876 | |||||||
| chr5:73039881 | C | T | 168 | a0001c0001t0001g0205 a0001c0003t0003g0098 a0001c0003t0003g0099 others(165): Show |
170 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.915-1410C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039881 | |||||||
| chr5:73039918 | TA | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.915-1371delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73039918 | ||||||
| chr5:73039931 | C | T | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.915-1360C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73039931 | |||||||
| chr5:73039954 | AAAG | A | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.915-1328_915-1326d others(5): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr5 | 73039954 | ||||||
| chr5:73040012 | G | A | 1 | a0001c0003t0006g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.915-1279G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73040012 | |||||||
| chr5:73040203 | A | T | 3 | a0001c0004t0003g0241 a0001c0004t0003g0283 a0001c0004t0003g0284 |
3 | NA18982.hp2 NA19001.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.915-1088A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73040203 | |||||||
| chr5:73040591 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0183 |
2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.915-700A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73040591 | |||||||
| chr5:73040792 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.915-499G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73040792 | |||||||
| chr5:73040998 | A | T | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.915-293A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73040998 | |||||||
| chr5:73041043 | T | C | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.915-248T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73041043 | |||||||
| chr5:73041165 | T | A | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.915-126T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73041165 | |||||||
| chr5:73041202 | A | G | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.915-89A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 10/25 | chr5 | 73041202 | |||||||
| chr5:73041517 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.939+202A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041517 | |||||||
| chr5:73041621 | T | C | 3 | a0001c0004t0003g0261 a0001c0004t0003g0265 a0001c0004t0012g0264 |
3 | HG00558.hp2 HG02056.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.939+306T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041621 | |||||||
| chr5:73041736 | C | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.939+421C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041736 | |||||||
| chr5:73041910 | A | G | 6 | a0001c0004t0003g0240 a0001c0004t0003g0246 a0001c0004t0003g0248 others(3): Show |
6 | NA18940.hp2 NA18941.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+595A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041910 | |||||||
| chr5:73041919 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02155.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.939+604A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041919 | |||||||
| chr5:73041937 | G | A | 1 | a0001c0004t0003g0265 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.939+622G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041937 | |||||||
| chr5:73041986 | A | G | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.939+671A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73041986 | |||||||
| chr5:73042024 | C | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.939+709C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042024 | |||||||
| chr5:73042142 | G | A | 1 | a0001c0004t0012g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.939+827G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042142 | |||||||
| chr5:73042143 | G | A | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.939+828G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042143 | |||||||
| chr5:73042216 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02155.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.939+901G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042216 | |||||||
| chr5:73042284 | C | A | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.939+969C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042284 | |||||||
| chr5:73042348 | A | C | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.939+1033A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042348 | |||||||
| chr5:73042642 | T | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.939+1327T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042642 | |||||||
| chr5:73042900 | C | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.939+1585C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042900 | |||||||
| chr5:73042945 | T | C | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.939+1630T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73042945 | |||||||
| chr5:73043106 | CTTTTTTT others(5): Show |
C | 21 | a0001c0001t0001g0116 a0001c0001t0001g0151 a0001c0001t0001g0153 others(18): Show |
21 | HG00544.hp1 HG01258.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.939+1793_939+1804d others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73043106 | ||||||
| chr5:73043154 | C | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.939+1839C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043154 | |||||||
| chr5:73043282 | T | C | 167 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.939+1967T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043282 | |||||||
| chr5:73043283 | G | A | 1 | a0001c0004t0003g0261 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.939+1968G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043283 | |||||||
| chr5:73043336 | A | G | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.939+2021A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043336 | |||||||
| chr5:73043406 | A | T | 1 | a0001c0003t0004g0095 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.939+2091A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043406 | |||||||
| chr5:73043409 | TAC | T | 96 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(93): Show |
96 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.939+2110_939+2111d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73043409 | ||||||
| chr5:73043540 | AATAG | A | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.939+2229_939+2232d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73043540 | ||||||
| chr5:73043725 | G | A | 1 | a0004c0008t0003g0279 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.939+2410G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043725 | |||||||
| chr5:73043749 | G | A | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.939+2434G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043749 | |||||||
| chr5:73043922 | G | T | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.939+2607G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73043922 | |||||||
| chr5:73044251 | C | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.939+2936C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044251 | |||||||
| chr5:73044339 | G | A | 1 | a0001c0004t0003g0263 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.939+3024G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044339 | |||||||
| chr5:73044384 | A | G | 1 | a0001c0003t0004g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.939+3069A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044384 | |||||||
| chr5:73044430 | A | G | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.939+3115A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044430 | |||||||
| chr5:73044598 | A | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.939+3283A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044598 | |||||||
| chr5:73044854 | G | A | 1 | a0002c0002t0002g0232 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.939+3539G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044854 | |||||||
| chr5:73044957 | A | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.939+3642A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73044957 | |||||||
| chr5:73045519 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.939+4204T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73045519 | |||||||
| chr5:73045527 | A | C | 1 | a0002c0002t0002g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+4212A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73045527 | |||||||
| chr5:73045691 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.939+4376A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73045691 | |||||||
| chr5:73046089 | G | C | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.939+4774G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046089 | |||||||
| chr5:73046295 | G | A | 1 | a0002c0002t0002g0006 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.939+4980G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046295 | |||||||
| chr5:73046393 | G | A | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.940-4956G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046393 | |||||||
| chr5:73046864 | A | G | 16 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
16 | HG00558.hp1 HG01168.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.940-4485A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046864 | |||||||
| chr5:73046889 | T | A | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.940-4460T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046889 | |||||||
| chr5:73046972 | G | C | 1 | a0001c0003t0004g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.940-4377G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73046972 | |||||||
| chr5:73047038 | C | A | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.940-4311C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047038 | |||||||
| chr5:73047157 | CTGTT | C | 3 | a0001c0001t0001g0129 a0001c0003t0005g0003 a0003c0006t0005g0004 |
3 | HG02451.hp1 HG02723.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.940-4188_940-4185d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73047157 | ||||||
| chr5:73047159 | G | C | 3 | a0002c0002t0002g0032 a0002c0002t0002g0036 a0002c0002t0002g0058 |
