Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22862 |
| ensemblid | ENSG00000102531.16 |
| hgncid | 20296 |
| symbol | FNDC3A |
| name | fibronectin type III domain containing 3A |
| refseq_nuc | NM_001079673.2 |
| refseq_prot | NP_001073141.1 |
| ensembl_nuc | ENST00000492622.6 |
| ensembl_prot | ENSP00000417257.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 48975912 |
| end | 49209779 |
| strand | + |
| ver | v1.2 |
| region | chr13:48975912-49209779 |
| region5000 | chr13:48970912-49214779 |
| regionname0 | FNDC3A_chr13_48975912_49209779 |
| regionname5000 | FNDC3A_chr13_48970912_49214779 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1198 | 277 | 68 | 46 | 125 | 6 | 30 | 97 | FNDC3A_chr13_48970912_49214779 | FNDC3A | MAEHP others(1193): Show |
chr13 | 48970912 | 49214779 |
| a0002 | 0/0 | 1198 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | MAEHP others(1193): Show |
chr13 | 48970912 | 49214779 |
| a0003 | 0/0 | 1198 | 5 | 0 | 0 | 0 | 4 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | MAEHP others(1193): Show |
chr13 | 48970912 | 49214779 |
| a0004 | 0/0 | 1198 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | MAEHP others(1193): Show |
chr13 | 48970912 | 49214779 |
| a0005 | 0/0 | 1198 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | MAEHP others(1193): Show |
chr13 | 48970912 | 49214779 |
| a0006 | 0/0 | 1198 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | MAEHP others(1193): Show |
chr13 | 48970912 | 49214779 |
| a0007 | 0/0 | 1198 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | MAEHP others(1193): Show |
chr13 | 48970912 | 49214779 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3594 | 256 | 61 | 44 | 117 | 6 | 26 | FNDC3A_chr13_48970912_49214779 | FNDC3A | ATGGC others(3589): Show |
chr13 | 48970912 | 49214779 | ||
| a0001c0002 | 0/0 | 3594 | 18 | 5 | 1 | 8 | 0 | 4 | FNDC3A_chr13_48970912_49214779 | FNDC3A | ATGGC others(3589): Show |
chr13 | 48970912 | 49214779 | ||
| a0001c0005 | 0/0 | 3594 | 2 | 1 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | ATGGC others(3589): Show |
chr13 | 48970912 | 49214779 | ||
| a0001c0010 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | ATGGC others(3589): Show |
chr13 | 48970912 | 49214779 | ||
| a0002c0003 | 0/0 | 3594 | 6 | 6 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | ATGGC others(3589): Show |
chr13 | 48970912 | 49214779 | ||
| a0003c0004 | 0/0 | 3594 | 5 | 0 | 0 | 0 | 4 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | ATGGC others(3589): Show |
chr13 | 48970912 | 49214779 | ||
| a0004c0007 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | ATGGC others(3589): Show |
chr13 | 48970912 | 49214779 | ||
| a0005c0008 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | ATGGC others(3589): Show |
chr13 | 48970912 | 49214779 | ||
| a0006c0006 | 0/0 | 3594 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | ATGGC others(3589): Show |
chr13 | 48970912 | 49214779 | ||
| a0007c0009 | 0/0 | 3594 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | ATGGC others(3589): Show |
chr13 | 48970912 | 49214779 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6286 | 238 | 58 | 42 | 104 | 6 | 26 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0001c0001t0002 | 0/0 | 6286 | 10 | 0 | 1 | 9 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0001c0001t0003 | 0/0 | 6286 | 2 | 2 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0001c0001t0005 | 0/0 | 6286 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0001c0001t0006 | 0/0 | 6286 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0001c0001t0007 | 0/0 | 6286 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0001c0001t0008 | 0/0 | 6286 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0001c0001t0009 | 0/0 | 6274 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6269): Show |
chr13 | 48970912 | 49214779 |
| a0001c0001t0010 | 0/0 | 6286 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0001c0002t0001 | 0/0 | 6286 | 18 | 5 | 1 | 8 | 0 | 4 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0001c0005t0001 | 0/0 | 6286 | 2 | 1 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0001c0010t0004 | 0/0 | 6286 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0002c0003t0001 | 0/0 | 6286 | 6 | 6 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0003c0004t0001 | 0/0 | 6286 | 5 | 0 | 0 | 0 | 4 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0004c0007t0001 | 0/0 | 6286 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0005c0008t0001 | 0/0 | 6286 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0006c0006t0001 | 0/0 | 6286 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| a0007c0009t0001 | 0/0 | 6286 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | CTCCC others(6281): Show |
chr13 | 48970912 | 49214779 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0276 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0001t0010g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0005t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0001c0010t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0002c0003t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0002c0003t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0002c0003t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0002c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0002c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0002c0003t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0003c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0003c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0003c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0003c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0003c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0004c0007t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0005c0008t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0006c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| a0007c0009t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | FIN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00280 | hp2 | a0003 | c0004 | t0001 | g0035 | EUR | FIN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00733 | hp2 | a0001 | c0001 | t0010 | g0109 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG00741 | hp2 | a0001 | c0005 | t0001 | g0156 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | CLM | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01515 | hp1 | a0003 | c0004 | t0001 | g0042 | EUR | IBS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | IBS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | IBS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01516 | hp2 | a0003 | c0004 | t0001 | g0031 | EUR | IBS | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01891 | hp2 | a0001 | c0010 | t0004 | g0153 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0002 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0003 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0005 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03017 | hp1 | a0003 | c0004 | t0001 | g0045 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03130 | hp1 | a0004 | c0007 | t0001 | g0191 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03540 | hp1 | a0005 | c0008 | t0001 | g0123 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | STU | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0088 | SAS | BEB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0102 | SAS | BEB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | STU | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18906 | hp1 | a0001 | c0005 | t0001 | g0155 | AFR | YRI | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18978 | hp1 | a0001 | c0001 | t0007 | g0225 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18981 | hp1 | a0006 | c0006 | t0001 | g0074 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0204 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | LWK | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | LWK | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19054 | hp1 | a0001 | c0001 | t0009 | g0202 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0051 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | YRI | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | TSI | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA20805 | hp2 | a0003 | c0004 | t0001 | g0028 | EUR | TSI | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | GIH | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA20905 | hp2 | a0007 | c0009 | t0001 | g0194 | SAS | GIH | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | MSL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | USA | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | USA | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0276 | REF | REF | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0152 | REF | REF | FNDC3A_chr13_48970912_49214779 | FNDC3A | chr13 | 48970912 | 49214779 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49131203 | A | G | 1 | a0002 | 6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
missense_variant | MODERATE | c.319A>G | p.Ser107Gly | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/26 | 624/6286 | 319/3597 | 107/1198 | chr13 | 49131203 | |||
| chr13:49145784 | G | A | 1 | a0006 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.826G>A | p.Asp276Asn | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/26 | 1131/6286 | 826/3597 | 276/1198 | chr13 | 49145784 | |||
| chr13:49168693 | T | C | 1 | a0004 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1118T>C | p.Ile373Thr | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/26 | 1423/6286 | 1118/3597 | 373/1198 | chr13 | 49168693 | |||
| chr13:49191259 | A | G | 1 | a0007 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.2101A>G | p.Met701Val | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/26 | 2406/6286 | 2101/3597 | 701/1198 | chr13 | 49191259 | |||
| chr13:49198558 | G | C | 1 | a0005 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.2971G>C | p.Glu991Gln | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/26 | 3276/6286 | 2971/3597 | 991/1198 | chr13 | 49198558 | |||
| chr13:49201861 | A | G | 1 | a0003 | 5 | HG00280.hp2 HG01515.hp1 HG01516.hp2 others(2): Show |
missense_variant | MODERATE | c.3049A>G | p.Thr1017Ala | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/26 | 3354/6286 | 3049/3597 | 1017/1198 | chr13 | 49201861 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49145783 | C | T | 1 | a0001c0005 | 2 | HG00741.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.825C>T | p.Ser275Ser | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/26 | 1130/6286 | 825/3597 | 275/1198 | chr13 | 49145783 | |||
| chr13:49186098 | C | T | 1 | a0001c0010 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1752C>T | p.Thr584Thr | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 15/26 | 2057/6286 | 1752/3597 | 584/1198 | chr13 | 49186098 | |||
| chr13:49201944 | A | G | 1 | a0001c0002 | 18 | HG01496.hp2 HG02055.hp2 HG02132.hp2 others(15): Show |
synonymous_variant | LOW | c.3132A>G | p.Lys1044Lys | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/26 | 3437/6286 | 3132/3597 | 1044/1198 | chr13 | 49201944 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:48975923 | G | T | 1 | a0001c0001t0010 | 1 | HG00733.hp2 | 5_prime_UTR_variant | MODIFIER | c.-294G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/26 | 30268 | chr13 | 48975923 | ||||||
| chr13:48975992 | G | C | 1 | a0001c0001t0003 | 2 | HG02896.hp2 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-225G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/26 | 30199 | chr13 | 48975992 | ||||||
| chr13:48976033 | G | A | 1 | a0001c0010t0004 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-184G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/26 | 30158 | chr13 | 48976033 | ||||||
| chr13:48976052 | GCGCGCCG others(5): Show |
G | 1 | a0001c0001t0009 | 1 | NA19054.hp1 | 5_prime_UTR_variant | MODIFIER | c.-160_-149delCCGGCG others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/26 | 30123 | INFO_REALIGN_3_PRIME | chr13 | 48976052 | |||||
| chr13:48976135 | G | A | 1 | a0001c0001t0005 | 1 | NA18982.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/26 | 30056 | chr13 | 48976135 | ||||||
| chr13:49207547 | G | A | 1 | a0001c0001t0006 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*152G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 152 | chr13 | 49207547 | ||||||
| chr13:49209079 | A | T | 1 | a0001c0001t0002 | 10 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1684A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1684 | chr13 | 49209079 | ||||||
| chr13:49209126 | T | C | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1731T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1731 | chr13 | 49209126 | ||||||
| chr13:49209127 | G | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1732G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1732 | chr13 | 49209127 | ||||||
| chr13:49209129 | G | T | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1734G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1734 | chr13 | 49209129 | ||||||
| chr13:49209130 | A | G | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1735A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1735 | chr13 | 49209130 | ||||||
| chr13:49209137 | T | C | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1742T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1742 | chr13 | 49209137 | ||||||
| chr13:49209138 | C | T | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1743C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1743 | chr13 | 49209138 | ||||||
| chr13:49209139 | T | G | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1744T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1744 | chr13 | 49209139 | ||||||
| chr13:49209140 | A | G | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1745A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1745 | chr13 | 49209140 | ||||||
| chr13:49209144 | A | G | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1749A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1749 | chr13 | 49209144 | ||||||
| chr13:49209145 | C | G | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1750C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1750 | chr13 | 49209145 | ||||||
| chr13:49209148 | C | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1753C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1753 | chr13 | 49209148 | ||||||
| chr13:49209150 | T | C | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1755T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1755 | chr13 | 49209150 | ||||||
| chr13:49209151 | T | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1756T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1756 | chr13 | 49209151 | ||||||
| chr13:49209152 | A | C | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1757A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1757 | chr13 | 49209152 | ||||||
| chr13:49209153 | A | C | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1758A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1758 | chr13 | 49209153 | ||||||
| chr13:49209154 | A | C | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1759A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1759 | chr13 | 49209154 | ||||||
| chr13:49209155 | G | T | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1760G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1760 | chr13 | 49209155 | ||||||
| chr13:49209157 | G | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1762G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1762 | chr13 | 49209157 | ||||||
| chr13:49209158 | C | T | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1763C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1763 | chr13 | 49209158 | ||||||
| chr13:49209165 | T | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1770T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1770 | chr13 | 49209165 | ||||||
| chr13:49209170 | G | T | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1775G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1775 | chr13 | 49209170 | ||||||
| chr13:49209176 | A | T | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1781A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1781 | chr13 | 49209176 | ||||||
| chr13:49209178 | G | T | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1783G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1783 | chr13 | 49209178 | ||||||
| chr13:49209180 | G | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1785G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1785 | chr13 | 49209180 | ||||||
| chr13:49209181 | T | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1786T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1786 | chr13 | 49209181 | ||||||
| chr13:49209182 | C | T | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1787C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1787 | chr13 | 49209182 | ||||||
| chr13:49209183 | T | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1788T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1788 | chr13 | 49209183 | ||||||
| chr13:49209184 | G | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1789G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1789 | chr13 | 49209184 | ||||||
| chr13:49209186 | G | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1791 | chr13 | 49209186 | ||||||
| chr13:49209194 | G | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1799G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1799 | chr13 | 49209194 | ||||||
| chr13:49209199 | G | T | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1804G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1804 | chr13 | 49209199 | ||||||
| chr13:49209201 | G | C | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1806G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1806 | chr13 | 49209201 | ||||||
| chr13:49209203 | T | G | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1808T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1808 | chr13 | 49209203 | ||||||
| chr13:49209219 | T | G | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1824T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 1824 | chr13 | 49209219 | ||||||
| chr13:49209494 | A | G | 1 | a0001c0001t0008 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2099A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 26/26 | 2099 | chr13 | 49209494 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:48976209 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-40+32C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48976209 | |||||||
| chr13:48976319 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-40+142G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48976319 | |||||||
| chr13:48976510 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40+333G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48976510 | |||||||
| chr13:48977071 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-40+894G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48977071 | |||||||
| chr13:48977152 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-40+975A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48977152 | |||||||
| chr13:48977306 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-40+1129C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48977306 | |||||||
| chr13:48977352 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40+1175A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48977352 | |||||||
| chr13:48977614 | A | T | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-40+1437A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48977614 | |||||||
| chr13:48978135 | G | A | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-40+1958G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48978135 | |||||||
| chr13:48978136 | TGTGA | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-40+1962_-40+1965d others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48978136 | ||||||
| chr13:48978646 | G | GT | 5 | a0001c0001t0001g0122 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG01167.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40+2478dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48978646 | ||||||
| chr13:48978721 | A | G | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 |
3 | HG02723.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-40+2544A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48978721 | |||||||
| chr13:48978954 | A | G | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-40+2777A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48978954 | |||||||
| chr13:48979000 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-40+2823C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979000 | |||||||
| chr13:48979077 | T | C | 1 | a0005c0008t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-40+2900T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979077 | |||||||
| chr13:48979172 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-40+2995A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979172 | |||||||
| chr13:48979178 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40+3001C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979178 | |||||||
| chr13:48979180 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-40+3003T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979180 | |||||||
| chr13:48979251 | G | A | 1 | a0002c0003t0001g0002 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-40+3074G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979251 | |||||||
| chr13:48979291 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-40+3114C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979291 | |||||||
| chr13:48979537 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-40+3360A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979537 | |||||||
| chr13:48979778 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-40+3601G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979778 | |||||||
| chr13:48979841 | C | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-40+3664C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979841 | |||||||
| chr13:48979992 | T | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(270): Show |
273 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.-40+3815T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48979992 | |||||||
| chr13:48980058 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18943.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-40+3881T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48980058 | |||||||
| chr13:48980094 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-40+3917G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48980094 | |||||||
| chr13:48980344 | G | T | 13 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(10): Show |
13 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40+4167G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48980344 | |||||||
| chr13:48980533 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-40+4356A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48980533 | |||||||
| chr13:48980550 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-40+4373C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48980550 | |||||||
| chr13:48980569 | A | G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG00438.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-40+4392A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48980569 | |||||||
| chr13:48981048 | C | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-40+4871C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48981048 | |||||||
| chr13:48981089 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-40+4912G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48981089 | |||||||
| chr13:48981343 | A | C | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG02132.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-40+5166A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48981343 | |||||||
| chr13:48981820 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-40+5643A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48981820 | |||||||
| chr13:48981831 | TG | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.-40+5659delG | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48981831 | ||||||
| chr13:48981919 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-40+5742C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48981919 | |||||||
| chr13:48981977 | G | A | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40+5800G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48981977 | |||||||
| chr13:48982097 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | NA18612.hp2 NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-40+5920T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48982097 | |||||||
| chr13:48982445 | T | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40+6268T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48982445 | |||||||
| chr13:48982678 | C | A | 1 | a0001c0002t0001g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-40+6501C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48982678 | |||||||
| chr13:48983319 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-40+7142A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48983319 | |||||||
| chr13:48983587 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-40+7410G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48983587 | |||||||
| chr13:48983669 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-40+7492A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48983669 | |||||||
| chr13:48983724 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-40+7547T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48983724 | |||||||
| chr13:48983774 | T | C | 10 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0171 others(7): Show |
10 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40+7597T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48983774 | |||||||
| chr13:48983846 | A | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG03688.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-40+7669A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48983846 | |||||||
| chr13:48983887 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01074.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+7710C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48983887 | |||||||
| chr13:48983977 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(150): Show |
153 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-40+7800G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48983977 | |||||||
| chr13:48983980 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-40+7803A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48983980 | |||||||
| chr13:48984124 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-40+7947T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48984124 | |||||||
| chr13:48984874 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-40+8697G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48984874 | |||||||
| chr13:48984903 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-40+8726C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48984903 | |||||||
| chr13:48984984 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-40+8807G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48984984 | |||||||
| chr13:48985339 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-40+9162G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48985339 | |||||||
| chr13:48985612 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-40+9435G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48985612 | |||||||
| chr13:48985654 | A | T | 13 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(10): Show |
13 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40+9477A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48985654 | |||||||
| chr13:48985812 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01074.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+9635G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48985812 | |||||||
| chr13:48985877 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-40+9700T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48985877 | |||||||
| chr13:48986138 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40+9961A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986138 | |||||||
| chr13:48986179 | A | G | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.-40+10002A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986179 | |||||||
| chr13:48986210 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40+10033G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986210 | |||||||
| chr13:48986265 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-40+10088G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986265 | |||||||
| chr13:48986305 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-40+10128A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986305 | |||||||
| chr13:48986333 | CAA | C | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-40+10157_-40+1015 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986333 | |||||||
| chr13:48986378 | G | A | 66 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(63): Show |
66 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.-40+10201G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986378 | |||||||
| chr13:48986385 | G | GT | 80 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0160 others(77): Show |
80 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-40+10236dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48986385 | ||||||
| chr13:48986385 | G | GTT | 58 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0075 others(55): Show |
58 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-40+10235_-40+1023 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48986385 | ||||||
| chr13:48986385 | G | GTTT | 70 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(67): Show |
70 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-40+10234_-40+1023 others(7): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48986385 | ||||||
| chr13:48986385 | G | GTTTT | 38 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0052 others(35): Show |
38 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-40+10233_-40+1023 others(8): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48986385 | ||||||
| chr13:48986385 | G | GTTTTT | 15 | a0001c0001t0001g0011 a0001c0001t0001g0068 a0001c0001t0001g0069 others(12): Show |
15 | HG00544.hp1 HG01243.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-40+10232_-40+1023 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48986385 | ||||||
| chr13:48986385 | GTTT | G | 10 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(7): Show |
10 | HG01074.hp2 HG02257.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40+10234_-40+1023 others(7): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48986385 | ||||||
| chr13:48986385 | GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | NA18956.hp1 NA18968.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-40+10227_-40+1023 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48986385 | ||||||
| chr13:48986398 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-40+10221T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986398 | |||||||
| chr13:48986474 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-40+10297C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986474 | |||||||
| chr13:48986482 | G | A | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-40+10305G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986482 | |||||||
| chr13:48986697 | G | A | 99 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(96): Show |
99 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-40+10520G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986697 | |||||||
| chr13:48986837 | A | C | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-40+10660A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986837 | |||||||
| chr13:48986918 | CAT | C | 8 | a0001c0001t0001g0075 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG00639.hp1 HG00733.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40+10742_-40+1074 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48986918 | |||||||
| chr13:48987025 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-40+10848A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48987025 | |||||||
| chr13:48987153 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-40+10976A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48987153 | |||||||
| chr13:48987277 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.-40+11100G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48987277 | |||||||