3 | NA18950.hp1 NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.940-4190G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047159 | |||||||
| chr5:73047168 | T | A | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.940-4181T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047168 | |||||||
| chr5:73047209 | C | T | 2 | a0001c0003t0003g0276 a0001c0003t0003g0277 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.940-4140C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047209 | |||||||
| chr5:73047400 | T | G | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0203 |
3 | NA18971.hp2 NA19000.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.940-3949T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047400 | |||||||
| chr5:73047422 | A | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.940-3927A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047422 | |||||||
| chr5:73047562 | C | CT | 7 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0019g0157 others(4): Show |
7 | HG02257.hp1 HG03098.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.940-3773dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73047562 | ||||||
| chr5:73047562 | CT | C | 31 | a0001c0001t0001g0134 a0001c0003t0004g0070 a0001c0003t0004g0071 others(28): Show |
31 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.940-3773delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73047562 | ||||||
| chr5:73047627 | A | G | 1 | a0005c0011t0004g0089 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.940-3722A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73047627 | |||||||
| chr5:73048029 | A | C | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.940-3320A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048029 | |||||||
| chr5:73048050 | C | A | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.940-3299C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048050 | |||||||
| chr5:73048051 | T | G | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.940-3298T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048051 | |||||||
| chr5:73048088 | GC | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.940-3258delC | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73048088 | ||||||
| chr5:73048108 | C | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.940-3241C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048108 | |||||||
| chr5:73048215 | C | T | 1 | a0001c0004t0003g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.940-3134C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048215 | |||||||
| chr5:73048239 | C | T | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.940-3110C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048239 | |||||||
| chr5:73048243 | A | G | 51 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(48): Show |
51 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.940-3106A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048243 | |||||||
| chr5:73048335 | A | C | 2 | a0002c0002t0002g0048 a0002c0002t0002g0186 |
2 | NA18947.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.940-3014A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048335 | |||||||
| chr5:73048479 | A | G | 1 | a0002c0002t0002g0014 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.940-2870A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048479 | |||||||
| chr5:73048781 | TTA | T | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.940-2566_940-2565d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73048781 | ||||||
| chr5:73048833 | C | CTA | 4 | a0001c0001t0001g0151 a0001c0001t0001g0201 a0001c0001t0001g0207 others(1): Show |
4 | HG00544.hp1 NA18973.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-2515_940-2514d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73048833 | ||||||
| chr5:73048843 | A | C | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-2506A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048843 | |||||||
| chr5:73048870 | C | CT | 25 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0121 others(22): Show |
25 | HG00423.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.940-2455dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73048870 | ||||||
| chr5:73048870 | CT | C | 12 | a0001c0001t0001g0187 a0001c0003t0004g0080 a0001c0003t0005g0104 others(9): Show |
12 | HG00609.hp2 HG01169.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.940-2455delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73048870 | ||||||
| chr5:73048969 | C | T | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.940-2380C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73048969 | |||||||
| chr5:73049095 | C | T | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.940-2254C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049095 | |||||||
| chr5:73049127 | C | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.940-2222C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049127 | |||||||
| chr5:73049444 | C | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.940-1905C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049444 | |||||||
| chr5:73049540 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.940-1809C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049540 | |||||||
| chr5:73049682 | T | A | 89 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(86): Show |
89 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.940-1667T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049682 | |||||||
| chr5:73049703 | C | G | 1 | a0001c0003t0003g0278 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.940-1646C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049703 | |||||||
| chr5:73049765 | T | C | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.940-1584T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049765 | |||||||
| chr5:73049936 | T | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.940-1413T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73049936 | |||||||
| chr5:73050144 | A | G | 1 | a0002c0002t0002g0186 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.940-1205A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73050144 | |||||||
| chr5:73050187 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.940-1162C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73050187 | |||||||
| chr5:73050293 | G | GCTAT | 22 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0001c0004t0003g0241 others(19): Show |
22 | HG00735.hp1 HG01081.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.940-1055_940-1052d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050293 | ||||||
| chr5:73050294 | C | CTATCTAT others(1): Show |
18 | a0001c0004t0003g0240 a0001c0004t0003g0246 a0001c0004t0003g0251 others(15): Show |
18 | HG00558.hp2 HG00609.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.940-1052_940-1051i others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | ||||||
| chr5:73050294 | C | CTATCTAT others(5): Show |
3 | a0001c0003t0003g0099 a0001c0003t0003g0276 a0001c0004t0003g0248 |
3 | HG02965.hp2 HG03225.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.940-1052_940-1051i others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | ||||||
| chr5:73050294 | C | CTATCTAT others(9): Show |
2 | a0001c0003t0003g0098 a0001c0003t0003g0277 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.940-1052_940-1051i others(18): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | ||||||
| chr5:73050294 | C | CTATT | 31 | a0001c0001t0001g0118 a0001c0001t0001g0173 a0001c0001t0001g0177 others(28): Show |
31 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.940-1013_940-1010d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | ||||||
| chr5:73050294 | C | CTATTTAT others(1): Show |
20 | a0001c0001t0001g0140 a0001c0001t0001g0150 a0001c0001t0001g0167 others(17): Show |
20 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.940-1017_940-1010d others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | ||||||
| chr5:73050294 | C | CTATTTAT others(5): Show |
1 | a0001c0003t0004g0082 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.940-1021_940-1010d others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | ||||||
| chr5:73050294 | CTATT | C | 8 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(5): Show |
8 | HG02257.hp1 HG02280.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-1013_940-1010d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | ||||||
| chr5:73050294 | CTATTTAT others(1): Show |
C | 7 | a0001c0003t0005g0003 a0001c0003t0005g0104 a0001c0003t0005g0105 others(4): Show |
7 | HG02451.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.940-1017_940-1010d others(10): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | ||||||
| chr5:73050294 | CTATTTAT others(5): Show |
C | 15 | a0001c0001t0001g0116 a0001c0001t0001g0153 a0001c0001t0001g0154 others(12): Show |
15 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.940-1021_940-1010d others(14): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | ||||||
| chr5:73050294 | CTATTTAT others(9): Show |
C | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.940-1025_940-1010d others(18): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050294 | ||||||
| chr5:73050298 | T | C | 6 | a0001c0004t0003g0236 a0001c0004t0003g0237 a0001c0004t0003g0238 others(3): Show |
6 | HG00621.hp2 HG02071.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-1051T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73050298 | |||||||
| chr5:73050302 | T | C | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.940-1047T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73050302 | |||||||
| chr5:73050411 | TG | T | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-935delG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr5 | 73050411 | ||||||
| chr5:73050564 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0183 a0001c0001t0001g0187 |
3 | HG03041.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.940-785G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73050564 | |||||||
| chr5:73051263 | A | T | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.940-86A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73051263 | |||||||
| chr5:73051289 | A | G | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.940-60A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 11/25 | chr5 | 73051289 | |||||||
| chr5:73051516 | A | C | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+110A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73051516 | |||||||