| chr13:48987351 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18943.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-40+11174T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48987351 | |||||||
| chr13:48987360 | T | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(7): Show |
10 | HG01167.hp2 HG01175.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40+11183T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48987360 | |||||||
| chr13:48987437 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.-40+11260T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48987437 | |||||||
| chr13:48987626 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-40+11449C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48987626 | |||||||
| chr13:48987798 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-40+11621A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48987798 | |||||||
| chr13:48987947 | C | T | 1 | a0001c0002t0001g0117 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-40+11770C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48987947 | |||||||
| chr13:48988231 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-40+12054T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48988231 | |||||||
| chr13:48988515 | T | C | 1 | a0001c0001t0001g0023 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-40+12338T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48988515 | |||||||
| chr13:48988844 | C | CA | 9 | a0001c0001t0001g0024 a0001c0001t0001g0125 a0001c0001t0001g0137 others(6): Show |
9 | HG00544.hp2 HG01074.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-40+12682dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48988844 | ||||||
| chr13:48988844 | CA | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0128 others(9): Show |
12 | HG01074.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40+12682delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48988844 | ||||||
| chr13:48989174 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-40+12997C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48989174 | |||||||
| chr13:48989208 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-40+13031C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48989208 | |||||||
| chr13:48989284 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-40+13107A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48989284 | |||||||
| chr13:48989564 | G | A | 99 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(96): Show |
99 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-40+13387G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48989564 | |||||||
| chr13:48989697 | A | G | 16 | a0001c0001t0001g0168 a0001c0001t0001g0245 a0001c0001t0001g0247 others(13): Show |
16 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-40+13520A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48989697 | |||||||
| chr13:48989704 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-40+13527A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48989704 | |||||||
| chr13:48989754 | CT | C | 31 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0075 others(28): Show |
31 | HG00639.hp1 HG00733.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-40+13593delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48989754 | ||||||
| chr13:48989869 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-40+13692A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48989869 | |||||||
| chr13:48989915 | C | G | 1 | a0002c0003t0001g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-40+13738C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48989915 | |||||||
| chr13:48989986 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-40+13809G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48989986 | |||||||
| chr13:48990215 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0246 |
2 | NA18954.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-40+14038C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48990215 | |||||||
| chr13:48990219 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-40+14042A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48990219 | |||||||
| chr13:48990219 | A | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0246 |
2 | NA18954.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-40+14042A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48990219 | |||||||
| chr13:48990423 | A | C | 1 | a0006c0006t0001g0074 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-40+14246A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48990423 | |||||||
| chr13:48990588 | C | CA | 55 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0048 others(52): Show |
55 | HG00639.hp2 HG01070.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.-40+14435dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48990588 | ||||||
| chr13:48990588 | C | CAA | 189 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(186): Show |
189 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.-40+14434_-40+1443 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48990588 | ||||||
| chr13:48990588 | C | CAAA | 21 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0110 others(18): Show |
21 | HG00597.hp2 HG01106.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.-40+14433_-40+1443 others(7): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48990588 | ||||||
| chr13:48990588 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0096 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-40+14426_-40+1443 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48990588 | ||||||
| chr13:48990677 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-40+14500G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48990677 | |||||||
| chr13:48990914 | CAT | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40+14738_-40+1473 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48990914 | |||||||
| chr13:48990945 | C | T | 4 | a0001c0002t0001g0085 a0001c0002t0001g0119 a0001c0002t0001g0120 others(1): Show |
4 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+14768C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48990945 | |||||||
| chr13:48991093 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-40+14916T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48991093 | |||||||
| chr13:48991128 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-40+14951C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48991128 | |||||||
| chr13:48991191 | T | A | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-39-14961T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48991191 | |||||||
| chr13:48991325 | T | G | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-39-14827T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48991325 | |||||||
| chr13:48991992 | A | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-39-14160A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48991992 | |||||||
| chr13:48992133 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-39-14019A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48992133 | |||||||
| chr13:48992151 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-39-14001A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48992151 | |||||||
| chr13:48992379 | T | A | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-39-13773T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48992379 | |||||||
| chr13:48992469 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-13683A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48992469 | |||||||
| chr13:48992542 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-39-13610C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48992542 | |||||||
| chr13:48992706 | T | C | 1 | a0005c0008t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-39-13446T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48992706 | |||||||
| chr13:48993772 | C | G | 2 | a0001c0001t0001g0124 a0005c0008t0001g0123 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-39-12380C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48993772 | |||||||
| chr13:48993808 | T | G | 8 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
8 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-12344T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48993808 | |||||||
| chr13:48993971 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-39-12181A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48993971 | |||||||
| chr13:48994182 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-39-11970A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48994182 | |||||||
| chr13:48994243 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-39-11909G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48994243 | |||||||
| chr13:48994710 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-39-11442G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48994710 | |||||||
| chr13:48994743 | C | T | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39-11409C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48994743 | |||||||
| chr13:48994782 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-39-11370A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48994782 | |||||||
| chr13:48994851 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-39-11301G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48994851 | |||||||
| chr13:48994933 | T | G | 14 | a0001c0001t0001g0115 a0001c0002t0001g0009 a0001c0002t0001g0086 others(11): Show |
14 | HG01496.hp2 HG02055.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-11219T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48994933 | |||||||
| chr13:48995310 | CT | C | 7 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
7 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39-10830delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48995310 | ||||||
| chr13:48995507 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-39-10645T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48995507 | |||||||
| chr13:48995556 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-39-10596C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48995556 | |||||||
| chr13:48995711 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-39-10441G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48995711 | |||||||
| chr13:48995789 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-39-10363A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48995789 | |||||||
| chr13:48995875 | C | T | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-10277C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48995875 | |||||||
| chr13:48995955 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-39-10197C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48995955 | |||||||
| chr13:48996008 | T | C | 1 | a0001c0001t0001g0026 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-39-10144T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48996008 | |||||||
| chr13:48996180 | A | G | 12 | a0001c0001t0001g0185 a0001c0001t0001g0190 a0001c0001t0001g0217 others(9): Show |
12 | HG01433.hp2 HG01928.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-9972A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48996180 | |||||||
| chr13:48996494 | T | A | 99 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(96): Show |
99 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-39-9658T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48996494 | |||||||
| chr13:48996499 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0192 a0004c0007t0001g0191 |
3 | HG02965.hp1 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-39-9653G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48996499 | |||||||
| chr13:48997018 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-39-9134G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48997018 | |||||||
| chr13:48997051 | G | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.-39-9101G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48997051 | |||||||
| chr13:48997058 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-39-9094C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48997058 | |||||||
| chr13:48997066 | GA | G | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG02698.hp1 HG03209.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-9071delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 48997066 | ||||||
| chr13:48997219 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-39-8933C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48997219 | |||||||
| chr13:48997286 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-39-8866A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48997286 | |||||||
| chr13:48997750 | T | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-39-8402T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48997750 | |||||||
| chr13:48998009 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-39-8143G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48998009 | |||||||
| chr13:48998056 | T | C | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-39-8096T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48998056 | |||||||
| chr13:48998346 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-39-7806G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48998346 | |||||||
| chr13:48998818 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-39-7334A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48998818 | |||||||
| chr13:48999087 | G | A | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-39-7065G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48999087 | |||||||
| chr13:48999123 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-39-7029C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48999123 | |||||||
| chr13:48999148 | G | A | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-39-7004G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48999148 | |||||||
| chr13:48999279 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-39-6873G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48999279 | |||||||
| chr13:48999412 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-39-6740A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48999412 | |||||||
| chr13:48999457 | G | C | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-39-6695G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48999457 | |||||||
| chr13:48999763 | G | A | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-39-6389G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48999763 | |||||||
| chr13:48999956 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.-39-6196G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 48999956 | |||||||
| chr13:49000027 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0146 |
2 | NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-39-6125A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49000027 | |||||||
| chr13:49000065 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-39-6087T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49000065 | |||||||
| chr13:49000230 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-39-5922C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49000230 | |||||||
| chr13:49000271 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-39-5881T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49000271 | |||||||
| chr13:49000486 | G | C | 1 | a0001c0001t0001g0233 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-39-5666G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49000486 | |||||||
| chr13:49000495 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-39-5657T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49000495 | |||||||
| chr13:49000702 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-5450T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49000702 | |||||||
| chr13:49000940 | T | C | 15 | a0001c0001t0001g0162 a0001c0001t0001g0185 a0001c0001t0001g0190 others(12): Show |
15 | HG01106.hp2 HG01433.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.-39-5212T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49000940 | |||||||
| chr13:49000964 | T | TTG | 115 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(112): Show |
115 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-39-5168_-39-5167d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 49000964 | ||||||
| chr13:49000964 | T | TTGTG | 8 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-5170_-39-5167d others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 49000964 | ||||||
| chr13:49001022 | C | CTG | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
13 | HG01167.hp2 HG01175.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-39-5127_-39-5126d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 49001022 | ||||||
| chr13:49001323 | C | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-4829C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49001323 | |||||||
| chr13:49001371 | T | C | 99 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(96): Show |
99 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-39-4781T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49001371 | |||||||
| chr13:49001464 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-39-4688G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49001464 | |||||||
| chr13:49001649 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-4503C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49001649 | |||||||
| chr13:49001701 | C | T | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 |
3 | HG02723.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-39-4451C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49001701 | |||||||
| chr13:49001747 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-39-4405G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49001747 | |||||||
| chr13:49001801 | G | T | 1 | a0002c0003t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-39-4351G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49001801 | |||||||
| chr13:49001829 | T | C | 1 | a0001c0001t0001g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-39-4323T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49001829 | |||||||
| chr13:49002088 | A | G | 1 | a0001c0001t0001g0243 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-39-4064A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49002088 | |||||||
| chr13:49002114 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-39-4038C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49002114 | |||||||
| chr13:49002338 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-39-3814A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49002338 | |||||||
| chr13:49002454 | G | A | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-39-3698G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49002454 | |||||||
| chr13:49002498 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-39-3654G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49002498 | |||||||
| chr13:49002619 | G | A | 7 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0001g0197 others(4): Show |
7 | HG02257.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39-3533G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49002619 | |||||||
| chr13:49002885 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-39-3267G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49002885 | |||||||
| chr13:49003029 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-39-3123T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49003029 | |||||||
| chr13:49003191 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-39-2961A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49003191 | |||||||
| chr13:49003220 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-39-2932C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49003220 | |||||||
| chr13:49003360 | C | T | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 |
3 | HG02723.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-39-2792C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49003360 | |||||||
| chr13:49003460 | AT | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-39-2691delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49003460 | |||||||
| chr13:49003645 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-39-2507C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49003645 | |||||||
| chr13:49003703 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-39-2449C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49003703 | |||||||
| chr13:49003859 | G | C | 1 | a0001c0005t0001g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-39-2293G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49003859 | |||||||
| chr13:49003899 | A | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0242 |
3 | HG02630.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-39-2253A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49003899 | |||||||
| chr13:49004098 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-39-2054A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49004098 | |||||||
| chr13:49004127 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-39-2025G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49004127 | |||||||
| chr13:49004176 | A | T | 4 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0223 others(1): Show |
4 | NA18959.hp1 NA18969.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-1976A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49004176 | |||||||
| chr13:49004211 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-39-1941A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49004211 | |||||||
| chr13:49004383 | A | G | 1 | a0002c0003t0001g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-39-1769A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49004383 | |||||||
| chr13:49004463 | A | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-1689A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49004463 | |||||||
| chr13:49004493 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-39-1659G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49004493 | |||||||
| chr13:49004673 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-39-1479C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49004673 | |||||||
| chr13:49005073 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-39-1079C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49005073 | |||||||
| chr13:49005334 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-39-818T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49005334 | |||||||
| chr13:49005473 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-39-679T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49005473 | |||||||
| chr13:49005498 | GT | G | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-39-647delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr13 | 49005498 | ||||||
| chr13:49005918 | A | C | 1 | a0001c0001t0001g0213 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-39-234A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49005918 | |||||||
| chr13:49006022 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-39-130A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 1/25 | chr13 | 49006022 | |||||||
| chr13:49006327 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.99+38A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49006327 | |||||||
| chr13:49006415 | C | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+126C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49006415 | |||||||
| chr13:49007024 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00621.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.99+735T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49007024 | |||||||
| chr13:49007250 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.99+961A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49007250 | |||||||
| chr13:49007382 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.99+1093A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49007382 | |||||||
| chr13:49007550 | A | T | 1 | a0001c0001t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.99+1261A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49007550 | |||||||
| chr13:49007571 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.99+1282G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49007571 | |||||||
| chr13:49007618 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.99+1329C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49007618 | |||||||
| chr13:49008361 | C | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.99+2072C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49008361 | |||||||
| chr13:49008400 | T | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01074.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+2111T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49008400 | |||||||
| chr13:49008463 | T | TGTC | 273 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(270): Show |
273 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.99+2176_99+2177ins others(3): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49008463 | ||||||
| chr13:49008604 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+2315A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49008604 | |||||||
| chr13:49008937 | T | TTATTAAC others(1): Show |
152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(149): Show |
152 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.99+2653_99+2654ins others(8): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49008937 | ||||||
| chr13:49009000 | G | A | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG02132.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.99+2711G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49009000 | |||||||
| chr13:49009054 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.99+2765G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49009054 | |||||||
| chr13:49009114 | G | A | 11 | a0001c0001t0001g0184 a0001c0001t0001g0198 a0001c0001t0001g0199 others(8): Show |
11 | HG00597.hp1 HG02523.hp2 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+2825G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49009114 | |||||||
| chr13:49009222 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+2933A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49009222 | |||||||
| chr13:49009502 | C | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+3213C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49009502 | |||||||
| chr13:49009710 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(149): Show |
152 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.99+3421G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49009710 | |||||||
| chr13:49009722 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+3433C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49009722 | |||||||
| chr13:49009999 | A | G | 118 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(115): Show |
118 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.99+3710A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49009999 | |||||||
| chr13:49010404 | A | C | 4 | a0001c0001t0001g0212 a0001c0001t0001g0233 a0001c0001t0001g0241 others(1): Show |
4 | HG02074.hp1 HG02132.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+4115A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49010404 | |||||||
| chr13:49010420 | A | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(7): Show |
10 | HG01167.hp2 HG01175.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+4131A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49010420 | |||||||
| chr13:49010530 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.99+4241C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49010530 | |||||||
| chr13:49010627 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.99+4338C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49010627 | |||||||
| chr13:49010725 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.99+4436T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49010725 | |||||||
| chr13:49010826 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+4537A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49010826 | |||||||
| chr13:49010830 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+4541A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49010830 | |||||||
| chr13:49010832 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.99+4543A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49010832 | |||||||
| chr13:49011200 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+4911C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49011200 | |||||||
| chr13:49011240 | CT | C | 117 | a0001c0001t0001g0049 a0001c0001t0001g0140 a0001c0001t0001g0162 others(114): Show |
117 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.99+4962delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49011240 | ||||||
| chr13:49011242 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.99+4953T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49011242 | |||||||
| chr13:49011265 | G | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.99+4976G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49011265 | |||||||
| chr13:49011284 | A | C | 4 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0223 others(1): Show |
4 | NA18959.hp1 NA18969.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+4995A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49011284 | |||||||
| chr13:49011301 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.99+5012T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49011301 | |||||||
| chr13:49011326 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+5037C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49011326 | |||||||
| chr13:49011344 | C | T | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
13 | HG01167.hp2 HG01175.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+5055C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49011344 | |||||||
| chr13:49011444 | A | T | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.99+5155A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49011444 | |||||||
| chr13:49011524 | G | A | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99+5235G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49011524 | |||||||
| chr13:49011882 | T | C | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.99+5593T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49011882 | |||||||
| chr13:49012524 | A | G | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+6235A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49012524 | |||||||
| chr13:49012534 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.99+6245G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49012534 | |||||||
| chr13:49012542 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.99+6253T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49012542 | |||||||
| chr13:49012603 | C | T | 2 | a0001c0001t0001g0124 a0005c0008t0001g0123 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.99+6314C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49012603 | |||||||
| chr13:49012630 | A | G | 4 | a0001c0002t0001g0085 a0001c0002t0001g0119 a0001c0002t0001g0120 others(1): Show |
4 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+6341A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49012630 | |||||||
| chr13:49012697 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+6408G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49012697 | |||||||
| chr13:49012805 | A | ATG | 3 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0006 |
3 | HG02717.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.99+6550_99+6551dup others(2): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTG | 16 | a0001c0001t0001g0212 a0001c0001t0001g0233 a0001c0001t0001g0244 others(13): Show |
16 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+6548_99+6551dup others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTG | 10 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0226 others(7): Show |
10 | HG01074.hp1 HG01169.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+6546_99+6551dup others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTGT others(1): Show |
65 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0101 others(62): Show |
65 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.99+6544_99+6551dup others(8): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTGT others(3): Show |
61 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(58): Show |
61 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.99+6542_99+6551dup others(10): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTGT others(5): Show |
33 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0046 others(30): Show |
33 | HG00408.hp1 HG00621.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.99+6540_99+6551dup others(12): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTGT others(7): Show |
52 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(49): Show |
52 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.99+6538_99+6551dup others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTGT others(9): Show |
23 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0039 others(20): Show |
23 | HG00438.hp2 HG00597.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+6536_99+6551dup others(16): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTGT others(11): Show |
12 | a0001c0001t0001g0065 a0001c0001t0001g0072 a0001c0001t0001g0133 others(9): Show |
12 | HG01975.hp2 HG02074.hp2 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+6534_99+6551dup others(18): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTGT others(13): Show |
3 | a0001c0002t0001g0113 a0001c0002t0001g0119 a0001c0002t0001g0121 |
3 | HG02723.hp2 NA19060.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.99+6532_99+6551dup others(20): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTGT others(15): Show |
1 | a0001c0001t0001g0096 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+6530_99+6551dup others(22): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTGT others(17): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.99+6528_99+6551dup others(24): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | ATGTGTGT others(19): Show |
1 | a0003c0004t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.99+6526_99+6551dup others(26): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49012805 | ||||||
| chr13:49012805 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.99+6516A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49012805 | |||||||
| chr13:49012917 | A | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | NA18956.hp1 NA18968.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.99+6628A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49012917 | |||||||
| chr13:49013053 | C | T | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.99+6764C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013053 | |||||||
| chr13:49013117 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+6828A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013117 | |||||||
| chr13:49013361 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+7072T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013361 | |||||||
| chr13:49013369 | A | G | 5 | a0001c0001t0001g0186 a0001c0001t0001g0197 a0001c0001t0001g0224 others(2): Show |
5 | HG02257.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+7080A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013369 | |||||||
| chr13:49013436 | T | TTACATAT others(19): Show |
2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.99+7158_99+7183dup others(26): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49013436 | ||||||
| chr13:49013443 | T | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+7154T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013443 | |||||||
| chr13:49013453 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.99+7164T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013453 | |||||||
| chr13:49013487 | T | G | 1 | a0002c0003t0001g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+7198T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013487 | |||||||
| chr13:49013535 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+7246T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013535 | |||||||
| chr13:49013542 | A | G | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(13): Show |
16 | HG00280.hp2 HG00609.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+7253A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013542 | |||||||
| chr13:49013587 | C | G | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99+7298C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013587 | |||||||
| chr13:49013622 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.99+7333G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013622 | |||||||
| chr13:49013630 | ATGTATAC others(9): Show |
A | 1 | a0001c0001t0001g0198 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.99+7354_99+7369del others(16): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49013630 | ||||||
| chr13:49013646 | GTGTATAC others(1): Show |
G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
13 | HG01167.hp2 HG01175.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+7370_99+7377del others(8): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49013646 | ||||||
| chr13:49013660 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+7371A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013660 | |||||||
| chr13:49013687 | G | A | 13 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(10): Show |
13 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+7398G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013687 | |||||||
| chr13:49013882 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+7593A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49013882 | |||||||
| chr13:49014107 | A | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(15): Show |
18 | HG01074.hp2 HG01257.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+7818A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014107 | |||||||
| chr13:49014283 | T | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+7994T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014283 | |||||||
| chr13:49014304 | A | T | 14 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0077 others(11): Show |
14 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+8015A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014304 | |||||||
| chr13:49014395 | T | C | 1 | a0007c0009t0001g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.99+8106T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014395 | |||||||
| chr13:49014399 | T | C | 1 | a0001c0002t0001g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99+8110T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014399 | |||||||
| chr13:49014416 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+8127A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014416 | |||||||
| chr13:49014425 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+8136A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014425 | |||||||
| chr13:49014522 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.99+8233T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014522 | |||||||
| chr13:49014523 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.99+8234G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014523 | |||||||
| chr13:49014556 | C | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+8267C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014556 | |||||||
| chr13:49014728 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+8439T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014728 | |||||||
| chr13:49014739 | G | A | 118 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(115): Show |
118 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.99+8450G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014739 | |||||||
| chr13:49014863 | C | A | 124 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(121): Show |
124 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.99+8574C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014863 | |||||||
| chr13:49014870 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.99+8581G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49014870 | |||||||
| chr13:49015031 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+8742G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015031 | |||||||
| chr13:49015136 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.99+8847A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015136 | |||||||
| chr13:49015207 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.99+8918G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015207 | |||||||
| chr13:49015224 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+8935C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015224 | |||||||
| chr13:49015229 | T | G | 1 | a0001c0001t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.99+8940T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015229 | |||||||
| chr13:49015296 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+9007C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015296 | |||||||
| chr13:49015520 | C | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0009g0202 |
3 | HG00438.hp1 NA19054.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.99+9231C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015520 | |||||||
| chr13:49015520 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+9231C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015520 | |||||||
| chr13:49015521 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0009g0202 |
3 | HG00438.hp1 NA19054.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.99+9232G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015521 | |||||||
| chr13:49015547 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+9258G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015547 | |||||||
| chr13:49015917 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.99+9628G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015917 | |||||||
| chr13:49015956 | C | T | 1 | a0001c0001t0009g0202 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.99+9667C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015956 | |||||||
| chr13:49015998 | G | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+9709G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015998 | |||||||
| chr13:49015999 | G | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+9710G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49015999 | |||||||
| chr13:49016042 | A | G | 5 | a0001c0001t0001g0186 a0001c0001t0001g0197 a0001c0001t0001g0224 others(2): Show |
5 | HG02257.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+9753A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016042 | |||||||
| chr13:49016115 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.99+9826C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016115 | |||||||
| chr13:49016150 | G | A | 1 | a0005c0008t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.99+9861G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016150 | |||||||
| chr13:49016212 | A | G | 1 | a0002c0003t0001g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+9923A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016212 | |||||||
| chr13:49016282 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.99+9993C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016282 | |||||||
| chr13:49016364 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99+10075C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016364 | |||||||
| chr13:49016389 | G | A | 1 | a0001c0001t0010g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.99+10100G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016389 | |||||||
| chr13:49016448 | T | G | 1 | a0001c0001t0001g0024 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.99+10159T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016448 | |||||||
| chr13:49016449 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+10160C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016449 | |||||||
| chr13:49016459 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+10170A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016459 | |||||||
| chr13:49016580 | G | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0018 |
2 | NA18968.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.99+10291G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016580 | |||||||
| chr13:49016645 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.99+10356T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016645 | |||||||
| chr13:49016654 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(267): Show |
270 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.99+10365T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016654 | |||||||
| chr13:49016782 | A | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.99+10493A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016782 | |||||||
| chr13:49016786 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+10497A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016786 | |||||||
| chr13:49016851 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+10562C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016851 | |||||||
| chr13:49016856 | T | C | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+10567T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016856 | |||||||
| chr13:49016904 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+10615G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016904 | |||||||
| chr13:49016907 | C | T | 10 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0171 others(7): Show |
10 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+10618C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49016907 | |||||||
| chr13:49017035 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.99+10746T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017035 | |||||||
| chr13:49017155 | C | A | 1 | a0002c0003t0001g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+10866C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017155 | |||||||
| chr13:49017159 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.99+10870C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017159 | |||||||
| chr13:49017398 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.99+11109G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017398 | |||||||
| chr13:49017531 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.99+11242C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017531 | |||||||
| chr13:49017738 | C | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.99+11449C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017738 | |||||||
| chr13:49017798 | T | G | 8 | a0001c0001t0001g0168 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
8 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+11509T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017798 | |||||||
| chr13:49017940 | T | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(15): Show |
18 | HG01074.hp2 HG01257.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+11651T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017940 | |||||||
| chr13:49017962 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.99+11673G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017962 | |||||||
| chr13:49017970 | C | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+11681C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017970 | |||||||
| chr13:49017975 | G | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+11686G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49017975 | |||||||
| chr13:49018017 | C | G | 1 | a0001c0001t0001g0233 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.99+11728C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49018017 | |||||||
| chr13:49018080 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.99+11791T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49018080 | |||||||
| chr13:49018150 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.99+11861T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49018150 | |||||||
| chr13:49018273 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG02135.hp1 NA18956.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+11984G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49018273 | |||||||
| chr13:49018435 | G | C | 6 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+12146G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49018435 | |||||||
| chr13:49018477 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.99+12188A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49018477 | |||||||
| chr13:49018653 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.99+12364A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49018653 | |||||||
| chr13:49018879 | C | T | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG01891.hp1 HG02698.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+12590C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49018879 | |||||||
| chr13:49018976 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+12687C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49018976 | |||||||
| chr13:49018988 | A | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(25): Show |
28 | HG00408.hp1 HG00544.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+12699A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49018988 | |||||||
| chr13:49019048 | T | A | 28 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(25): Show |
28 | HG00408.hp1 HG00544.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+12759T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019048 | |||||||
| chr13:49019093 | C | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0002t0001g0119 others(2): Show |
5 | HG02723.hp2 HG02886.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+12804C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019093 | |||||||
| chr13:49019093 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.99+12804C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019093 | |||||||
| chr13:49019108 | C | T | 13 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(10): Show |
13 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+12819C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019108 | |||||||
| chr13:49019110 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.99+12821G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019110 | |||||||
| chr13:49019182 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.99+12893C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019182 | |||||||
| chr13:49019203 | C | T | 1 | a0001c0001t0007g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.99+12914C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019203 | |||||||
| chr13:49019248 | A | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+12959A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019248 | |||||||
| chr13:49019250 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+12961C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019250 | |||||||
| chr13:49019283 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+12994G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019283 | |||||||
| chr13:49019286 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+12997G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019286 | |||||||
| chr13:49019308 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.99+13019G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019308 | |||||||
| chr13:49019376 | C | G | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99+13087C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019376 | |||||||
| chr13:49019397 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.99+13108A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019397 | |||||||
| chr13:49019444 | C | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.99+13155C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019444 | |||||||
| chr13:49019462 | C | T | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99+13173C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019462 | |||||||
| chr13:49019532 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+13243C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019532 | |||||||
| chr13:49019540 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.99+13251G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019540 | |||||||
| chr13:49019607 | T | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+13318T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019607 | |||||||
| chr13:49019630 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.99+13341A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019630 | |||||||
| chr13:49019644 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.99+13355A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019644 | |||||||
| chr13:49019809 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.99+13520T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019809 | |||||||
| chr13:49019929 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+13640G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49019929 | |||||||
| chr13:49020045 | G | A | 4 | a0003c0004t0001g0028 a0003c0004t0001g0031 a0003c0004t0001g0035 others(1): Show |
4 | HG00280.hp2 HG01515.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+13756G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49020045 | |||||||
| chr13:49020056 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.99+13767A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49020056 | |||||||
| chr13:49020140 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.99+13851G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49020140 | |||||||
| chr13:49020179 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.99+13890G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49020179 | |||||||
| chr13:49020281 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0018 |
2 | NA18968.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.99+13992C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49020281 | |||||||
| chr13:49020386 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.99+14097G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49020386 | |||||||
| chr13:49020682 | G | A | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.99+14393G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49020682 | |||||||
| chr13:49020719 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+14430C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49020719 | |||||||
| chr13:49021053 | C | T | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.99+14764C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021053 | |||||||
| chr13:49021091 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.99+14802A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021091 | |||||||
| chr13:49021114 | A | G | 5 | a0001c0001t0001g0212 a0001c0001t0001g0233 a0001c0001t0001g0237 others(2): Show |
5 | HG02074.hp1 HG02132.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+14825A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021114 | |||||||
| chr13:49021195 | A | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.99+14906A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021195 | |||||||
| chr13:49021217 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.99+14928A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021217 | |||||||
| chr13:49021260 | G | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+14971G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021260 | |||||||
| chr13:49021560 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99+15271C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021560 | |||||||
| chr13:49021716 | C | T | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.99+15427C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021716 | |||||||
| chr13:49021751 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.99+15462C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021751 | |||||||
| chr13:49021753 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0209 |
2 | NA18998.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.99+15464A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021753 | |||||||
| chr13:49021827 | G | T | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.99+15538G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021827 | |||||||
| chr13:49021986 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0190 |
2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.99+15697G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49021986 | |||||||
| chr13:49022065 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+15776A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49022065 | |||||||
| chr13:49022523 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.99+16234A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49022523 | |||||||
| chr13:49022692 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.99+16403A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49022692 | |||||||
| chr13:49022789 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.99+16500A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49022789 | |||||||
| chr13:49022833 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.99+16544G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49022833 | |||||||
| chr13:49022878 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.99+16589A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49022878 | |||||||
| chr13:49022900 | A | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+16611A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49022900 | |||||||
| chr13:49023032 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.99+16743A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49023032 | |||||||
| chr13:49023145 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.99+16856G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49023145 | |||||||
| chr13:49023274 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.99+16985C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49023274 | |||||||
| chr13:49023275 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.99+16986A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49023275 | |||||||
| chr13:49023528 | C | T | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.99+17239C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49023528 | |||||||
| chr13:49023556 | C | A | 2 | a0001c0001t0001g0160 a0001c0001t0006g0161 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.99+17267C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49023556 | |||||||
| chr13:49023572 | T | A | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG01891.hp1 HG02698.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+17283T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49023572 | |||||||
| chr13:49024053 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.99+17764G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49024053 | |||||||
| chr13:49024398 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.99+18109C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49024398 | |||||||
| chr13:49024578 | C | T | 118 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(115): Show |
118 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.99+18289C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49024578 | |||||||
| chr13:49024691 | T | A | 16 | a0001c0001t0001g0058 a0001c0001t0001g0135 a0001c0001t0001g0136 others(13): Show |
16 | NA18948.hp2 NA18952.hp1 NA18967.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+18402T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49024691 | |||||||
| chr13:49024751 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+18462A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49024751 | |||||||
| chr13:49024804 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0010t0004g0153 |
3 | HG01884.hp1 HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.99+18515T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49024804 | |||||||
| chr13:49024868 | C | T | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99+18579C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49024868 | |||||||
| chr13:49024946 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+18657G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49024946 | |||||||
| chr13:49025295 | C | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0146 |
2 | NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.99+19006C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49025295 | |||||||
| chr13:49025366 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+19077A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49025366 | |||||||
| chr13:49025399 | C | G | 1 | a0001c0001t0001g0179 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.99+19110C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49025399 | |||||||
| chr13:49025520 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+19231A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49025520 | |||||||
| chr13:49025577 | C | T | 1 | a0002c0003t0001g0002 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.99+19288C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49025577 | |||||||
| chr13:49025982 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.99+19693G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49025982 | |||||||
| chr13:49026075 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.99+19786A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49026075 | |||||||
| chr13:49026258 | G | A | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+19969G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49026258 | |||||||
| chr13:49026455 | T | C | 7 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(4): Show |
7 | HG00597.hp1 HG02523.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+20166T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49026455 | |||||||
| chr13:49026584 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.99+20295G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49026584 | |||||||
| chr13:49026631 | G | C | 5 | a0001c0001t0001g0193 a0001c0001t0001g0238 a0001c0001t0001g0268 others(2): Show |
5 | HG00438.hp1 HG01081.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+20342G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49026631 | |||||||
| chr13:49026633 | A | G | 5 | a0001c0001t0001g0193 a0001c0001t0001g0238 a0001c0001t0001g0268 others(2): Show |
5 | HG00438.hp1 HG01081.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+20344A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49026633 | |||||||
| chr13:49026715 | G | C | 8 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(5): Show |
8 | NA18612.hp2 NA18939.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+20426G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49026715 | |||||||
| chr13:49026930 | A | C | 1 | a0001c0002t0001g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99+20641A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49026930 | |||||||
| chr13:49027152 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+20863A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49027152 | |||||||
| chr13:49027227 | C | T | 2 | a0001c0001t0001g0115 a0001c0002t0001g0104 |
2 | NA18991.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.99+20938C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49027227 | |||||||
| chr13:49027228 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.99+20939G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49027228 | |||||||
| chr13:49027467 | T | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0159 |
2 | HG03017.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.99+21178T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49027467 | |||||||
| chr13:49027513 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.99+21224T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49027513 | |||||||
| chr13:49027594 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(149): Show |
152 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.99+21305A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49027594 | |||||||
| chr13:49027802 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.99+21513T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49027802 | |||||||
| chr13:49027814 | TA | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.99+21529delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49027814 | ||||||
| chr13:49028129 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.99+21840C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49028129 | |||||||
| chr13:49028255 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+21966A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49028255 | |||||||
| chr13:49028286 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.99+21997G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49028286 | |||||||
| chr13:49028332 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+22043C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49028332 | |||||||
| chr13:49028556 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.99+22267A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49028556 | |||||||
| chr13:49029000 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.99+22711G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49029000 | |||||||
| chr13:49029212 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.99+22923A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49029212 | |||||||