| chr5:73051586 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.997+180A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73051586 | |||||||
| chr5:73051700 | T | G | 167 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.997+294T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73051700 | |||||||
| chr5:73051814 | C | T | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.997+408C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73051814 | |||||||
| chr5:73052084 | G | A | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.998-248G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73052084 | |||||||
| chr5:73052106 | G | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.998-226G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73052106 | |||||||
| chr5:73052203 | G | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.998-129G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 12/25 | chr5 | 73052203 | |||||||
| chr5:73052619 | C | T | 1 | a0001c0003t0004g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1173+112C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73052619 | |||||||
| chr5:73052725 | G | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1173+218G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73052725 | |||||||
| chr5:73053038 | C | T | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+531C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053038 | |||||||
| chr5:73053039 | C | A | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+532C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053039 | |||||||
| chr5:73053040 | A | T | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+533A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053040 | |||||||
| chr5:73053041 | G | A | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+534G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053041 | |||||||
| chr5:73053042 | T | C | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+535T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053042 | |||||||
| chr5:73053044 | A | T | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+537A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053044 | |||||||
| chr5:73053046 | T | G | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+539T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053046 | |||||||
| chr5:73053048 | T | G | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+541T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053048 | |||||||
| chr5:73053049 | T | A | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+542T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053049 | |||||||
| chr5:73053051 | T | G | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+544T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053051 | |||||||
| chr5:73053052 | C | T | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+545C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053052 | |||||||
| chr5:73053053 | C | T | 1 | a0001c0004t0003g0254 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1173+546C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053053 | |||||||
| chr5:73053183 | T | A | 2 | a0002c0002t0002g0012 a0002c0002t0002g0013 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1173+676T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053183 | |||||||
| chr5:73053260 | T | C | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1173+753T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053260 | |||||||
| chr5:73053275 | C | A | 5 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+768C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053275 | |||||||
| chr5:73053305 | TTTTCTTC others(12): Show |
T | 1 | a0002c0002t0002g0015 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1173+804_1173+822d others(21): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr5 | 73053305 | ||||||
| chr5:73053363 | C | T | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1174-797C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053363 | |||||||
| chr5:73053437 | T | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1174-723T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053437 | |||||||
| chr5:73053444 | C | G | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1174-716C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053444 | |||||||
| chr5:73053650 | T | C | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1174-510T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053650 | |||||||
| chr5:73053653 | A | G | 2 | a0001c0003t0003g0276 a0001c0003t0003g0277 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1174-507A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053653 | |||||||
| chr5:73053657 | C | G | 2 | a0001c0004t0003g0243 a0001c0004t0003g0249 |
2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1174-503C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053657 | |||||||
| chr5:73053695 | CA | C | 95 | a0001c0001t0001g0128 a0001c0003t0003g0098 a0001c0003t0003g0099 others(92): Show |
95 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1174-449delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr5 | 73053695 | ||||||
| chr5:73053757 | G | A | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1174-403G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053757 | |||||||
| chr5:73053886 | C | G | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1174-274C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | chr5 | 73053886 | |||||||
| chr5:73053897 | TAA | T | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1174-258_1174-257d others(4): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr5 | 73053897 | ||||||
| chr5:73053915 | TATTA | T | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-241_1174-238d others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr5 | 73053915 | ||||||
| chr5:73054323 | G | A | 5 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185+152G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 14/25 | chr5 | 73054323 | |||||||
| chr5:73054340 | A | T | 1 | a0002c0002t0002g0114 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1185+169A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 14/25 | chr5 | 73054340 | |||||||
| chr5:73054463 | A | T | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1186-62A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 14/25 | chr5 | 73054463 | |||||||
| chr5:73054705 | G | A | 8 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(5): Show |
8 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1210+156G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73054705 | |||||||
| chr5:73054763 | A | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1210+214A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73054763 | |||||||
| chr5:73054961 | T | C | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210+412T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73054961 | |||||||
| chr5:73054969 | G | T | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210+420G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73054969 | |||||||
| chr5:73055040 | A | G | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1210+491A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055040 | |||||||
| chr5:73055235 | C | G | 167 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1210+686C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055235 | |||||||
| chr5:73055353 | T | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1211-712T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055353 | |||||||
| chr5:73055577 | C | T | 2 | a0002c0002t0002g0041 a0002c0002t0002g0055 |
2 | NA18612.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1211-488C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055577 | |||||||
| chr5:73055670 | A | G | 1 | a0001c0003t0004g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1211-395A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055670 | |||||||
| chr5:73055695 | C | T | 1 | a0001c0003t0004g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1211-370C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055695 | |||||||
| chr5:73055706 | C | T | 3 | a0001c0003t0005g0106 a0001c0003t0005g0107 a0001c0003t0005g0108 |
3 | HG02109.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1211-359C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055706 | |||||||
| chr5:73055806 | G | A | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1211-259G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055806 | |||||||
| chr5:73055881 | T | A | 167 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1211-184T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055881 | |||||||
| chr5:73055996 | T | G | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1211-69T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 15/25 | chr5 | 73055996 | |||||||
| chr5:73056255 | C | A | 1 | a0001c0003t0003g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1253+148C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056255 | |||||||
| chr5:73056447 | C | G | 1 | a0001c0003t0005g0107 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1253+340C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056447 | |||||||
| chr5:73056461 | A | G | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1253+354A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056461 | |||||||
| chr5:73056487 | T | C | 281 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(278): Show |
283 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.1253+380T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056487 | |||||||
| chr5:73056884 | T | C | 1 | a0002c0002t0002g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1253+777T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056884 | |||||||
| chr5:73056941 | C | T | 59 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(56): Show |
59 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1253+834C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056941 | |||||||
| chr5:73056945 | C | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG02040.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1253+838C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73056945 | |||||||