| chr13:49029319 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.99+23030G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49029319 | |||||||
| chr13:49029470 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+23181A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49029470 | |||||||
| chr13:49029598 | A | C | 1 | a0006c0006t0001g0074 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.99+23309A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49029598 | |||||||
| chr13:49029709 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.99+23420A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49029709 | |||||||
| chr13:49029988 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+23699T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49029988 | |||||||
| chr13:49030046 | T | G | 1 | a0001c0001t0001g0289 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.99+23757T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49030046 | |||||||
| chr13:49030111 | A | G | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.99+23822A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49030111 | |||||||
| chr13:49030246 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+23957A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49030246 | |||||||
| chr13:49030253 | A | T | 1 | a0001c0001t0001g0235 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.99+23964A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49030253 | |||||||
| chr13:49030398 | A | AC | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
13 | HG01167.hp2 HG01175.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+24110dupC | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49030398 | ||||||
| chr13:49030398 | A | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(272): Show |
275 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.99+24109A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49030398 | |||||||
| chr13:49030459 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.99+24170A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49030459 | |||||||
| chr13:49030496 | C | T | 4 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0223 others(1): Show |
4 | NA18959.hp1 NA18969.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+24207C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49030496 | |||||||
| chr13:49030625 | C | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+24336C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49030625 | |||||||
| chr13:49030712 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.99+24423C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49030712 | |||||||
| chr13:49031476 | C | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.99+25187C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49031476 | |||||||
| chr13:49031638 | A | G | 4 | a0001c0002t0001g0085 a0001c0002t0001g0119 a0001c0002t0001g0120 others(1): Show |
4 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+25349A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49031638 | |||||||
| chr13:49031677 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.99+25388C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49031677 | |||||||
| chr13:49031797 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.99+25508G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49031797 | |||||||
| chr13:49031868 | C | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.99+25579C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49031868 | |||||||
| chr13:49032033 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+25744A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032033 | |||||||
| chr13:49032151 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.99+25862C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032151 | |||||||
| chr13:49032166 | G | T | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.99+25877G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032166 | |||||||
| chr13:49032270 | A | G | 4 | a0001c0002t0001g0085 a0001c0002t0001g0119 a0001c0002t0001g0120 others(1): Show |
4 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+25981A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032270 | |||||||
| chr13:49032476 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+26187C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032476 | |||||||
| chr13:49032494 | C | T | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG01891.hp1 HG02698.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+26205C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032494 | |||||||
| chr13:49032650 | G | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+26361G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032650 | |||||||
| chr13:49032652 | C | T | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99+26363C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032652 | |||||||
| chr13:49032701 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.99+26412A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032701 | |||||||
| chr13:49032731 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+26442G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032731 | |||||||
| chr13:49032854 | T | C | 16 | a0001c0001t0001g0168 a0001c0001t0001g0245 a0001c0001t0001g0247 others(13): Show |
16 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+26565T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49032854 | |||||||
| chr13:49032897 | AT | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+26613delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49032897 | ||||||
| chr13:49033278 | T | C | 65 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(62): Show |
65 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.99+26989T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49033278 | |||||||
| chr13:49033331 | A | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+27042A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49033331 | |||||||
| chr13:49033417 | C | G | 1 | a0001c0002t0001g0113 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.99+27128C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49033417 | |||||||
| chr13:49033484 | G | T | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.99+27195G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49033484 | |||||||
| chr13:49033506 | A | G | 1 | a0002c0003t0001g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+27217A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49033506 | |||||||
| chr13:49033725 | A | G | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99+27436A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49033725 | |||||||
| chr13:49033789 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99+27500G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49033789 | |||||||
| chr13:49033866 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+27577A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49033866 | |||||||
| chr13:49034097 | C | T | 18 | a0001c0001t0001g0168 a0001c0001t0001g0245 a0001c0001t0001g0247 others(15): Show |
18 | HG00639.hp2 HG00741.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+27808C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034097 | |||||||
| chr13:49034111 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.99+27822T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034111 | |||||||
| chr13:49034169 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.99+27880A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034169 | |||||||
| chr13:49034173 | A | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.99+27884A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034173 | |||||||
| chr13:49034222 | C | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(149): Show |
152 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.99+27933C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034222 | |||||||
| chr13:49034494 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.99+28205G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034494 | |||||||
| chr13:49034529 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.99+28240C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034529 | |||||||
| chr13:49034545 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+28256C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034545 | |||||||
| chr13:49034603 | G | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+28314G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034603 | |||||||
| chr13:49034789 | G | T | 1 | a0001c0001t0001g0179 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.99+28500G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034789 | |||||||
| chr13:49034805 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18943.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.99+28516A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49034805 | |||||||
| chr13:49035188 | T | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
13 | HG01167.hp2 HG01175.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+28899T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49035188 | |||||||
| chr13:49035357 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+29068A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49035357 | |||||||
| chr13:49035467 | A | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.99+29178A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49035467 | |||||||
| chr13:49035498 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+29209A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49035498 | |||||||
| chr13:49035988 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99+29699G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49035988 | |||||||
| chr13:49036141 | T | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+29852T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49036141 | |||||||
| chr13:49036319 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.99+30030A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49036319 | |||||||
| chr13:49036411 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.99+30122A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49036411 | |||||||
| chr13:49036448 | T | G | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.99+30159T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49036448 | |||||||
| chr13:49036557 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.99+30268T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49036557 | |||||||
| chr13:49036700 | G | C | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+30411G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49036700 | |||||||
| chr13:49036914 | A | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.99+30625A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49036914 | |||||||
| chr13:49036986 | G | A | 118 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(115): Show |
118 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.99+30697G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49036986 | |||||||
| chr13:49037048 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+30759C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49037048 | |||||||
| chr13:49037252 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99+30963G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49037252 | |||||||
| chr13:49037569 | C | A | 1 | a0001c0001t0001g0266 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.99+31280C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49037569 | |||||||
| chr13:49037599 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.99+31310T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49037599 | |||||||
| chr13:49037708 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+31419A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49037708 | |||||||
| chr13:49037911 | T | C | 10 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0171 others(7): Show |
10 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+31622T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49037911 | |||||||
| chr13:49038009 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.99+31720C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49038009 | |||||||
| chr13:49038132 | G | A | 1 | a0001c0002t0001g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.99+31843G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49038132 | |||||||
| chr13:49038157 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+31868C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49038157 | |||||||
| chr13:49038307 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.99+32018G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49038307 | |||||||
| chr13:49038542 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+32253G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49038542 | |||||||
| chr13:49038661 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.99+32372A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49038661 | |||||||
| chr13:49038759 | G | A | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.99+32470G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49038759 | |||||||
| chr13:49038810 | C | T | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99+32521C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49038810 | |||||||
| chr13:49038848 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.99+32559C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49038848 | |||||||
| chr13:49039027 | C | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+32738C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49039027 | |||||||
| chr13:49039072 | C | T | 16 | a0001c0001t0001g0168 a0001c0001t0001g0245 a0001c0001t0001g0247 others(13): Show |
16 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+32783C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49039072 | |||||||
| chr13:49039421 | T | C | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.99+33132T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49039421 | |||||||
| chr13:49039745 | G | A | 1 | a0001c0001t0009g0202 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.99+33456G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49039745 | |||||||
| chr13:49039771 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG02145.hp1 HG02451.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+33482A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49039771 | |||||||
| chr13:49039776 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.99+33487G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49039776 | |||||||
| chr13:49039863 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.99+33574C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49039863 | |||||||
| chr13:49040041 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.99+33752G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49040041 | |||||||
| chr13:49040171 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0250 |
2 | HG00639.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.99+33882T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49040171 | |||||||
| chr13:49040374 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.99+34085C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49040374 | |||||||
| chr13:49040474 | A | G | 2 | a0002c0003t0001g0004 a0002c0003t0001g0005 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.99+34185A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49040474 | |||||||
| chr13:49040484 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.99+34195A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49040484 | |||||||
| chr13:49040521 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+34232T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49040521 | |||||||
| chr13:49040615 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+34326A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49040615 | |||||||
| chr13:49040968 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-34321C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49040968 | |||||||
| chr13:49041134 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.100-34155G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49041134 | |||||||
| chr13:49041203 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-34086T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49041203 | |||||||
| chr13:49041377 | T | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-33912T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49041377 | |||||||
| chr13:49041381 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-33908A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49041381 | |||||||
| chr13:49041381 | A | T | 4 | a0003c0004t0001g0028 a0003c0004t0001g0031 a0003c0004t0001g0035 others(1): Show |
4 | HG00280.hp2 HG01515.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-33908A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49041381 | |||||||
| chr13:49041813 | C | CA | 17 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(14): Show |
17 | HG01074.hp2 HG01243.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-33459dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49041813 | ||||||
| chr13:49041882 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.100-33407A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49041882 | |||||||
| chr13:49041956 | C | T | 1 | a0001c0001t0009g0202 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.100-33333C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49041956 | |||||||
| chr13:49042107 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-33182C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49042107 | |||||||
| chr13:49042183 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.100-33106T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49042183 | |||||||
| chr13:49042293 | A | AT | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-32990dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49042293 | ||||||
| chr13:49042697 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00621.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.100-32592A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49042697 | |||||||
| chr13:49042739 | T | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-32550T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49042739 | |||||||
| chr13:49042829 | C | T | 4 | a0001c0001t0001g0212 a0001c0001t0001g0233 a0001c0001t0001g0241 others(1): Show |
4 | HG02074.hp1 HG02132.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-32460C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49042829 | |||||||
| chr13:49043122 | G | GT | 17 | a0001c0001t0001g0124 a0001c0001t0001g0128 a0001c0001t0001g0129 others(14): Show |
17 | HG01074.hp2 HG01975.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-32151dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49043122 | ||||||
| chr13:49043127 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100-32162T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49043127 | |||||||
| chr13:49043168 | G | GT | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.100-32119dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49043168 | ||||||
| chr13:49043258 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.100-32031C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49043258 | |||||||
| chr13:49043591 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.100-31698A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49043591 | |||||||
| chr13:49043696 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.100-31593A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49043696 | |||||||
| chr13:49043698 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-31591A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49043698 | |||||||
| chr13:49043855 | TTAAA | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-31427_100-3142 others(8): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49043855 | ||||||
| chr13:49043987 | C | T | 7 | a0001c0001t0001g0217 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | HG01433.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-31302C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49043987 | |||||||
| chr13:49044274 | C | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG02818.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-31015C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49044274 | |||||||
| chr13:49044291 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.100-30998A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49044291 | |||||||
| chr13:49044393 | C | T | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.100-30896C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49044393 | |||||||
| chr13:49044496 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.100-30793C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49044496 | |||||||
| chr13:49045031 | CTTTCCTT others(5): Show |
C | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-30243_100-3023 others(16): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49045031 | ||||||
| chr13:49045034 | TCCTTTCC others(11): Show |
T | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.100-30225_100-3020 others(22): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49045034 | ||||||
| chr13:49045043 | TTTTCCTT others(28): Show |
T | 1 | a0001c0001t0001g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.100-30225_100-3019 others(39): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49045043 | ||||||
| chr13:49045099 | G | C | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.100-30190G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49045099 | |||||||
| chr13:49045099 | GCCTTTCC others(23): Show |
G | 1 | a0001c0001t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.100-30173_100-3014 others(34): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49045099 | ||||||
| chr13:49045123 | C | CCCTTTCC others(10): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0287 |
2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.100-30141_100-3012 others(21): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49045123 | ||||||
| chr13:49045185 | ACT | A | 25 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
25 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.100-30101_100-3010 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49045185 | ||||||
| chr13:49045305 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.100-29984C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49045305 | |||||||
| chr13:49045611 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100-29678G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49045611 | |||||||
| chr13:49045714 | T | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0242 |
3 | HG02630.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.100-29575T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49045714 | |||||||
| chr13:49045790 | CT | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(238): Show |
241 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.100-29480delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49045790 | ||||||
| chr13:49045790 | CTT | C | 8 | a0001c0001t0001g0039 a0001c0001t0001g0068 a0001c0001t0001g0130 others(5): Show |
8 | HG00438.hp1 HG01070.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-29481_100-2948 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49045790 | ||||||
| chr13:49045894 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-29395A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49045894 | |||||||
| chr13:49045915 | G | A | 1 | a0002c0003t0001g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-29374G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49045915 | |||||||
| chr13:49046090 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(149): Show |
152 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.100-29199C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49046090 | |||||||
| chr13:49046517 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.100-28772A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49046517 | |||||||
| chr13:49046529 | C | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-28760C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49046529 | |||||||
| chr13:49046576 | T | G | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG02132.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.100-28713T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49046576 | |||||||
| chr13:49046590 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-28699T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49046590 | |||||||
| chr13:49046720 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-28569C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49046720 | |||||||
| chr13:49046721 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.100-28568C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49046721 | |||||||
| chr13:49046723 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.100-28566A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49046723 | |||||||
| chr13:49046853 | G | GT | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.100-28426dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49046853 | ||||||
| chr13:49047146 | AT | A | 29 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0075 others(26): Show |
29 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.100-28130delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49047146 | ||||||
| chr13:49047149 | T | A | 2 | a0002c0003t0001g0004 a0002c0003t0001g0005 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.100-28140T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49047149 | |||||||
| chr13:49047306 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01074.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-27983A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49047306 | |||||||
| chr13:49047314 | C | T | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-27975C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49047314 | |||||||
| chr13:49047480 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-27809A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49047480 | |||||||
| chr13:49047767 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.100-27522C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49047767 | |||||||
| chr13:49047820 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.100-27469A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49047820 | |||||||
| chr13:49048483 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.100-26806T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49048483 | |||||||
| chr13:49048859 | A | G | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.100-26430A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49048859 | |||||||
| chr13:49048934 | A | G | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.100-26355A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49048934 | |||||||
| chr13:49049321 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.100-25968A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49049321 | |||||||
| chr13:49049466 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.100-25823T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49049466 | |||||||
| chr13:49049703 | CTTCTT | C | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.100-25573_100-2556 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49049703 | ||||||
| chr13:49050008 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-25281C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49050008 | |||||||
| chr13:49050034 | C | T | 2 | a0001c0001t0001g0115 a0001c0002t0001g0104 |
2 | NA18991.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.100-25255C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49050034 | |||||||
| chr13:49050174 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.100-25115C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49050174 | |||||||
| chr13:49050211 | C | G | 5 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-25078C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49050211 | |||||||
| chr13:49050215 | G | A | 5 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-25074G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49050215 | |||||||
| chr13:49050241 | G | A | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.100-25048G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49050241 | |||||||
| chr13:49050672 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.100-24617A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49050672 | |||||||
| chr13:49050886 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0261 |
2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.100-24403A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49050886 | |||||||
| chr13:49050901 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.100-24388T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49050901 | |||||||
| chr13:49051393 | T | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.100-23896T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49051393 | |||||||
| chr13:49051565 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-23724T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49051565 | |||||||
| chr13:49051994 | C | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-23295C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49051994 | |||||||
| chr13:49052559 | C | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.100-22730C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49052559 | |||||||
| chr13:49052656 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.100-22633C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49052656 | |||||||
| chr13:49052685 | A | G | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.100-22604A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49052685 | |||||||
| chr13:49052695 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.100-22594G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49052695 | |||||||
| chr13:49052855 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.100-22434T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49052855 | |||||||
| chr13:49052951 | G | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | NA18956.hp1 NA18968.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.100-22338G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49052951 | |||||||
| chr13:49053011 | A | C | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.100-22278A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49053011 | |||||||
| chr13:49053064 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.100-22225A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49053064 | |||||||
| chr13:49053091 | C | T | 1 | a0002c0003t0001g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100-22198C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49053091 | |||||||
| chr13:49053304 | C | G | 4 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0246 others(1): Show |
4 | NA18953.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-21985C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49053304 | |||||||
| chr13:49053405 | A | G | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.100-21884A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49053405 | |||||||
| chr13:49053672 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-21617G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49053672 | |||||||
| chr13:49053718 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-21571G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49053718 | |||||||
| chr13:49053720 | C | T | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.100-21569C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49053720 | |||||||
| chr13:49053754 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-21535T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49053754 | |||||||
| chr13:49053805 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-21484A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49053805 | |||||||
| chr13:49054145 | T | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(134): Show |
137 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.100-21144T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49054145 | |||||||
| chr13:49054287 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-21002A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49054287 | |||||||
| chr13:49054415 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.100-20874A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49054415 | |||||||
| chr13:49054552 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.100-20737C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49054552 | |||||||
| chr13:49054572 | T | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.100-20717T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49054572 | |||||||
| chr13:49054723 | G | A | 48 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(45): Show |