| chr5:73057047 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1253+940C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057047 | |||||||
| chr5:73057071 | C | T | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1253+964C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057071 | |||||||
| chr5:73057102 | A | AT | 166 | a0001c0001t0001g0116 a0001c0003t0003g0098 a0001c0003t0003g0099 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1253+1007dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr5 | 73057102 | ||||||
| chr5:73057103 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1253+996T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057103 | |||||||
| chr5:73057220 | C | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1253+1113C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057220 | |||||||
| chr5:73057321 | G | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0132 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1254-1112G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057321 | |||||||
| chr5:73057379 | T | A | 2 | a0001c0003t0003g0276 a0001c0003t0003g0277 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1254-1054T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057379 | |||||||
| chr5:73057481 | T | C | 3 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0004c0008t0003g0279 |
3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1254-952T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057481 | |||||||
| chr5:73057599 | G | A | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1254-834G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73057599 | |||||||
| chr5:73058002 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1254-431T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73058002 | |||||||
| chr5:73058399 | G | A | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1254-34G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 16/25 | chr5 | 73058399 | |||||||
| chr5:73058613 | T | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1345+89T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73058613 | |||||||
| chr5:73058730 | G | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1345+206G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73058730 | |||||||
| chr5:73058776 | C | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1345+252C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73058776 | |||||||
| chr5:73058939 | G | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1345+415G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73058939 | |||||||
| chr5:73059031 | A | C | 2 | a0001c0003t0006g0100 a0001c0003t0006g0102 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1345+507A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059031 | |||||||
| chr5:73059060 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1345+536T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059060 | |||||||
| chr5:73059070 | T | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1345+546T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059070 | |||||||
| chr5:73059107 | TCAAAAAG others(7): Show |
T | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1345+590_1345+603d others(16): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73059107 | ||||||
| chr5:73059247 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1345+723C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059247 | |||||||
| chr5:73059570 | ATTGGTTT | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1345+1049_1345+105 others(11): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73059570 | ||||||
| chr5:73059622 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0197 |
2 | NA18947.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1345+1098A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059622 | |||||||
| chr5:73059768 | T | A | 1 | a0002c0002t0002g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1345+1244T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73059768 | |||||||
| chr5:73060162 | A | G | 1 | a0001c0003t0003g0280 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1345+1638A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73060162 | |||||||
| chr5:73060325 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1345+1801A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73060325 | |||||||
| chr5:73060354 | A | T | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1345+1830A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73060354 | |||||||
| chr5:73060424 | A | G | 1 | a0001c0003t0004g0094 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1345+1900A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73060424 | |||||||
| chr5:73060768 | GTGT | G | 8 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345+2249_1345+225 others(7): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73060768 | ||||||
| chr5:73060963 | A | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0137 |
3 | HG00642.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1345+2439A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73060963 | |||||||
| chr5:73061007 | C | CA | 70 | a0001c0001t0001g0116 a0001c0001t0001g0124 a0001c0001t0001g0129 others(67): Show |
70 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1345+2497dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73061007 | ||||||
| chr5:73061007 | C | CAA | 11 | a0001c0003t0003g0280 a0001c0003t0005g0003 a0001c0003t0005g0106 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1345+2496_1345+249 others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73061007 | ||||||
| chr5:73061007 | C | CAAA | 25 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(22): Show |
25 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.1345+2495_1345+249 others(7): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73061007 | ||||||
| chr5:73061078 | C | A | 276 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(273): Show |
278 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.1345+2554C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061078 | |||||||
| chr5:73061124 | C | G | 1 | a0001c0001t0007g0227 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1345+2600C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061124 | |||||||
| chr5:73061259 | G | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1346-2582G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061259 | |||||||
| chr5:73061493 | C | T | 4 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0046 others(1): Show |
4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-2348C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061493 | |||||||
| chr5:73061612 | A | G | 7 | a0001c0001t0001g0141 a0001c0003t0005g0003 a0001c0003t0006g0100 others(4): Show |
7 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1346-2229A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061612 | |||||||
| chr5:73061690 | A | G | 1 | a0001c0003t0003g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1346-2151A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061690 | |||||||
| chr5:73061821 | G | A | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1346-2020G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061821 | |||||||
| chr5:73061866 | G | C | 1 | a0001c0001t0018g0225 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1346-1975G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061866 | |||||||
| chr5:73061868 | T | A | 1 | a0001c0001t0007g0227 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1346-1973T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061868 | |||||||
| chr5:73061914 | T | C | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1346-1927T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73061914 | |||||||
| chr5:73062027 | G | A | 1 | a0001c0003t0004g0093 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1346-1814G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062027 | |||||||
| chr5:73062051 | C | T | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0165 others(1): Show |
4 | NA18939.hp2 NA18957.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346-1790C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062051 | |||||||
| chr5:73062056 | A | G | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1346-1785A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062056 | |||||||
| chr5:73062303 | A | G | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346-1538A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062303 | |||||||
| chr5:73062427 | G | A | 51 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(48): Show |
51 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1346-1414G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062427 | |||||||
| chr5:73062962 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1346-879A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73062962 | |||||||
| chr5:73063008 | T | A | 1 | a0001c0004t0009g0281 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1346-833T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73063008 | |||||||
| chr5:73063254 | T | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0183 a0001c0001t0001g0187 |
3 | HG03041.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1346-587T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73063254 | |||||||
| chr5:73063369 | A | AT | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1346-471dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 73063369 | ||||||
| chr5:73063596 | G | C | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-245G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73063596 | |||||||
| chr5:73063604 | T | C | 3 | a0001c0004t0003g0258 a0001c0004t0003g0259 a0006c0007t0003g0267 |
3 | NA18954.hp2 NA19005.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1346-237T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 17/25 | chr5 | 73063604 | |||||||
| chr5:73064011 | A | G | 6 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(3): Show |
6 | HG00642.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449+67A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064011 | |||||||
| chr5:73064251 | C | T | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1449+307C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064251 | |||||||
| chr5:73064282 | C | G | 54 | a0001c0003t0003g0276 a0001c0003t0003g0277 a0001c0003t0003g0278 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1449+338C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064282 | |||||||
| chr5:73064538 | A | T | 3 | a0002c0002t0002g0032 a0002c0002t0002g0036 a0002c0002t0002g0058 |
3 | NA18950.hp1 NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1449+594A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064538 | |||||||
| chr5:73064675 | C | T | 1 | a0001c0004t0009g0281 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1449+731C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064675 | |||||||
| chr5:73064706 | C | A | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1449+762C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064706 | |||||||
| chr5:73064848 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1449+904A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064848 | |||||||
| chr5:73064945 | G | C | 1 | a0001c0001t0018g0225 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1449+1001G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064945 | |||||||
| chr5:73064974 | T | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1449+1030T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73064974 | |||||||
| chr5:73065095 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1449+1151G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065095 | |||||||
| chr5:73065168 | G | A | 1 | a0002c0002t0002g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1449+1224G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065168 | |||||||
| chr5:73065257 | T | C | 1 | a0001c0004t0003g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1449+1313T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065257 | |||||||
| chr5:73065290 | A | AT | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1449+1355dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 73065290 | ||||||
| chr5:73065510 | A | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1449+1566A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065510 | |||||||
| chr5:73065624 | T | A | 1 | a0002c0002t0002g0038 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1449+1680T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065624 | |||||||
| chr5:73065805 | C | T | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1449+1861C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065805 | |||||||
| chr5:73065857 | C | T | 1 | a0002c0002t0002g0046 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1449+1913C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73065857 | |||||||
| chr5:73066286 | A | AT | 4 | a0001c0003t0005g0233 a0001c0003t0005g0234 a0001c0003t0010g0010 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1449+2345dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 73066286 | ||||||
| chr5:73066323 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1450-2327A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066323 | |||||||
| chr5:73066462 | A | G | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1450-2188A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066462 | |||||||
| chr5:73066528 | A | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0210 |
3 | HG00642.hp2 HG04184.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1450-2122A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066528 | |||||||
| chr5:73066575 | C | CT | 35 | a0001c0003t0003g0280 a0001c0003t0004g0070 a0001c0003t0004g0071 others(32): Show |
35 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1450-2056dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 73066575 | ||||||
| chr5:73066575 | CT | C | 118 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(115): Show |
118 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.1450-2056delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 73066575 | ||||||
| chr5:73066579 | T | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1450-2071T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066579 | |||||||
| chr5:73066739 | G | C | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1450-1911G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066739 | |||||||
| chr5:73066760 | A | T | 1 | a0002c0002t0002g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1450-1890A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73066760 | |||||||
| chr5:73067102 | G | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1450-1548G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067102 | |||||||
| chr5:73067104 | A | C | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1450-1546A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067104 | |||||||
| chr5:73067107 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0132 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1450-1543A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067107 | |||||||
| chr5:73067170 | C | A | 1 | a0001c0003t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1450-1480C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067170 | |||||||
| chr5:73067235 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1450-1415G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067235 | |||||||
| chr5:73067387 | G | A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0210 |
3 | HG00642.hp2 HG04184.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1450-1263G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067387 | |||||||
| chr5:73067576 | A | G | 1 | a0001c0004t0003g0242 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1450-1074A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067576 | |||||||
| chr5:73067978 | G | A | 1 | a0002c0002t0002g0037 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1450-672G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73067978 | |||||||
| chr5:73068000 | A | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1450-650A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73068000 | |||||||
| chr5:73068227 | T | G | 2 | a0002c0002t0002g0049 a0002c0002t0002g0050 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1450-423T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 18/25 | chr5 | 73068227 | |||||||
| chr5:73068786 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG04115.hp1 | splice_region_variant&intron_variant | LOW | c.1579+7G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068786 | |||||||
| chr5:73068831 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1579+52A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068831 | |||||||
| chr5:73068834 | C | G | 1 | a0002c0002t0002g0031 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1579+55C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068834 | |||||||
| chr5:73068846 | A | G | 115 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(112): Show |
115 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1579+67A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068846 | |||||||
| chr5:73068860 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1579+81G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068860 | |||||||
| chr5:73068980 | A | C | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579+201A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73068980 | |||||||
| chr5:73069037 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1579+258A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069037 | |||||||
| chr5:73069090 | G | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1579+311G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069090 | |||||||
| chr5:73069469 | T | A | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1579+690T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069469 | |||||||
| chr5:73069504 | G | A | 1 | a0001c0004t0003g0238 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1579+725G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069504 | |||||||
| chr5:73069505 | C | T | 115 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(112): Show |
115 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1579+726C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069505 | |||||||
| chr5:73069571 | G | A | 1 | a0001c0003t0006g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1579+792G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069571 | |||||||
| chr5:73069573 | T | C | 1 | a0001c0004t0003g0263 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1579+794T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069573 | |||||||
| chr5:73069628 | G | A | 4 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0046 others(1): Show |
4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1579+849G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069628 | |||||||
| chr5:73069630 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1579+851G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069630 | |||||||
| chr5:73069673 | CCTT | C | 59 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(56): Show |
59 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1579+897_1579+899d others(5): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 73069673 | ||||||
| chr5:73069724 | A | G | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1579+945A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069724 | |||||||
| chr5:73069734 | A | G | 1 | a0001c0003t0004g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1579+955A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73069734 | |||||||
| chr5:73070023 | A | G | 1 | a0002c0002t0002g0048 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1579+1244A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070023 | |||||||
| chr5:73070029 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1579+1250A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070029 | |||||||
| chr5:73070373 | C | T | 1 | a0001c0004t0003g0265 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1579+1594C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070373 | |||||||
| chr5:73070398 | A | AT | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1579+1620dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 73070398 | ||||||
| chr5:73070565 | GT | G | 18 | a0001c0001t0001g0131 a0001c0003t0003g0098 a0001c0003t0003g0099 others(15): Show |
18 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1579+1802delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 73070565 | ||||||
| chr5:73070572 | T | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1579+1793T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070572 | |||||||