48 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.100-20566G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49054723 | |||||||
| chr13:49054770 | G | C | 114 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(111): Show |
114 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.100-20519G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49054770 | |||||||
| chr13:49054980 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.100-20309C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49054980 | |||||||
| chr13:49055110 | T | C | 1 | a0001c0001t0010g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.100-20179T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055110 | |||||||
| chr13:49055126 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-20163C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055126 | |||||||
| chr13:49055158 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-20131C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055158 | |||||||
| chr13:49055159 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.100-20130G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055159 | |||||||
| chr13:49055282 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.100-20007T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055282 | |||||||
| chr13:49055390 | T | G | 1 | a0001c0001t0001g0290 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.100-19899T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055390 | |||||||
| chr13:49055395 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.100-19894C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055395 | |||||||
| chr13:49055413 | G | A | 16 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(13): Show |
16 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-19876G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055413 | |||||||
| chr13:49055420 | G | A | 7 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
7 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-19869G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055420 | |||||||
| chr13:49055492 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.100-19797C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055492 | |||||||
| chr13:49055504 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-19785C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055504 | |||||||
| chr13:49055515 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-19774A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055515 | |||||||
| chr13:49055529 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(141): Show |
144 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.100-19760T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055529 | |||||||
| chr13:49055572 | G | C | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.100-19717G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055572 | |||||||
| chr13:49055595 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-19694C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055595 | |||||||
| chr13:49055658 | A | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-19631A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055658 | |||||||
| chr13:49055889 | T | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-19400T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055889 | |||||||
| chr13:49055898 | T | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-19391T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055898 | |||||||
| chr13:49055938 | G | C | 1 | a0001c0002t0001g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.100-19351G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49055938 | |||||||
| chr13:49056038 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.100-19251T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49056038 | |||||||
| chr13:49056186 | C | CA | 22 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0079 others(19): Show |
22 | HG01106.hp1 HG01243.hp2 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.100-19089dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49056186 | ||||||
| chr13:49056186 | CA | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
7 | HG01257.hp1 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-19089delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49056186 | ||||||
| chr13:49056257 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.100-19032A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49056257 | |||||||
| chr13:49056349 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-18940A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49056349 | |||||||
| chr13:49056424 | A | C | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.100-18865A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49056424 | |||||||
| chr13:49056708 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.100-18581T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49056708 | |||||||
| chr13:49056812 | A | C | 1 | a0001c0001t0001g0026 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.100-18477A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49056812 | |||||||
| chr13:49056999 | G | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG02698.hp2 HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.100-18290G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49056999 | |||||||
| chr13:49057219 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.100-18070T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49057219 | |||||||
| chr13:49057230 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.100-18059A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49057230 | |||||||
| chr13:49057248 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-18041T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49057248 | |||||||
| chr13:49057478 | T | C | 16 | a0001c0001t0001g0168 a0001c0001t0001g0245 a0001c0001t0001g0247 others(13): Show |
16 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-17811T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49057478 | |||||||
| chr13:49057733 | A | AGCATATA others(10): Show |
1 | a0001c0001t0001g0227 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.100-17553_100-1753 others(21): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49057733 | ||||||
| chr13:49057802 | T | TTTTTGTT others(46): Show |
1 | a0003c0004t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.100-17484_100-1748 others(57): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49057802 | ||||||
| chr13:49058121 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0099 others(2): Show |
5 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-17168C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49058121 | |||||||
| chr13:49058123 | G | A | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.100-17166G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49058123 | |||||||
| chr13:49058146 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.100-17143C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49058146 | |||||||
| chr13:49058359 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.100-16930C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49058359 | |||||||
| chr13:49058365 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.100-16924A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49058365 | |||||||
| chr13:49058614 | A | T | 1 | a0001c0002t0001g0090 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.100-16675A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49058614 | |||||||
| chr13:49058735 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-16554C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49058735 | |||||||
| chr13:49059151 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG00438.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.100-16138C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49059151 | |||||||
| chr13:49059267 | A | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-16022A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49059267 | |||||||
| chr13:49059412 | G | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-15877G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49059412 | |||||||
| chr13:49059483 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.100-15806T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49059483 | |||||||
| chr13:49059498 | C | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01074.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-15791C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49059498 | |||||||
| chr13:49059573 | A | C | 1 | a0001c0002t0001g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.100-15716A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49059573 | |||||||
| chr13:49059751 | C | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0066 a0006c0006t0001g0074 |
3 | NA18951.hp2 NA18962.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.100-15538C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49059751 | |||||||
| chr13:49060005 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.100-15284A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49060005 | |||||||
| chr13:49060037 | AATCCTTA others(3): Show |
A | 1 | a0001c0001t0001g0046 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.100-15249_100-1524 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49060037 | ||||||
| chr13:49060286 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.100-15003C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49060286 | |||||||
| chr13:49060407 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.100-14882G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49060407 | |||||||
| chr13:49060441 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-14848C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49060441 | |||||||
| chr13:49060643 | C | CA | 14 | a0001c0001t0001g0062 a0001c0001t0001g0124 a0001c0001t0001g0129 others(11): Show |
14 | HG02886.hp2 HG03195.hp2 HG03209.hp1 others(11): Show |
intron_variant | MODIFIER | c.100-14620dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49060643 | ||||||
| chr13:49060643 | CA | C | 124 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(121): Show |
124 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.100-14620delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49060643 | ||||||
| chr13:49060643 | CAA | C | 95 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0164 others(92): Show |
95 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.100-14621_100-1462 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49060643 | ||||||
| chr13:49060715 | C | G | 6 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
6 | HG01433.hp2 HG01934.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-14574C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49060715 | |||||||
| chr13:49060793 | A | G | 106 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(103): Show |
106 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.100-14496A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49060793 | |||||||
| chr13:49061017 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.100-14272T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061017 | |||||||
| chr13:49061203 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.100-14086G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061203 | |||||||
| chr13:49061307 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13982T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061307 | |||||||
| chr13:49061309 | C | T | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13980C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061309 | |||||||
| chr13:49061313 | T | TCTTTTCC | 4 | a0001c0001t0001g0188 a0001c0001t0001g0205 a0001c0001t0001g0209 others(1): Show |
4 | NA18982.hp1 NA18983.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-13973_100-1397 others(11): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061313 | ||||||
| chr13:49061318 | T | C | 4 | a0001c0001t0001g0188 a0001c0001t0001g0205 a0001c0001t0001g0209 others(1): Show |
4 | NA18982.hp1 NA18983.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-13971T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061318 | |||||||
| chr13:49061318 | T | TCTTCCCT others(3): Show |
4 | a0001c0001t0001g0160 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG02922.hp1 NA18956.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-13942_100-1393 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061318 | ||||||
| chr13:49061318 | T | TCTTCCCT others(8): Show |
2 | a0001c0001t0001g0008 a0001c0001t0006g0161 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-13947_100-1393 others(19): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061318 | ||||||
| chr13:49061318 | T | TCTTCCCT others(28): Show |
1 | a0001c0005t0001g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100-13967_100-1393 others(39): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061318 | ||||||
| chr13:49061318 | T | TCTTCCCT others(63): Show |
1 | a0001c0005t0001g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.100-13933_100-1393 others(74): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061318 | ||||||
| chr13:49061318 | T | TCTTCTCT others(3): Show |
1 | a0001c0001t0001g0263 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-13967_100-1396 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061318 | ||||||
| chr13:49061318 | T | TCTTCTCT others(8): Show |
1 | a0001c0001t0001g0229 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.100-13967_100-1396 others(19): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061318 | ||||||
| chr13:49061319 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.100-13970C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061319 | |||||||
| chr13:49061320 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13969T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061320 | |||||||
| chr13:49061323 | C | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG02698.hp1 HG03831.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.100-13966C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061323 | |||||||
| chr13:49061327 | CCCTTCCC others(23): Show |
C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0288 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.100-13932_100-1390 others(34): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061327 | ||||||
| chr13:49061332 | CCCTTCCC others(18): Show |
C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(1): Show |
4 | HG03453.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-13932_100-1390 others(29): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061332 | ||||||
| chr13:49061337 | CCCTTCCC others(13): Show |
C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0154 others(1): Show |
4 | HG02886.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-13932_100-1391 others(24): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061337 | ||||||
| chr13:49061342 | CCCTTCCC others(8): Show |
C | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
54 | HG00408.hp1 HG00639.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.100-13932_100-1391 others(19): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061342 | ||||||
| chr13:49061347 | CCCTTCCC others(3): Show |
C | 69 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(66): Show |
69 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.100-13932_100-1392 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061347 | ||||||
| chr13:49061352 | CCCTTA | C | 19 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0029 others(16): Show |
19 | HG01167.hp1 HG01169.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.100-13932_100-1392 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061352 | ||||||
| chr13:49061357 | A | C | 137 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0032 others(134): Show |
137 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.100-13932A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061357 | |||||||
| chr13:49061357 | A | T | 1 | a0001c0001t0001g0059 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.100-13932A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061357 | |||||||
| chr13:49061370 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.100-13919T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061370 | |||||||
| chr13:49061371 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-13918T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061371 | |||||||
| chr13:49061376 | T | C | 5 | a0001c0001t0001g0114 a0001c0001t0001g0142 a0001c0001t0001g0157 others(2): Show |
5 | HG02451.hp1 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-13913T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061376 | |||||||
| chr13:49061381 | T | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0106 a0001c0001t0008g0051 others(1): Show |
4 | HG03130.hp2 NA18972.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-13908T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061381 | |||||||
| chr13:49061385 | T | C | 1 | a0001c0002t0001g0090 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.100-13904T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061385 | |||||||
| chr13:49061386 | T | C | 157 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(154): Show |
157 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.100-13903T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061386 | |||||||
| chr13:49061386 | T | TCCCTC | 68 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(65): Show |
68 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.100-13899_100-1389 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061386 | ||||||
| chr13:49061387 | C | T | 1 | a0001c0002t0001g0090 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.100-13902C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061387 | |||||||
| chr13:49061391 | T | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0106 others(16): Show |
19 | HG01081.hp2 HG01975.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.100-13898T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061391 | |||||||
| chr13:49061396 | C | T | 9 | a0001c0001t0001g0127 a0001c0001t0001g0184 a0001c0001t0001g0226 others(6): Show |
9 | HG02109.hp1 HG02698.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-13893C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061396 | |||||||
| chr13:49061399 | C | CTCCCCTC others(13): Show |
1 | a0001c0001t0001g0025 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.100-13889_100-1388 others(24): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061399 | ||||||
| chr13:49061399 | C | CTCCCCTC others(3): Show |
1 | a0001c0001t0001g0142 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.100-13889_100-1388 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061399 | ||||||
| chr13:49061399 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-13890C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061399 | |||||||
| chr13:49061401 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(248): Show |
251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.100-13888T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061401 | |||||||
| chr13:49061402 | C | CCTCCTTC others(8): Show |
1 | a0001c0001t0001g0227 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.100-13886_100-1388 others(19): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061402 | ||||||
| chr13:49061404 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.100-13885C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061404 | |||||||
| chr13:49061406 | C | T | 7 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(4): Show |
7 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-13883C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061406 | |||||||
| chr13:49061412 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.100-13877C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061412 | |||||||
| chr13:49061414 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0008g0051 a0001c0002t0001g0090 |
3 | NA18972.hp1 NA18973.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.100-13875C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061414 | |||||||
| chr13:49061419 | C | CTCCCCTC others(3): Show |
26 | a0001c0001t0001g0128 a0001c0001t0001g0162 a0001c0001t0001g0180 others(23): Show |
26 | HG00544.hp2 HG00597.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.100-13861_100-1386 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061419 | ||||||
| chr13:49061419 | C | CTCCCT | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-13866_100-1386 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061419 | ||||||
| chr13:49061419 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(235): Show |
238 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.100-13870C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061419 | |||||||
| chr13:49061420 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.100-13869T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061420 | |||||||
| chr13:49061421 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.100-13868C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061421 | |||||||
| chr13:49061423 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-13866C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061423 | |||||||
| chr13:49061424 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0129 |
2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.100-13865C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061424 | |||||||
| chr13:49061425 | T | TCCCTTCC others(4): Show |
1 | a0001c0001t0001g0168 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.100-13861_100-1386 others(15): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061425 | ||||||
| chr13:49061426 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.100-13863C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061426 | |||||||
| chr13:49061434 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-13855C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061434 | |||||||
| chr13:49061438 | CCTT | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0008g0051 |
3 | HG02976.hp1 HG03130.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.100-13848_100-1384 others(7): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061438 | ||||||
| chr13:49061440 | T | TTCTCCCC others(65): Show |
15 | a0001c0001t0001g0168 a0001c0001t0001g0245 a0001c0001t0001g0247 others(12): Show |
15 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-13825_100-1382 others(76): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061440 | ||||||
| chr13:49061452 | T | C | 4 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0001g0136 others(1): Show |
4 | HG02976.hp1 HG03130.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-13837T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061452 | |||||||
| chr13:49061455 | C | CCCTCCCC others(8): Show |
1 | a0002c0003t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.100-13786_100-1377 others(19): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061455 | ||||||
| chr13:49061455 | C | CCCTCCCC others(8): Show |
2 | a0001c0001t0001g0197 a0001c0001t0001g0262 |
2 | HG02895.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.100-13825_100-1382 others(19): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061455 | ||||||
| chr13:49061455 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-13834C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061455 | |||||||
| chr13:49061455 | CCCTCCCC others(8): Show |
C | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.100-13786_100-1377 others(19): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061455 | ||||||
| chr13:49061459 | CCCCTCCC others(7): Show |
C | 1 | a0001c0001t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.100-13826_100-1381 others(18): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061459 | ||||||
| chr13:49061460 | CCCTCCCC others(3): Show |
C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0132 a0001c0001t0001g0133 others(5): Show |
8 | HG01975.hp2 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-13819_100-1381 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061460 | ||||||
| chr13:49061465 | C | T | 122 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(119): Show |
122 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.100-13824C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061465 | |||||||
| chr13:49061467 | C | T | 1 | a0001c0001t0008g0051 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.100-13822C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061467 | |||||||
| chr13:49061470 | T | C | 1 | a0001c0001t0008g0051 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.100-13819T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061470 | |||||||
| chr13:49061480 | C | T | 2 | a0001c0001t0001g0192 a0004c0007t0001g0191 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.100-13809C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061480 | |||||||
| chr13:49061493 | TCCCCTCT others(9): Show |
T | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.100-13792_100-1377 others(20): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061493 | ||||||
| chr13:49061497 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-13792C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061497 | |||||||
| chr13:49061500 | T | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0001g0136 |
3 | HG02976.hp1 HG03130.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.100-13789T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061500 | |||||||
| chr13:49061512 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-13777C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061512 | |||||||
| chr13:49061512 | CT | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.100-13776delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061512 | |||||||
| chr13:49061524 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-13765T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061524 | |||||||
| chr13:49061525 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13764T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061525 | |||||||
| chr13:49061527 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-13762C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061527 | |||||||
| chr13:49061528 | C | T | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13761C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061528 | |||||||
| chr13:49061538 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.100-13751C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061538 | |||||||
| chr13:49061539 | C | T | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13750C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061539 | |||||||
| chr13:49061540 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13749T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061540 | |||||||
| chr13:49061541 | T | C | 4 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0001g0259 others(1): Show |
4 | HG01934.hp2 HG02897.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-13748T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061541 | |||||||
| chr13:49061541 | T | TCTCCCCT others(8): Show |
3 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0154 |
3 | HG01074.hp2 HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.100-13714_100-1370 others(19): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061541 | ||||||
| chr13:49061545 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-13744C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061545 | |||||||
| chr13:49061555 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13734T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061555 | |||||||
| chr13:49061560 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-13729C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061560 | |||||||
| chr13:49061570 | T | C | 5 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0005 others(2): Show |
5 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-13719T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061570 | |||||||
| chr13:49061571 | C | CCTCCCCT others(33): Show |
1 | a0001c0001t0001g0259 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.100-13702_100-1370 others(44): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061571 | ||||||
| chr13:49061580 | CCCTCT | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-13699_100-1369 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061580 | ||||||
| chr13:49061581 | C | A | 1 | a0001c0001t0001g0206 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.100-13708C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061581 | |||||||
| chr13:49061581 | C | T | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13708C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061581 | |||||||
| chr13:49061582 | C | T | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13707C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061582 | |||||||
| chr13:49061583 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13706T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061583 | |||||||
| chr13:49061588 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13701T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061588 | |||||||
| chr13:49061590 | T | C | 2 | a0001c0001t0001g0259 a0001c0010t0004g0153 |
2 | HG01891.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.100-13699T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061590 | |||||||
| chr13:49061596 | C | T | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13693C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061596 | |||||||
| chr13:49061598 | TCTCCTCC others(28): Show |
T | 1 | a0001c0001t0001g0136 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.100-13689_100-1365 others(39): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061598 | ||||||
| chr13:49061600 | TCCTCC | T | 3 | a0001c0001t0002g0171 a0001c0005t0001g0155 a0001c0005t0001g0156 |
3 | HG00741.hp2 NA18906.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.100-13679_100-1367 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061600 | ||||||
| chr13:49061605 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.100-13684C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061605 | |||||||
| chr13:49061613 | TCTCCCCT others(22): Show |
T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.100-13658_100-1363 others(33): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061613 | ||||||
| chr13:49061619 | C | CTCCCCTC others(5): Show |
1 | a0001c0002t0001g0107 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.100-13658_100-1364 others(16): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061619 | ||||||
| chr13:49061625 | TCTCCCTT others(10): Show |
T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-13658_100-1364 others(21): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061625 | ||||||
| chr13:49061631 | T | C | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0215 others(3): Show |
6 | HG00639.hp2 HG01884.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-13658T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061631 | |||||||
| chr13:49061631 | TTCCCCTC others(22): Show |
T | 1 | a0001c0001t0001g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.100-13638_100-1361 others(33): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061631 | ||||||
| chr13:49061633 | C | CCCTCTCC others(3): Show |
1 | a0001c0002t0001g0090 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.100-13654_100-1365 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061633 | ||||||
| chr13:49061637 | T | TCCCCTCT others(3): Show |
1 | a0001c0001t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.100-13651_100-1365 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061637 | ||||||
| chr13:49061637 | TCTCCC | T | 121 | a0001c0001t0001g0008 a0001c0001t0001g0162 a0001c0001t0001g0163 others(118): Show |
121 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.100-13638_100-1363 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061637 | ||||||
| chr13:49061639 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.100-13650T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061639 | |||||||
| chr13:49061642 | C | CCTCCCCT others(5): Show |
4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG01975.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-13585_100-1357 others(16): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061642 | ||||||
| chr13:49061642 | C | CCTCCCCT others(12): Show |
2 | a0001c0001t0001g0197 a0001c0001t0001g0212 |
2 | HG02895.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.100-13639_100-1363 others(23): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061642 | ||||||
| chr13:49061642 | C | CCTCCCCT others(5): Show |
2 | a0001c0001t0001g0125 a0005c0008t0001g0123 |
2 | HG01257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.100-13639_100-1363 others(16): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061642 | ||||||
| chr13:49061642 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.100-13647C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061642 | |||||||
| chr13:49061642 | CCTCCCCT others(5): Show |
C | 6 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0157 others(3): Show |
6 | HG01074.hp2 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-13585_100-1357 others(16): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061642 | ||||||
| chr13:49061643 | C | T | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13646C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061643 | |||||||
| chr13:49061644 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13645T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061644 | |||||||
| chr13:49061645 | C | T | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13644C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061645 | |||||||
| chr13:49061648 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.100-13641C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061648 | |||||||
| chr13:49061651 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.100-13638C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061651 | |||||||
| chr13:49061656 | T | TCCCCTCC others(30): Show |
1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.100-13618_100-1361 others(41): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061656 | ||||||
| chr13:49061678 | TCTCCC | T | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(109): Show |
112 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.100-13602_100-1359 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061678 | ||||||
| chr13:49061680 | T | C | 1 | a0001c0002t0001g0090 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.100-13609T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061680 | |||||||
| chr13:49061683 | C | CCTCTCCC others(19): Show |
1 | a0001c0001t0001g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.100-13603_100-1360 others(30): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061683 | ||||||
| chr13:49061683 | C | T | 1 | a0001c0002t0001g0090 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.100-13606C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061683 | |||||||
| chr13:49061687 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0046 |
2 | NA18972.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.100-13602C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061687 | |||||||
| chr13:49061690 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0046 |
2 | NA18972.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.100-13599T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061690 | |||||||
| chr13:49061690 | TCTCCCCT others(2): Show |
T | 4 | a0001c0001t0001g0184 a0001c0001t0001g0211 a0001c0001t0001g0275 others(1): Show |
4 | HG01071.hp1 HG01515.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-13597_100-1358 others(13): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061690 | ||||||
| chr13:49061699 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0046 |
2 | NA18972.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.100-13590C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061699 | |||||||
| chr13:49061700 | CCT | C | 31 | a0001c0001t0001g0168 a0001c0001t0001g0190 a0001c0001t0001g0215 others(28): Show |
31 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.100-13585_100-1358 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061700 | ||||||
| chr13:49061702 | T | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0184 others(3): Show |
6 | HG01071.hp1 HG01515.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-13587T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061702 | |||||||
| chr13:49061702 | T | TCCC | 77 | a0001c0001t0001g0127 a0001c0001t0001g0162 a0001c0001t0001g0163 others(74): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.100-13586_100-1358 others(7): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061702 | ||||||
| chr13:49061702 | TCTCCC | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0066 a0001c0010t0004g0153 others(1): Show |
4 | HG01891.hp2 NA18951.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-13563_100-1355 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061702 | ||||||
| chr13:49061704 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0227 a0001c0001t0006g0161 others(1): Show |
4 | HG02145.hp1 HG02897.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-13585T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061704 | |||||||
| chr13:49061707 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0227 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG03471.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.100-13582C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061707 | |||||||
| chr13:49061709 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13580T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061709 | |||||||
| chr13:49061710 | C | T | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13579C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061710 | |||||||
| chr13:49061712 | C | CCTCTCCC others(7): Show |
1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.100-13574_100-1357 others(18): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061712 | ||||||
| chr13:49061712 | C | CT | 3 | a0001c0001t0001g0008 a0001c0001t0001g0227 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG03471.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.100-13577_100-1357 others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061712 | |||||||
| chr13:49061713 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.100-13576C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061713 | |||||||
| chr13:49061714 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.100-13575T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061714 | |||||||
| chr13:49061715 | C | CT | 3 | a0001c0001t0001g0136 a0001c0001t0001g0229 a0001c0001t0007g0225 |
3 | NA18954.hp2 NA18973.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.100-13574_100-1357 others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061715 | |||||||
| chr13:49061715 | C | CTCCCTCT others(5): Show |
1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-13574_100-1357 others(16): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061715 | |||||||
| chr13:49061716 | C | T | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13573C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061716 | |||||||
| chr13:49061717 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0227 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG03471.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.100-13572C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061717 | |||||||
| chr13:49061719 | T | C | 1 | a0002c0003t0001g0004 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.100-13570T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061719 | |||||||
| chr13:49061719 | TC | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0227 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG03471.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.100-13566delC | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061719 | ||||||
| chr13:49061720 | C | CT | 96 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(93): Show |
96 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.100-13569_100-1356 others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061720 | |||||||
| chr13:49061720 | C | CTCCCTCT others(5): Show |
2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.100-13569_100-1356 others(16): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061720 | |||||||
| chr13:49061720 | C | CTCCTCT | 3 | a0001c0001t0001g0127 a0001c0001t0001g0229 a0001c0001t0007g0225 |
3 | HG02109.hp1 NA18954.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.100-13569_100-1356 others(10): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061720 | |||||||
| chr13:49061720 | C | T | 2 | a0001c0001t0001g0235 a0002c0003t0001g0004 |
2 | HG02897.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.100-13569C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061720 | |||||||
| chr13:49061726 | C | CCCTCCCC others(9): Show |
6 | a0001c0001t0001g0197 a0001c0001t0001g0212 a0001c0001t0001g0224 others(3): Show |
6 | HG02074.hp1 HG02132.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-13559_100-1355 others(20): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061726 | ||||||
| chr13:49061726 | C | T | 107 | a0001c0001t0001g0008 a0001c0001t0001g0127 a0001c0001t0001g0162 others(104): Show |
107 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.100-13563C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061726 | |||||||
| chr13:49061743 | C | CCCTCT | 101 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(98): Show |
101 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.100-13538_100-1353 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061743 | ||||||
| chr13:49061743 | C | CCCTCTCC others(9): Show |
11 | a0001c0001t0001g0160 a0001c0001t0001g0217 a0001c0001t0001g0219 others(8): Show |
11 | HG00639.hp2 HG01070.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-13503_100-1348 others(20): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061743 | ||||||
| chr13:49061743 | C | CCCTCTCC others(25): Show |
3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0242 |
3 | HG02630.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.100-13519_100-1348 others(36): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061743 | ||||||
| chr13:49061743 | C | CCCTCTCC others(14): Show |
2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG00408.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.100-13534_100-1353 others(25): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061743 | ||||||
| chr13:49061743 | C | CCTCTCCC others(3): Show |
3 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0007g0225 |
3 | NA18953.hp2 NA18954.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.100-13545_100-1354 others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061743 | ||||||
| chr13:49061743 | C | CTCTCTCC others(14): Show |
1 | a0001c0001t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-13546_100-1354 others(25): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061743 | |||||||
| chr13:49061743 | CCCTCTCC others(9): Show |
C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-13503_100-1348 others(20): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061743 | ||||||
| chr13:49061756 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.100-13533C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061756 | |||||||
| chr13:49061802 | T | TCTCTC | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.100-13465_100-1346 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061802 | ||||||
| chr13:49061802 | TCTCTC | T | 6 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0003c0004t0001g0028 others(3): Show |
6 | HG00280.hp2 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-13465_100-1346 others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49061802 | ||||||
| chr13:49061817 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.100-13472C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061817 | |||||||
| chr13:49061823 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.100-13466C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49061823 | |||||||
| chr13:49062237 | C | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-13052C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49062237 | |||||||
| chr13:49062238 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.100-13051G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49062238 | |||||||
| chr13:49062676 | C | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-12613C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49062676 | |||||||
| chr13:49063359 | TA | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG02818.hp1 HG02886.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-11926delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49063359 | ||||||
| chr13:49063360 | A | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-11929A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063360 | |||||||
| chr13:49063462 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11827T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063462 | |||||||
| chr13:49063472 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11817G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063472 | |||||||
| chr13:49063479 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11810G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063479 | |||||||
| chr13:49063483 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11806T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063483 | |||||||
| chr13:49063488 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11801T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063488 | |||||||
| chr13:49063489 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11800T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063489 | |||||||
| chr13:49063490 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11799G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063490 | |||||||
| chr13:49063491 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11798C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063491 | |||||||
| chr13:49063493 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11796C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063493 | |||||||
| chr13:49063495 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11794G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063495 | |||||||
| chr13:49063496 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11793A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063496 | |||||||
| chr13:49063504 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11785C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063504 | |||||||
| chr13:49063507 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11782C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063507 | |||||||
| chr13:49063522 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11767A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063522 | |||||||
| chr13:49063535 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11754G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063535 | |||||||
| chr13:49063540 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11749G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063540 | |||||||
| chr13:49063557 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11732A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063557 | |||||||
| chr13:49063562 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11727G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063562 | |||||||
| chr13:49063563 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11726T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063563 | |||||||
| chr13:49063564 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11725T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063564 | |||||||
| chr13:49063567 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11722C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063567 | |||||||
| chr13:49063570 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11719G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063570 | |||||||
| chr13:49063571 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11718A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063571 | |||||||
| chr13:49063597 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100-11692G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063597 | |||||||
| chr13:49063606 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11683T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063606 | |||||||
| chr13:49063607 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11682A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063607 | |||||||
| chr13:49063619 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.100-11670G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063619 | |||||||
| chr13:49063631 | C | CCTAGAGA others(32): Show |
1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11657_100-1165 others(43): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49063631 | ||||||
| chr13:49063639 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11650A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063639 | |||||||
| chr13:49063654 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11635G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063654 | |||||||
| chr13:49063666 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11623C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063666 | |||||||
| chr13:49063667 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11622A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063667 | |||||||
| chr13:49063668 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11621G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063668 | |||||||
| chr13:49063676 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11613A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063676 | |||||||
| chr13:49063677 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11612T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063677 | |||||||
| chr13:49063695 | CCTGGGCA others(14): Show |
C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11593_100-1157 others(25): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063695 | |||||||
| chr13:49063717 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11572G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063717 | |||||||
| chr13:49063719 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11570G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063719 | |||||||
| chr13:49063725 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11564A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063725 | |||||||
| chr13:49063736 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11553C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063736 | |||||||
| chr13:49063738 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11551C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063738 | |||||||
| chr13:49063739 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11550G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063739 | |||||||
| chr13:49063759 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11530T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063759 | |||||||
| chr13:49063761 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11528T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063761 | |||||||
| chr13:49063762 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11527T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063762 | |||||||
| chr13:49063776 | A | AGCTCTAA others(4): Show |
1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.100-11509_100-1150 others(15): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49063776 | ||||||
| chr13:49063836 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-11453T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063836 | |||||||
| chr13:49063837 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.100-11452A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063837 | |||||||
| chr13:49063881 | G | A | 1 | a0002c0003t0001g0002 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.100-11408G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49063881 | |||||||
| chr13:49064144 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.100-11145C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064144 | |||||||
| chr13:49064336 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0022 |
2 | NA18942.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.100-10953G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064336 | |||||||
| chr13:49064401 | G | GGC | 3 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0288 |
3 | HG02818.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.100-10888_100-1088 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064401 | |||||||
| chr13:49064401 | GC | G | 89 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(86): Show |
89 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.100-10878delC | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49064401 | ||||||
| chr13:49064411 | C | A | 6 | a0001c0001t0001g0100 a0001c0001t0001g0229 a0001c0001t0001g0287 others(3): Show |
6 | HG00733.hp2 HG02615.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-10878C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064411 | |||||||
| chr13:49064411 | C | CA | 84 | a0001c0001t0001g0052 a0001c0001t0001g0072 a0001c0001t0001g0135 others(81): Show |
84 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.100-10868dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49064411 | ||||||
| chr13:49064411 | C | CAA | 7 | a0001c0001t0001g0164 a0001c0001t0001g0168 a0001c0001t0001g0201 others(4): Show |
7 | HG01106.hp1 HG01496.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-10869_100-1086 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49064411 | ||||||
| chr13:49064411 | C | CCA | 34 | a0001c0001t0001g0162 a0001c0001t0001g0181 a0001c0001t0001g0184 others(31): Show |
34 | HG00438.hp1 HG00621.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-10878_100-1087 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064411 | |||||||
| chr13:49064412 | A | C | 5 | a0001c0001t0001g0092 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
5 | HG01257.hp1 HG03195.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-10877A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064412 | |||||||
| chr13:49064422 | C | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | NA18956.hp1 NA18968.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.100-10867C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064422 | |||||||
| chr13:49064426 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-10863A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064426 | |||||||
| chr13:49064607 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0208 |
2 | NA18948.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.100-10682G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064607 | |||||||
| chr13:49064650 | C | T | 1 | a0002c0003t0001g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-10639C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064650 | |||||||
| chr13:49064760 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(1): Show |
4 | HG02818.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-10529G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064760 | |||||||
| chr13:49064794 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100-10495A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064794 | |||||||
| chr13:49064810 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100-10479C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064810 | |||||||
| chr13:49064913 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.100-10376C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49064913 | |||||||
| chr13:49065013 | T | G | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.100-10276T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49065013 | |||||||
| chr13:49065058 | G | A | 1 | a0001c0002t0001g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.100-10231G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49065058 | |||||||
| chr13:49065249 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0030 others(136): Show |
139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.100-10040A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49065249 | |||||||
| chr13:49065322 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-9967A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49065322 | |||||||
| chr13:49065559 | A | G | 3 | a0001c0001t0001g0010 a0001c0005t0001g0155 a0001c0005t0001g0156 |
3 | HG00741.hp2 HG03017.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.100-9730A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49065559 | |||||||
| chr13:49065613 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.100-9676G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49065613 | |||||||
| chr13:49065937 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0059 |
3 | NA18956.hp2 NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.100-9352T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49065937 | |||||||
| chr13:49066056 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-9233A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49066056 | |||||||
| chr13:49066180 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-9109A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49066180 | |||||||
| chr13:49066307 | C | G | 1 | a0001c0001t0001g0292 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.100-8982C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49066307 | |||||||
| chr13:49066537 | C | G | 4 | a0003c0004t0001g0028 a0003c0004t0001g0031 a0003c0004t0001g0035 others(1): Show |
4 | HG00280.hp2 HG01515.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-8752C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49066537 | |||||||
| chr13:49066650 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-8639C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49066650 | |||||||
| chr13:49067001 | A | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-8288A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49067001 | |||||||
| chr13:49067002 | G | T | 2 | a0001c0001t0001g0124 a0005c0008t0001g0123 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.100-8287G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49067002 | |||||||
| chr13:49067282 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100-8007G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49067282 | |||||||
| chr13:49067393 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.100-7896G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49067393 | |||||||
| chr13:49067425 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.100-7864G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49067425 | |||||||
| chr13:49067577 | G | A | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.100-7712G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49067577 | |||||||
| chr13:49067673 | G | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0099 others(2): Show |
5 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-7616G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49067673 | |||||||
| chr13:49067679 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.100-7610G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49067679 | |||||||
| chr13:49067870 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.100-7419A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49067870 | |||||||
| chr13:49067961 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-7328C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49067961 | |||||||
| chr13:49068172 | T | TA | 6 | a0001c0001t0001g0092 a0001c0001t0001g0254 a0001c0001t0001g0255 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-7102dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49068172 | ||||||
| chr13:49068172 | TA | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0114 a0001c0001t0001g0118 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-7102delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49068172 | ||||||
| chr13:49068173 | A | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0192 |
2 | HG00609.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.100-7116A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49068173 | |||||||
| chr13:49068208 | G | GTGTT | 118 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(115): Show |
118 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.100-7078_100-7077i others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49068208 | ||||||
| chr13:49068268 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.100-7021A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49068268 | |||||||
| chr13:49068289 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-7000G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49068289 | |||||||
| chr13:49068371 | AAATT | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0077 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-6903_100-6900d others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49068371 | ||||||
| chr13:49068375 | T | A | 19 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0001g0168 others(16): Show |
19 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.100-6914T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49068375 | |||||||
| chr13:49068630 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-6659A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49068630 | |||||||
| chr13:49069170 | T | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.100-6119T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49069170 | |||||||
| chr13:49069387 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-5902A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49069387 | |||||||
| chr13:49069415 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.100-5874G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49069415 | |||||||
| chr13:49069617 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.100-5672A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49069617 | |||||||
| chr13:49069754 | T | C | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.100-5535T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49069754 | |||||||
| chr13:49069798 | G | A | 1 | a0002c0003t0001g0002 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.100-5491G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49069798 | |||||||
| chr13:49070005 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.100-5284A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070005 | |||||||
| chr13:49070083 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.100-5206T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070083 | |||||||
| chr13:49070272 | C | T | 1 | a0002c0003t0001g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-5017C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070272 | |||||||
| chr13:49070365 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.100-4924A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070365 | |||||||
| chr13:49070419 | A | G | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.100-4870A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070419 | |||||||
| chr13:49070666 | G | C | 1 | a0001c0001t0002g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.100-4623G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070666 | |||||||
| chr13:49070881 | C | CT | 230 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(227): Show |
230 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.100-4396dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49070881 | ||||||
| chr13:49070881 | C | CTT | 16 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(13): Show |
16 | HG00609.hp2 HG02040.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-4397_100-4396d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49070881 | ||||||
| chr13:49070893 | T | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.100-4396T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070893 | |||||||
| chr13:49070893 | TG | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01978.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-4395delG | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070893 | |||||||
| chr13:49070894 | G | T | 283 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(280): Show |
283 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.100-4395G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070894 | |||||||
| chr13:49070895 | T | G | 1 | a0001c0005t0001g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.100-4394T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070895 | |||||||
| chr13:49070896 | T | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.100-4393T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070896 | |||||||
| chr13:49070899 | G | T | 22 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0110 others(19): Show |
22 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.100-4390G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070899 | |||||||
| chr13:49070938 | G | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0213 |