| chr5:73070597 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1579+1818T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070597 | |||||||
| chr5:73070763 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1579+1984T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73070763 | |||||||
| chr5:73071044 | A | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1579+2265A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071044 | |||||||
| chr5:73071144 | A | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1579+2365A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071144 | |||||||
| chr5:73071308 | A | T | 1 | a0002c0002t0002g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1579+2529A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071308 | |||||||
| chr5:73071339 | C | T | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1579+2560C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071339 | |||||||
| chr5:73071345 | T | C | 1 | a0001c0003t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1579+2566T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071345 | |||||||
| chr5:73071425 | T | C | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1579+2646T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071425 | |||||||
| chr5:73071512 | A | G | 213 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(210): Show |
213 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.1579+2733A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071512 | |||||||
| chr5:73071729 | C | T | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+2950C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071729 | |||||||
| chr5:73071790 | G | C | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1580-2952G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071790 | |||||||
| chr5:73071892 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1580-2850G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071892 | |||||||
| chr5:73071892 | G | C | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1580-2850G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071892 | |||||||
| chr5:73071911 | G | C | 1 | a0002c0002t0002g0038 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1580-2831G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071911 | |||||||
| chr5:73071918 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1580-2824G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071918 | |||||||
| chr5:73071926 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1580-2816T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071926 | |||||||
| chr5:73071974 | A | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1580-2768A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73071974 | |||||||
| chr5:73072226 | A | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1580-2516A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73072226 | |||||||
| chr5:73072264 | G | A | 2 | a0001c0004t0003g0242 a0001c0004t0003g0245 |
2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1580-2478G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73072264 | |||||||
| chr5:73072468 | A | C | 2 | a0001c0004t0003g0262 a0001c0004t0003g0269 |
2 | HG02080.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1580-2274A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73072468 | |||||||
| chr5:73072554 | A | C | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1580-2188A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73072554 | |||||||
| chr5:73072812 | G | C | 1 | a0001c0001t0001g0189 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1580-1930G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73072812 | |||||||
| chr5:73073118 | T | G | 2 | a0001c0003t0004g0092 a0001c0003t0004g0093 |
2 | HG01261.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1580-1624T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073118 | |||||||
| chr5:73073139 | T | G | 47 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0001c0004t0003g0236 others(44): Show |
47 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1580-1603T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073139 | |||||||
| chr5:73073526 | G | A | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1580-1216G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073526 | |||||||
| chr5:73073650 | A | G | 1 | a0001c0003t0004g0080 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1580-1092A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073650 | |||||||
| chr5:73073705 | T | A | 93 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(90): Show |
93 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1580-1037T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073705 | |||||||
| chr5:73073755 | G | A | 1 | a0002c0002t0002g0039 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1580-987G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073755 | |||||||
| chr5:73073972 | C | T | 4 | a0001c0003t0006g0100 a0001c0003t0006g0101 a0001c0003t0006g0102 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580-770C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073972 | |||||||
| chr5:73073974 | C | T | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1580-768C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073974 | |||||||
| chr5:73073994 | G | A | 1 | a0002c0002t0002g0006 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1580-748G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73073994 | |||||||
| chr5:73074038 | C | G | 13 | a0001c0003t0004g0077 a0001c0003t0004g0078 a0001c0003t0004g0079 others(10): Show |
13 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.1580-704C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074038 | |||||||
| chr5:73074043 | C | T | 81 | a0001c0003t0003g0276 a0001c0003t0003g0277 a0001c0003t0003g0278 others(78): Show |
81 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1580-699C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074043 | |||||||
| chr5:73074166 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1580-576G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074166 | |||||||
| chr5:73074222 | T | C | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1580-520T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074222 | |||||||
| chr5:73074258 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02155.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1580-484A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074258 | |||||||
| chr5:73074578 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1580-164A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074578 | |||||||
| chr5:73074702 | C | A | 15 | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0001g0168 others(12): Show |
15 | HG00735.hp2 HG01192.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.1580-40C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 19/25 | chr5 | 73074702 | |||||||
| chr5:73074918 | C | T | 54 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(51): Show |
54 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1691+65C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73074918 | |||||||
| chr5:73075072 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1691+219A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075072 | |||||||
| chr5:73075146 | G | C | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1691+293G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075146 | |||||||
| chr5:73075318 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0132 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1691+465G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075318 | |||||||
| chr5:73075542 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1691+689T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075542 | |||||||
| chr5:73075704 | C | T | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1691+851C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075704 | |||||||
| chr5:73075745 | A | G | 1 | a0002c0002t0002g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1691+892A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075745 | |||||||
| chr5:73075844 | A | G | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1691+991A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73075844 | |||||||
| chr5:73075900 | A | AG | 93 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(90): Show |
93 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1691+1051dupG | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr5 | 73075900 | ||||||
| chr5:73076046 | T | A | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1691+1193T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076046 | |||||||
| chr5:73076053 | G | C | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1691+1200G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076053 | |||||||
| chr5:73076058 | A | G | 2 | a0002c0002t0002g0001 a0002c0002t0002g0023 |
3 | HG01070.hp2 HG01071.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1691+1205A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076058 | |||||||
| chr5:73076154 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1692-1184C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076154 | |||||||
| chr5:73076157 | G | T | 51 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(48): Show |
51 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1692-1181G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076157 | |||||||
| chr5:73076179 | G | C | 1 | a0001c0005t0003g0247 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1692-1159G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076179 | |||||||
| chr5:73076313 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1692-1025A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076313 | |||||||
| chr5:73076329 | A | G | 1 | a0001c0003t0006g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1692-1009A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076329 | |||||||
| chr5:73076333 | C | A | 2 | a0001c0003t0005g0104 a0001c0003t0005g0105 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1692-1005C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076333 | |||||||
| chr5:73076502 | T | C | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1692-836T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73076502 | |||||||
| chr5:73077034 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1692-304A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73077034 | |||||||
| chr5:73077124 | A | G | 1 | a0001c0003t0006g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1692-214A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73077124 | |||||||
| chr5:73077144 | A | G | 2 | a0001c0004t0003g0243 a0001c0004t0003g0249 |
2 | NA18984.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1692-194A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73077144 | |||||||
| chr5:73077208 | G | C | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1692-130G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73077208 | |||||||
| chr5:73077260 | G | A | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1692-78G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 20/25 | chr5 | 73077260 | |||||||
| chr5:73077529 | G | A | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1847+36G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 21/25 | chr5 | 73077529 | |||||||
| chr5:73077681 | A | G | 4 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0046 others(1): Show |
4 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1847+188A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 21/25 | chr5 | 73077681 | |||||||
| chr5:73077683 | A | AAAAAAC | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1847+193_1847+198d others(8): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 73077683 | ||||||
| chr5:73077687 | A | G | 3 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0004c0008t0003g0279 |
3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1847+194A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 21/25 | chr5 | 73077687 | |||||||
| chr5:73077885 | A | C | 99 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(96): Show |
99 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1848-295A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 21/25 | chr5 | 73077885 | |||||||
| chr5:73078324 | G | A | 1 | a0002c0002t0002g0006 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1980+12G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078324 | |||||||
| chr5:73078463 | G | A | 1 | a0002c0002t0002g0020 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1980+151G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078463 | |||||||
| chr5:73078612 | A | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | NA18612.hp2 NA18947.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1980+300A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078612 | |||||||
| chr5:73078648 | A | G | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1980+336A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078648 | |||||||
| chr5:73078859 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1980+547C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078859 | |||||||
| chr5:73078927 | A | C | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1980+615A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73078927 | |||||||
| chr5:73079052 | A | G | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1980+740A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73079052 | |||||||
| chr5:73079062 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0156 |
2 | HG02080.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1980+750C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73079062 | |||||||
| chr5:73079141 | T | A | 1 | a0001c0003t0004g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1980+829T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73079141 | |||||||
| chr5:73079458 | T | C | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1980+1146T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73079458 | |||||||
| chr5:73079953 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1980+1641A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73079953 | |||||||
| chr5:73080245 | G | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1981-1538G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080245 | |||||||
| chr5:73080306 | T | C | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0141 others(1): Show |
4 | NA18942.hp1 NA18990.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-1477T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080306 | |||||||
| chr5:73080669 | T | TTA | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1981-1113_1981-111 others(6): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 73080669 | ||||||
| chr5:73080806 | G | A | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1981-977G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080806 | |||||||
| chr5:73080881 | C | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
8 | HG00642.hp1 HG01243.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1981-902C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080881 | |||||||
| chr5:73080889 | T | C | 1 | a0001c0003t0005g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1981-894T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080889 | |||||||
| chr5:73080913 | C | T | 2 | a0001c0003t0005g0003 a0003c0006t0005g0004 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1981-870C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080913 | |||||||
| chr5:73080963 | C | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1981-820C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73080963 | |||||||
| chr5:73081021 | G | T | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1981-762G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081021 | |||||||
| chr5:73081031 | G | C | 1 | a0002c0002t0002g0186 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1981-752G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081031 | |||||||
| chr5:73081335 | C | T | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1981-448C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081335 | |||||||
| chr5:73081461 | C | T | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1981-322C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081461 | |||||||
| chr5:73081594 | A | G | 3 | a0002c0002t0002g0016 a0002c0002t0002g0022 a0002c0002t0002g0063 |
3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1981-189A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081594 | |||||||
| chr5:73081775 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | splice_region_variant&intron_variant | LOW | c.1981-8C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 22/25 | chr5 | 73081775 | |||||||
| chr5:73082050 | A | G | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2180+68A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082050 | |||||||
| chr5:73082188 | A | C | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2180+206A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082188 | |||||||
| chr5:73082260 | C | CT | 201 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(198): Show |
201 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.2180+293dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr5 | 73082260 | ||||||
| chr5:73082260 | CT | C | 6 | a0001c0003t0010g0010 a0001c0003t0010g0011 a0002c0002t0002g0029 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2180+293delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr5 | 73082260 | ||||||
| chr5:73082276 | C | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0132 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2180+294C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082276 | |||||||
| chr5:73082292 | A | T | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2180+310A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082292 | |||||||
| chr5:73082293 | T | A | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2180+311T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082293 | |||||||
| chr5:73082294 | A | T | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2180+312A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082294 | |||||||
| chr5:73082433 | C | T | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2181-328C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082433 | |||||||
| chr5:73082435 | C | T | 3 | a0002c0002t0002g0032 a0002c0002t0002g0036 a0002c0002t0002g0058 |
3 | NA18950.hp1 NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2181-326C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 23/25 | chr5 | 73082435 | |||||||
| chr5:73082855 | A | T | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2245+30A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73082855 | |||||||
| chr5:73082876 | AT | A | 95 | a0001c0001t0001g0161 a0001c0001t0001g0198 a0001c0003t0003g0098 others(92): Show |
95 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.2245+67delT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73082876 | ||||||
| chr5:73082896 | A | G | 1 | a0001c0003t0004g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2245+71A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73082896 | |||||||
| chr5:73083009 | G | C | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2245+184G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083009 | |||||||
| chr5:73083021 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2245+196G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083021 | |||||||
| chr5:73083036 | A | G | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2245+211A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083036 | |||||||
| chr5:73083055 | T | G | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2245+230T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083055 | |||||||
| chr5:73083086 | A | G | 9 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2245+261A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083086 | |||||||
| chr5:73083135 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2245+310C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083135 | |||||||
| chr5:73083136 | G | A | 2 | a0001c0003t0003g0098 a0001c0003t0003g0099 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2245+311G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083136 | |||||||
| chr5:73083194 | C | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2245+369C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083194 | |||||||
| chr5:73083391 | T | A | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2245+566T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083391 | |||||||