2 | NA18947.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.100-4351G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49070938 | |||||||
| chr13:49071061 | C | CT | 121 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0160 others(118): Show |
121 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.100-4209dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49071061 | ||||||
| chr13:49071061 | C | CTT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0167 a0001c0001t0001g0188 others(6): Show |
9 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-4210_100-4209d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49071061 | ||||||
| chr13:49071061 | CT | C | 96 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
96 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.100-4209delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49071061 | ||||||
| chr13:49071244 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-4045A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49071244 | |||||||
| chr13:49071490 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(11): Show |
14 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-3799A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49071490 | |||||||
| chr13:49071567 | A | G | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG00639.hp1 HG01433.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3722A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49071567 | |||||||
| chr13:49071632 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.100-3657T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49071632 | |||||||
| chr13:49071633 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.100-3656G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49071633 | |||||||
| chr13:49071727 | G | GT | 138 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0077 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.100-3550dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49071727 | ||||||
| chr13:49071882 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.100-3407G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49071882 | |||||||
| chr13:49071894 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.100-3395C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49071894 | |||||||
| chr13:49072190 | G | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-3099G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49072190 | |||||||
| chr13:49072239 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-3050A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49072239 | |||||||
| chr13:49072242 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100-3047C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49072242 | |||||||
| chr13:49072361 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(11): Show |
14 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-2928A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49072361 | |||||||
| chr13:49072860 | T | TG | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.100-2427dupG | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49072860 | ||||||
| chr13:49073102 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-2187A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49073102 | |||||||
| chr13:49073436 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.100-1853G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49073436 | |||||||
| chr13:49073628 | T | C | 1 | a0001c0001t0001g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.100-1661T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49073628 | |||||||
| chr13:49073661 | G | GTA | 4 | a0001c0001t0001g0136 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | NA18973.hp2 NA18983.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1617_100-1616d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49073661 | ||||||
| chr13:49073694 | ATGTATAT others(12): Show |
A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.100-1574_100-1556d others(21): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49073694 | ||||||
| chr13:49073773 | A | ATATATAT others(29): Show |
3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.100-1499_100-1498i others(38): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49073773 | ||||||
| chr13:49073773 | A | ATATATAT others(111): Show |
1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-1499_100-1498i others(120): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49073773 | ||||||
| chr13:49073773 | A | ATATATAT others(29): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-1487_100-1452d others(38): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49073773 | ||||||
| chr13:49073773 | A | ATATATAT others(65): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.100-1452_100-1451i others(74): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49073773 | ||||||
| chr13:49073791 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.100-1498T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49073791 | |||||||
| chr13:49073860 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0105 |
2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.100-1429A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49073860 | |||||||
| chr13:49073869 | TATAC | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.100-1416_100-1413d others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49073869 | ||||||
| chr13:49074061 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-1228A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074061 | |||||||
| chr13:49074061 | A | T | 1 | a0001c0001t0001g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.100-1228A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074061 | |||||||
| chr13:49074217 | C | T | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.100-1072C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074217 | |||||||
| chr13:49074688 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-601A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074688 | |||||||
| chr13:49074717 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.100-572T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074717 | |||||||
| chr13:49074718 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.100-571A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074718 | |||||||
| chr13:49074810 | T | C | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.100-479T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074810 | |||||||
| chr13:49074889 | C | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.100-400C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074889 | |||||||
| chr13:49074925 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.100-364C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074925 | |||||||
| chr13:49074947 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-342T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074947 | |||||||
| chr13:49074989 | G | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-300G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49074989 | |||||||
| chr13:49075135 | A | AT | 21 | a0001c0001t0001g0125 a0001c0001t0001g0135 a0001c0001t0001g0136 others(18): Show |
21 | HG01257.hp1 HG02257.hp1 HG02896.hp2 others(18): Show |
intron_variant | MODIFIER | c.100-146dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr13 | 49075135 | ||||||
| chr13:49075275 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.100-14C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49075275 | |||||||
| chr13:49075281 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG01070.hp2 | splice_region_variant&intron_variant | LOW | c.100-8T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 2/25 | chr13 | 49075281 | |||||||
| chr13:49075393 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.175+29T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49075393 | |||||||
| chr13:49075510 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.175+146G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49075510 | |||||||
| chr13:49075520 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.175+156G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49075520 | |||||||
| chr13:49075800 | G | GC | 234 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(231): Show |
234 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.175+444dupC | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49075800 | ||||||
| chr13:49075800 | G | GCC | 40 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(37): Show |
40 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.175+443_175+444dup others(2): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49075800 | ||||||
| chr13:49075809 | A | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0067 a0001c0001t0001g0252 others(3): Show |
6 | HG01978.hp1 HG02523.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+445A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49075809 | |||||||
| chr13:49075882 | T | G | 1 | a0001c0001t0010g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.175+518T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49075882 | |||||||
| chr13:49076040 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.175+676T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49076040 | |||||||
| chr13:49076228 | A | G | 11 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | NA18948.hp2 NA18967.hp1 NA18973.hp2 others(8): Show |
intron_variant | MODIFIER | c.175+864A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49076228 | |||||||
| chr13:49076464 | T | C | 9 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(6): Show |
9 | HG00733.hp1 HG01516.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+1100T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49076464 | |||||||
| chr13:49076633 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.175+1269C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49076633 | |||||||
| chr13:49076761 | A | C | 1 | a0006c0006t0001g0074 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.175+1397A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49076761 | |||||||
| chr13:49076826 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.175+1462T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49076826 | |||||||
| chr13:49076894 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.175+1530G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49076894 | |||||||
| chr13:49076913 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.175+1549C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49076913 | |||||||
| chr13:49076917 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.175+1553T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49076917 | |||||||
| chr13:49077012 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.175+1648T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077012 | |||||||
| chr13:49077159 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.175+1795A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077159 | |||||||
| chr13:49077208 | G | A | 7 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
7 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+1844G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077208 | |||||||
| chr13:49077212 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.175+1848G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077212 | |||||||
| chr13:49077635 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.175+2271C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077635 | |||||||
| chr13:49077644 | G | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.175+2280G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077644 | |||||||
| chr13:49077782 | A | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.175+2418A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077782 | |||||||
| chr13:49077796 | T | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.175+2432T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077796 | |||||||
| chr13:49077801 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175+2437T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077801 | |||||||
| chr13:49077862 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.175+2498G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077862 | |||||||
| chr13:49077874 | A | G | 1 | a0001c0001t0006g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.175+2510A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49077874 | |||||||
| chr13:49078218 | A | G | 14 | a0001c0001t0001g0115 a0001c0002t0001g0009 a0001c0002t0001g0086 others(11): Show |
14 | HG01496.hp2 HG02055.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.175+2854A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49078218 | |||||||
| chr13:49078228 | T | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.175+2864T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49078228 | |||||||
| chr13:49078238 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.175+2874A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49078238 | |||||||
| chr13:49078285 | G | A | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.175+2921G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49078285 | |||||||
| chr13:49078304 | A | G | 1 | a0001c0001t0006g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.175+2940A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49078304 | |||||||
| chr13:49078317 | CCTAT | C | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.175+2957_175+2960d others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49078317 | ||||||
| chr13:49078382 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.175+3018A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49078382 | |||||||
| chr13:49078716 | C | T | 1 | a0003c0004t0001g0045 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.175+3352C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49078716 | |||||||
| chr13:49078863 | G | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+3499G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49078863 | |||||||
| chr13:49078964 | T | G | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.175+3600T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49078964 | |||||||
| chr13:49079087 | G | A | 2 | a0001c0001t0003g0183 a0001c0001t0003g0196 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.175+3723G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49079087 | |||||||
| chr13:49079258 | G | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.175+3894G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49079258 | |||||||
| chr13:49079279 | A | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0022 |
2 | NA18942.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.175+3915A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49079279 | |||||||
| chr13:49079552 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+4188A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49079552 | |||||||
| chr13:49079717 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.175+4353C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49079717 | |||||||
| chr13:49079729 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0006g0161 |
3 | HG02145.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.175+4365C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49079729 | |||||||
| chr13:49079753 | G | GA | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+4397dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49079753 | ||||||
| chr13:49080104 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.175+4740T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49080104 | |||||||
| chr13:49080303 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.175+4939G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49080303 | |||||||
| chr13:49080396 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+5032C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49080396 | |||||||
| chr13:49080415 | G | A | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.175+5051G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49080415 | |||||||
| chr13:49080520 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.175+5156G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49080520 | |||||||
| chr13:49080874 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.175+5510G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49080874 | |||||||
| chr13:49081016 | C | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.175+5652C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49081016 | |||||||
| chr13:49081157 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.175+5793C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49081157 | |||||||
| chr13:49081203 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.175+5839A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49081203 | |||||||
| chr13:49081434 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175+6070G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49081434 | |||||||
| chr13:49081593 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.175+6229G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49081593 | |||||||
| chr13:49081604 | T | C | 1 | a0001c0002t0001g0117 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.175+6240T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49081604 | |||||||
| chr13:49081968 | CT | C | 278 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(275): Show |
278 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.175+6619delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49081968 | ||||||
| chr13:49081992 | TAAA | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+6631_175+6633d others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49081992 | ||||||
| chr13:49082161 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.175+6797G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49082161 | |||||||
| chr13:49082279 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.175+6915G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49082279 | |||||||
| chr13:49082375 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.175+7011G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49082375 | |||||||
| chr13:49082391 | CAAAA | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(1): Show |
4 | HG02818.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+7031_175+7034d others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49082391 | ||||||
| chr13:49082405 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+7041A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49082405 | |||||||
| chr13:49082442 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.175+7078G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49082442 | |||||||
| chr13:49083187 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.175+7823C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083187 | |||||||
| chr13:49083217 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.175+7853G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083217 | |||||||
| chr13:49083371 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.175+8007C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083371 | |||||||
| chr13:49083446 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175+8082T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083446 | |||||||
| chr13:49083484 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.175+8120C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083484 | |||||||
| chr13:49083500 | T | G | 114 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(111): Show |
114 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.175+8136T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083500 | |||||||
| chr13:49083631 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.175+8267T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083631 | |||||||
| chr13:49083663 | C | T | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.175+8299C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083663 | |||||||
| chr13:49083691 | G | C | 24 | a0001c0001t0001g0012 a0001c0001t0001g0075 a0001c0001t0001g0076 others(21): Show |
24 | HG00639.hp1 HG00733.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.175+8327G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083691 | |||||||
| chr13:49083741 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.175+8377A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083741 | |||||||
| chr13:49083754 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.175+8390G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083754 | |||||||
| chr13:49083837 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.175+8473T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49083837 | |||||||
| chr13:49084073 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.175+8709A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49084073 | |||||||
| chr13:49085157 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.175+9793G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49085157 | |||||||
| chr13:49085168 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.175+9804G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49085168 | |||||||
| chr13:49085169 | C | CT | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.175+9810dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49085169 | ||||||
| chr13:49085287 | G | C | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.175+9923G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49085287 | |||||||
| chr13:49085423 | GGA | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+10065_175+1006 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49085423 | ||||||
| chr13:49085446 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.175+10082A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49085446 | |||||||
| chr13:49085875 | CCTT | C | 4 | a0001c0001t0001g0186 a0001c0001t0001g0224 a0001c0001t0003g0183 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+10512_175+1051 others(7): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49085875 | |||||||
| chr13:49085876 | C | CT | 21 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0071 others(18): Show |
21 | HG00741.hp2 HG01243.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.175+10530dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49085876 | ||||||
| chr13:49085876 | CT | C | 7 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
7 | HG01074.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+10530delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49085876 | ||||||
| chr13:49085876 | CTT | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+10529_175+1053 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49085876 | ||||||
| chr13:49085968 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.175+10604T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49085968 | |||||||
| chr13:49085971 | C | T | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG01891.hp1 HG02698.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+10607C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49085971 | |||||||
| chr13:49086141 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.175+10777T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49086141 | |||||||
| chr13:49086271 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.175+10907G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49086271 | |||||||
| chr13:49086282 | A | G | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+10918A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49086282 | |||||||
| chr13:49086491 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.175+11127G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49086491 | |||||||
| chr13:49086602 | T | G | 1 | a0001c0001t0001g0279 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.175+11238T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49086602 | |||||||
| chr13:49086868 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.175+11504A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49086868 | |||||||
| chr13:49087693 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.175+12329A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49087693 | |||||||
| chr13:49087861 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.175+12497A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49087861 | |||||||
| chr13:49087922 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.175+12558A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49087922 | |||||||
| chr13:49088395 | C | G | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.175+13031C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49088395 | |||||||
| chr13:49088430 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.175+13066A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49088430 | |||||||
| chr13:49088511 | T | G | 1 | a0001c0001t0001g0289 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.175+13147T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49088511 | |||||||
| chr13:49088673 | G | A | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.175+13309G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49088673 | |||||||
| chr13:49088772 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0006g0161 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.175+13408C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49088772 | |||||||
| chr13:49088791 | G | A | 5 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+13427G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49088791 | |||||||
| chr13:49088926 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.175+13562A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49088926 | |||||||
| chr13:49088936 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.175+13572A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49088936 | |||||||
| chr13:49088987 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.175+13623A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49088987 | |||||||
| chr13:49089095 | A | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0077 others(9): Show |
12 | HG01243.hp1 HG02258.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+13731A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49089095 | |||||||
| chr13:49089304 | A | G | 16 | a0001c0001t0001g0168 a0001c0001t0001g0245 a0001c0001t0001g0247 others(13): Show |
16 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.175+13940A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49089304 | |||||||
| chr13:49089544 | G | C | 1 | a0001c0002t0001g0117 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.175+14180G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49089544 | |||||||
| chr13:49089616 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0059 |
3 | NA18956.hp2 NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.175+14252T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49089616 | |||||||
| chr13:49089779 | G | A | 107 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(104): Show |
107 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.175+14415G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49089779 | |||||||
| chr13:49090273 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.175+14909T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49090273 | |||||||
| chr13:49090356 | G | T | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.175+14992G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49090356 | |||||||
| chr13:49090373 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.175+15009C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49090373 | |||||||
| chr13:49090408 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.175+15044C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49090408 | |||||||
| chr13:49090570 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.175+15206C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49090570 | |||||||
| chr13:49090701 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.175+15337T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49090701 | |||||||
| chr13:49090751 | C | T | 1 | a0001c0005t0001g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.175+15387C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49090751 | |||||||
| chr13:49090830 | A | C | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG01891.hp1 HG02698.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+15466A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49090830 | |||||||
| chr13:49090929 | G | C | 1 | a0001c0002t0001g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.175+15565G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49090929 | |||||||
| chr13:49091451 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.175+16087T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49091451 | |||||||
| chr13:49091504 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.175+16140C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49091504 | |||||||
| chr13:49091723 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.175+16359G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49091723 | |||||||
| chr13:49091744 | G | A | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.175+16380G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49091744 | |||||||
| chr13:49091913 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175+16549G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49091913 | |||||||
| chr13:49091964 | C | T | 1 | a0001c0002t0001g0113 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.175+16600C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49091964 | |||||||
| chr13:49091987 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.175+16623A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49091987 | |||||||
| chr13:49092022 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.175+16658G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49092022 | |||||||
| chr13:49092026 | G | T | 1 | a0001c0001t0001g0208 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.175+16662G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49092026 | |||||||
| chr13:49092139 | T | C | 13 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(10): Show |
13 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+16775T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49092139 | |||||||
| chr13:49092363 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.175+16999A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49092363 | |||||||
| chr13:49092449 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(149): Show |
152 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.175+17085T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49092449 | |||||||
| chr13:49092760 | T | TA | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+17410dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49092760 | ||||||
| chr13:49092880 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.175+17516A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49092880 | |||||||
| chr13:49092891 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+17527A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49092891 | |||||||
| chr13:49092966 | TAA | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.175+17603_175+1760 others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49092966 | |||||||
| chr13:49093068 | T | A | 1 | a0001c0001t0002g0177 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.175+17704T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49093068 | |||||||
| chr13:49093312 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.175+17948A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49093312 | |||||||
| chr13:49093543 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+18179C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49093543 | |||||||
| chr13:49093716 | C | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.175+18352C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49093716 | |||||||
| chr13:49093793 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.175+18429A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49093793 | |||||||
| chr13:49093829 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.175+18465A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49093829 | |||||||
| chr13:49094226 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.175+18862G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49094226 | |||||||
| chr13:49094227 | TTAA | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.175+18867_175+1886 others(7): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49094227 | ||||||
| chr13:49094334 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+18970T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49094334 | |||||||
| chr13:49094538 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18943.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.175+19174T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49094538 | |||||||