| chr5:73083440 | T | TAAGAAAC others(304): Show |
1 | a0001c0001t0015g0166 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2245+624_2245+625i others(313): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73083440 | ||||||
| chr5:73083478 | C | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2245+653C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083478 | |||||||
| chr5:73083547 | C | T | 2 | a0001c0003t0005g0106 a0001c0003t0005g0107 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2245+722C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083547 | |||||||
| chr5:73083614 | C | T | 1 | a0001c0003t0011g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2245+789C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083614 | |||||||
| chr5:73083615 | G | C | 1 | a0003c0006t0005g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2245+790G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083615 | |||||||
| chr5:73083619 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2245+794C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083619 | |||||||
| chr5:73083892 | C | CA | 17 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0129 others(14): Show |
17 | HG00642.hp1 HG00642.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.2245+1087dupA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73083892 | ||||||
| chr5:73083892 | CA | C | 91 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(88): Show |
91 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.2245+1087delA | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73083892 | ||||||
| chr5:73083898 | A | T | 1 | a0001c0004t0003g0246 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+1073A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083898 | |||||||
| chr5:73083914 | C | G | 5 | a0001c0003t0005g0104 a0001c0003t0005g0105 a0001c0003t0005g0106 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2245+1089C>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73083914 | |||||||
| chr5:73084127 | T | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0022 a0002c0002t0002g0063 |
3 | HG02109.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2245+1302T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084127 | |||||||
| chr5:73084255 | G | T | 3 | a0001c0001t0001g0130 a0001c0003t0004g0092 a0001c0003t0004g0093 |
3 | HG01261.hp2 HG02615.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2245+1430G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084255 | |||||||
| chr5:73084395 | A | T | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2245+1570A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084395 | |||||||
| chr5:73084411 | A | G | 216 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(213): Show |
216 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.2245+1586A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084411 | |||||||
| chr5:73084486 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2245+1661G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084486 | |||||||
| chr5:73084567 | A | G | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2245+1742A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084567 | |||||||
| chr5:73084575 | A | G | 3 | a0001c0003t0003g0278 a0001c0003t0003g0280 a0004c0008t0003g0279 |
3 | HG02145.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2245+1750A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084575 | |||||||
| chr5:73084702 | G | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2245+1877G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084702 | |||||||
| chr5:73084758 | A | G | 1 | a0002c0002t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2245+1933A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73084758 | |||||||
| chr5:73085099 | C | T | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.2245+2274C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085099 | |||||||
| chr5:73085131 | G | A | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2245+2306G>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085131 | |||||||
| chr5:73085143 | G | C | 3 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 |
3 | HG02257.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2245+2318G>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085143 | |||||||
| chr5:73085194 | C | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0001g0169 others(1): Show |
4 | NA18986.hp2 NA18992.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245+2369C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085194 | |||||||
| chr5:73085273 | C | T | 98 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0276 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2246-2316C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085273 | |||||||
| chr5:73085511 | A | AT | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2246-2076dupT | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085511 | ||||||
| chr5:73085565 | A | C | 28 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(25): Show |
28 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.2246-2024A>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085565 | |||||||
| chr5:73085777 | A | AAAAT | 4 | a0002c0002t0002g0005 a0002c0002t0002g0051 a0002c0002t0002g0061 others(1): Show |
4 | HG01169.hp1 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2246-1765_2246-176 others(8): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | ||||||
| chr5:73085777 | AAAAT | A | 17 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0022 others(14): Show |
17 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.2246-1765_2246-176 others(8): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | ||||||
| chr5:73085777 | AAAATAAA others(1): Show |
A | 9 | a0001c0004t0003g0241 a0002c0002t0002g0008 a0002c0002t0002g0012 others(6): Show |
9 | HG01099.hp1 HG02109.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.2246-1769_2246-176 others(12): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | ||||||
| chr5:73085777 | AAAATAAA others(5): Show |
A | 60 | a0001c0001t0001g0117 a0001c0001t0001g0131 a0001c0001t0001g0132 others(57): Show |
60 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2246-1773_2246-176 others(16): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | ||||||
| chr5:73085777 | AAAATAAA others(9): Show |
A | 112 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0118 others(109): Show |
112 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.2246-1777_2246-176 others(20): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | ||||||
| chr5:73085777 | AAAATAAA others(13): Show |
A | 36 | a0001c0003t0004g0070 a0001c0003t0004g0071 a0001c0003t0004g0072 others(33): Show |
36 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.2246-1781_2246-176 others(24): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | ||||||
| chr5:73085777 | AAAATAAA others(21): Show |
A | 1 | a0001c0001t0001g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2246-1789_2246-176 others(32): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | ||||||
| chr5:73085777 | AAAATAAA others(25): Show |
A | 6 | a0001c0003t0005g0003 a0001c0003t0006g0100 a0001c0003t0006g0101 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2246-1793_2246-176 others(36): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085777 | ||||||
| chr5:73085781 | T | C | 2 | a0002c0002t0002g0034 a0002c0002t0002g0060 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2246-1808T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085781 | |||||||
| chr5:73085783 | AATAAATA others(11): Show |
A | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1804_2246-178 others(22): Show |
FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr5 | 73085783 | ||||||
| chr5:73085802 | A | T | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1787A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085802 | |||||||
| chr5:73085818 | A | T | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1771A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085818 | |||||||
| chr5:73085972 | A | G | 2 | a0001c0003t0010g0010 a0001c0003t0010g0011 |
2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2246-1617A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73085972 | |||||||
| chr5:73086040 | T | G | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1549T>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086040 | |||||||
| chr5:73086095 | C | T | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1494C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086095 | |||||||
| chr5:73086096 | T | A | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-1493T>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086096 | |||||||
| chr5:73086138 | C | A | 1 | a0001c0009t0001g0126 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2246-1451C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086138 | |||||||
| chr5:73086608 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2246-981C>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086608 | |||||||
| chr5:73086654 | G | T | 1 | a0002c0002t0002g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2246-935G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086654 | |||||||
| chr5:73086670 | A | T | 1 | a0001c0003t0003g0280 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2246-919A>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086670 | |||||||
| chr5:73086745 | G | T | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2246-844G>T | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086745 | |||||||
| chr5:73086751 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2246-838A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73086751 | |||||||
| chr5:73087167 | A | G | 2 | a0001c0003t0005g0233 a0001c0003t0005g0234 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2246-422A>G | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73087167 | |||||||
| chr5:73087362 | C | A | 2 | a0001c0003t0003g0276 a0001c0003t0003g0277 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2246-227C>A | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 24/25 | chr5 | 73087362 | |||||||
| chr5:73087775 | T | C | 1 | a0001c0001t0013g0192 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2410+22T>C | FCHO2 | ENSG00000157107.14 | transcript | ENST00000430046.7 | protein_coding | 25/25 | chr5 | 73087775 |