| chr13:49094753 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.175+19389A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49094753 | |||||||
| chr13:49095121 | A | G | 5 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0274 others(2): Show |
5 | HG01071.hp1 HG02109.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-19534A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49095121 | |||||||
| chr13:49095131 | A | T | 1 | a0002c0003t0001g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.176-19524A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49095131 | |||||||
| chr13:49095137 | G | A | 2 | a0001c0001t0001g0192 a0004c0007t0001g0191 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.176-19518G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49095137 | |||||||
| chr13:49095147 | T | A | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.176-19508T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49095147 | |||||||
| chr13:49095376 | G | A | 1 | a0003c0004t0001g0028 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.176-19279G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49095376 | |||||||
| chr13:49095675 | A | C | 4 | a0001c0001t0001g0136 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | NA18973.hp2 NA18983.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-18980A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49095675 | |||||||
| chr13:49095766 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.176-18889G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49095766 | |||||||
| chr13:49095984 | C | T | 4 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0246 others(1): Show |
4 | NA18953.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-18671C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49095984 | |||||||
| chr13:49096045 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.176-18610T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096045 | |||||||
| chr13:49096085 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.176-18570C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096085 | |||||||
| chr13:49096116 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.176-18539A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096116 | |||||||
| chr13:49096256 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.176-18399A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096256 | |||||||
| chr13:49096383 | A | C | 1 | a0003c0004t0001g0045 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.176-18272A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096383 | |||||||
| chr13:49096450 | T | G | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.176-18205T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096450 | |||||||
| chr13:49096460 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.176-18195C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096460 | |||||||
| chr13:49096581 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.176-18074T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096581 | |||||||
| chr13:49096684 | G | A | 128 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(125): Show |
128 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.176-17971G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096684 | |||||||
| chr13:49096819 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.176-17836G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096819 | |||||||
| chr13:49096917 | G | A | 6 | a0001c0001t0001g0065 a0003c0004t0001g0028 a0003c0004t0001g0031 others(3): Show |
6 | HG00280.hp2 HG01515.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-17738G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49096917 | |||||||
| chr13:49097079 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(149): Show |
152 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.176-17576G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49097079 | |||||||
| chr13:49097147 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-17508C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49097147 | |||||||
| chr13:49097372 | T | A | 48 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(45): Show |
48 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.176-17283T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49097372 | |||||||
| chr13:49097723 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0099 others(2): Show |
5 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.176-16932G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49097723 | |||||||
| chr13:49098043 | A | G | 4 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0262 others(1): Show |
4 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-16612A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49098043 | |||||||
| chr13:49098205 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-16450C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49098205 | |||||||
| chr13:49098304 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.176-16351G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49098304 | |||||||
| chr13:49098405 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.176-16250C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49098405 | |||||||
| chr13:49098628 | A | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.176-16027A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49098628 | |||||||
| chr13:49099087 | A | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0001g0285 |
3 | HG02109.hp2 HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.176-15568A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49099087 | |||||||
| chr13:49099322 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-15333C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49099322 | |||||||
| chr13:49099467 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.176-15188G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49099467 | |||||||
| chr13:49099713 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.176-14942C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49099713 | |||||||
| chr13:49099734 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.176-14921A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49099734 | |||||||
| chr13:49099778 | A | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-14877A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49099778 | |||||||
| chr13:49099796 | A | C | 2 | a0001c0001t0001g0025 a0001c0001t0008g0051 |
2 | NA18939.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.176-14859A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49099796 | |||||||
| chr13:49100111 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.176-14544A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49100111 | |||||||
| chr13:49100154 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.176-14501C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49100154 | |||||||
| chr13:49100197 | G | A | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.176-14458G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49100197 | |||||||
| chr13:49100205 | T | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.176-14450T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49100205 | |||||||
| chr13:49100525 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.176-14130G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49100525 | |||||||
| chr13:49100688 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.176-13967G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49100688 | |||||||
| chr13:49100793 | A | T | 13 | a0001c0002t0001g0009 a0001c0002t0001g0086 a0001c0002t0001g0087 others(10): Show |
13 | HG01496.hp2 HG02055.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.176-13862A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49100793 | |||||||
| chr13:49101049 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.176-13606G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49101049 | |||||||
| chr13:49101060 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.176-13595T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49101060 | |||||||
| chr13:49101106 | A | C | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG01891.hp1 HG02698.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-13549A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49101106 | |||||||
| chr13:49101168 | C | G | 1 | a0001c0001t0002g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.176-13487C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49101168 | |||||||
| chr13:49101428 | A | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-13227A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49101428 | |||||||
| chr13:49101562 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(142): Show |
145 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.176-13093C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49101562 | |||||||
| chr13:49101794 | G | GT | 25 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0044 others(22): Show |
25 | HG00438.hp1 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.176-12839dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49101794 | ||||||
| chr13:49101794 | GT | G | 15 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0046 others(12): Show |
15 | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.176-12839delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49101794 | ||||||
| chr13:49101804 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.176-12851T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49101804 | |||||||
| chr13:49101975 | C | G | 1 | a0001c0001t0001g0039 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.176-12680C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49101975 | |||||||
| chr13:49102028 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.176-12627T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49102028 | |||||||
| chr13:49102049 | G | C | 1 | a0001c0001t0001g0027 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.176-12606G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49102049 | |||||||
| chr13:49102080 | C | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.176-12575C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49102080 | |||||||
| chr13:49102129 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.176-12526G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49102129 | |||||||
| chr13:49102134 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.176-12521T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49102134 | |||||||
| chr13:49102287 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.176-12368G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49102287 | |||||||
| chr13:49102557 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.176-12098T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49102557 | |||||||
| chr13:49102596 | C | T | 16 | a0001c0001t0001g0168 a0001c0001t0001g0245 a0001c0001t0001g0247 others(13): Show |
16 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.176-12059C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49102596 | |||||||
| chr13:49102671 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.176-11984G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49102671 | |||||||
| chr13:49103471 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.176-11184A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49103471 | |||||||
| chr13:49103885 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.176-10770A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49103885 | |||||||
| chr13:49104063 | T | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.176-10592T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49104063 | |||||||
| chr13:49104091 | T | C | 1 | a0001c0001t0002g0175 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.176-10564T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49104091 | |||||||
| chr13:49104228 | T | C | 2 | a0001c0001t0002g0173 a0001c0001t0002g0174 |
2 | HG00621.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.176-10427T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49104228 | |||||||
| chr13:49104299 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.176-10356G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49104299 | |||||||
| chr13:49104451 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.176-10204G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49104451 | |||||||
| chr13:49104452 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.176-10203A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49104452 | |||||||
| chr13:49104481 | G | A | 14 | a0001c0001t0001g0185 a0001c0001t0001g0190 a0001c0001t0001g0195 others(11): Show |
14 | HG01433.hp2 HG01928.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.176-10174G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49104481 | |||||||
| chr13:49104805 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.176-9850C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49104805 | |||||||
| chr13:49104871 | A | G | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0234 |
3 | NA18944.hp1 NA18962.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.176-9784A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49104871 | |||||||
| chr13:49104885 | G | A | 127 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.176-9770G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49104885 | |||||||
| chr13:49105002 | C | T | 6 | a0001c0001t0001g0065 a0003c0004t0001g0028 a0003c0004t0001g0031 others(3): Show |
6 | HG00280.hp2 HG01515.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-9653C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49105002 | |||||||
| chr13:49105021 | A | G | 31 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0075 others(28): Show |
31 | HG00639.hp1 HG00733.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.176-9634A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49105021 | |||||||
| chr13:49105039 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.176-9616C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49105039 | |||||||
| chr13:49105453 | A | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.176-9202A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49105453 | |||||||
| chr13:49105526 | A | T | 1 | a0005c0008t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.176-9129A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49105526 | |||||||
| chr13:49105648 | C | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.176-9007C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49105648 | |||||||
| chr13:49106592 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.176-8063C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49106592 | |||||||
| chr13:49106773 | C | CA | 227 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(224): Show |
227 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.176-7862dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49106773 | ||||||
| chr13:49106773 | C | CAA | 21 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0046 others(18): Show |
21 | HG00741.hp1 HG01070.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.176-7863_176-7862d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49106773 | ||||||
| chr13:49107008 | A | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18943.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.176-7647A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49107008 | |||||||
| chr13:49107088 | C | G | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.176-7567C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49107088 | |||||||
| chr13:49107205 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.176-7450G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49107205 | |||||||
| chr13:49107219 | TAG | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.176-7433_176-7432d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49107219 | ||||||
| chr13:49107276 | TAG | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG02135.hp1 NA18956.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-7376_176-7375d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49107276 | ||||||
| chr13:49107486 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.176-7169C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49107486 | |||||||
| chr13:49107574 | GCTT | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.176-7075_176-7073d others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49107574 | ||||||
| chr13:49107583 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
13 | HG01167.hp2 HG01175.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.176-7072G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49107583 | |||||||
| chr13:49107920 | A | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.176-6735A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49107920 | |||||||
| chr13:49108523 | C | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(1): Show |
4 | HG02818.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-6132C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49108523 | |||||||
| chr13:49108744 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0131 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.176-5911A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49108744 | |||||||
| chr13:49108746 | G | T | 1 | a0001c0001t0001g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.176-5909G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49108746 | |||||||
| chr13:49108858 | C | G | 1 | a0001c0001t0001g0040 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.176-5797C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49108858 | |||||||
| chr13:49109107 | A | C | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.176-5548A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49109107 | |||||||
| chr13:49109116 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.176-5539C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49109116 | |||||||
| chr13:49109404 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(11): Show |
14 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.176-5251A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49109404 | |||||||
| chr13:49109553 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.176-5102A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49109553 | |||||||
| chr13:49109584 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.176-5071C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49109584 | |||||||
| chr13:49109792 | A | T | 1 | a0001c0001t0001g0289 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.176-4863A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49109792 | |||||||
| chr13:49109916 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.176-4739A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49109916 | |||||||
| chr13:49110205 | C | CT | 119 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0126 others(116): Show |
119 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.176-4442dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49110205 | ||||||
| chr13:49110214 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.176-4441C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49110214 | |||||||
| chr13:49110300 | C | CA | 9 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0083 others(6): Show |
9 | HG01243.hp1 HG01928.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-4342dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49110300 | ||||||
| chr13:49110686 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0021 |
2 | NA18959.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.176-3969G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49110686 | |||||||
| chr13:49110688 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.176-3967G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49110688 | |||||||
| chr13:49110893 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.176-3762G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49110893 | |||||||
| chr13:49110964 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.176-3691G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49110964 | |||||||
| chr13:49110992 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.176-3663G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49110992 | |||||||
| chr13:49111037 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.176-3618A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111037 | |||||||
| chr13:49111043 | T | G | 1 | a0001c0001t0001g0205 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.176-3612T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111043 | |||||||
| chr13:49111259 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.176-3396G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111259 | |||||||
| chr13:49111305 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.176-3350G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111305 | |||||||
| chr13:49111340 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.176-3315T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111340 | |||||||
| chr13:49111401 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.176-3254A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111401 | |||||||
| chr13:49111540 | A | G | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.176-3115A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111540 | |||||||
| chr13:49111578 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.176-3077T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111578 | |||||||
| chr13:49111612 | G | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.176-3043G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111612 | |||||||
| chr13:49111682 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0243 |
2 | NA18959.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.176-2973C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111682 | |||||||
| chr13:49111725 | C | CA | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0048 others(20): Show |
23 | HG01243.hp1 HG01258.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.176-2912dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49111725 | ||||||
| chr13:49111753 | G | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(138): Show |
141 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.176-2902G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111753 | |||||||
| chr13:49111764 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.176-2891G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111764 | |||||||
| chr13:49111783 | A | T | 26 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0025 others(23): Show |
26 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.176-2872A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111783 | |||||||
| chr13:49111784 | T | A | 17 | a0001c0001t0001g0154 a0001c0001t0001g0168 a0001c0001t0001g0245 others(14): Show |
17 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.176-2871T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111784 | |||||||
| chr13:49111896 | C | G | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.176-2759C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111896 | |||||||
| chr13:49111972 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.176-2683G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49111972 | |||||||
| chr13:49112010 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(139): Show |
142 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.176-2645T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49112010 | |||||||
| chr13:49113106 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.176-1549A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49113106 | |||||||
| chr13:49113319 | C | CT | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.176-1336_176-1335i others(3): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49113319 | |||||||
| chr13:49113471 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.176-1184G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49113471 | |||||||
| chr13:49113485 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.176-1170C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49113485 | |||||||
| chr13:49113602 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.176-1053A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49113602 | |||||||
| chr13:49113699 | C | G | 1 | a0001c0001t0001g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.176-956C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49113699 | |||||||
| chr13:49114033 | T | A | 7 | a0001c0001t0001g0192 a0002c0003t0001g0002 a0002c0003t0001g0003 others(4): Show |
7 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-622T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49114033 | |||||||
| chr13:49114410 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.176-245T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49114410 | |||||||
| chr13:49114410 | T | TC | 34 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0030 others(31): Show |
34 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.176-241dupC | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr13 | 49114410 | ||||||
| chr13:49114414 | CG | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0053 a0001c0001t0001g0124 others(67): Show |
70 | HG00280.hp1 HG00597.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.176-240delG | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49114414 | |||||||
| chr13:49114415 | G | C | 219 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
219 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.176-240G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49114415 | |||||||
| chr13:49114416 | C | G | 1 | a0002c0003t0001g0002 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.176-239C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49114416 | |||||||
| chr13:49114419 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.176-236C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49114419 | |||||||
| chr13:49114419 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.176-236C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49114419 | |||||||
| chr13:49114419 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0125 |
2 | HG01257.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.176-236C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49114419 | |||||||
| chr13:49114420 | C | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | NA18612.hp2 NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.176-235C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49114420 | |||||||
| chr13:49114422 | A | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0235 |
2 | HG02109.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.176-233A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 3/25 | chr13 | 49114422 | |||||||
| chr13:49115076 | C | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.252+345C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115076 | |||||||
| chr13:49115120 | A | G | 8 | a0001c0001t0001g0075 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG00639.hp1 HG00733.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+389A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115120 | |||||||
| chr13:49115183 | AGG | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0075 a0001c0001t0001g0076 others(22): Show |
25 | HG00639.hp1 HG01243.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.252+462_252+463del others(2): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr13 | 49115183 | ||||||
| chr13:49115185 | G | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.252+454G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115185 | |||||||
| chr13:49115186 | G | T | 9 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0171 others(6): Show |
9 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+455G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115186 | |||||||
| chr13:49115188 | G | T | 1 | a0001c0001t0002g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.252+457G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115188 | |||||||
| chr13:49115191 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.252+460G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115191 | |||||||
| chr13:49115193 | G | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG02717.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+462G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115193 | |||||||
| chr13:49115194 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(204): Show |
207 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.252+463G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115194 | |||||||
| chr13:49115194 | GA | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.252+466delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr13 | 49115194 | ||||||
| chr13:49115195 | A | AAT | 12 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0167 others(9): Show |
12 | HG02698.hp1 HG02738.hp1 HG03688.hp2 others(9): Show |
intron_variant | MODIFIER | c.252+465_252+466ins others(2): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr13 | 49115195 | ||||||
| chr13:49115195 | A | G | 2 | a0001c0001t0001g0127 a0001c0005t0001g0156 |
2 | HG00741.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.252+464A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115195 | |||||||
| chr13:49115196 | A | AT | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0029 others(33): Show |
36 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.252+465_252+466ins others(1): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115196 | |||||||
| chr13:49115196 | A | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0130 |
2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.252+465A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115196 | |||||||
| chr13:49115197 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(155): Show |
158 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.252+466A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115197 | |||||||
| chr13:49115198 | T | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(207): Show |
210 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.252+467T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115198 | |||||||
| chr13:49115198 | T | TA | 51 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(48): Show |
51 | HG00597.hp2 HG00639.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.252+479dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr13 | 49115198 | ||||||
| chr13:49115198 | T | TAA | 7 | a0001c0001t0001g0136 a0001c0001t0001g0140 a0001c0001t0001g0142 others(4): Show |
7 | HG00733.hp2 NA18948.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+478_252+479dup others(2): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr13 | 49115198 | ||||||
| chr13:49115541 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.252+810C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49115541 | |||||||
| chr13:49116024 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.252+1293A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116024 | |||||||
| chr13:49116255 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1524C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116255 | |||||||
| chr13:49116418 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.252+1687T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116418 | |||||||
| chr13:49116423 | A | C | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.252+1692A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116423 | |||||||
| chr13:49116442 | A | T | 1 | a0001c0001t0001g0269 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.252+1711A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116442 | |||||||
| chr13:49116522 | T | G | 1 | a0001c0001t0001g0233 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.252+1791T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116522 | |||||||
| chr13:49116524 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.252+1793G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116524 | |||||||
| chr13:49116524 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.252+1793G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116524 | |||||||
| chr13:49116525 | T | G | 1 | a0001c0001t0001g0233 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.252+1794T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116525 | |||||||
| chr13:49116726 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.252+1995C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116726 | |||||||
| chr13:49116772 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252+2041T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116772 | |||||||
| chr13:49116780 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.252+2049C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49116780 | |||||||
| chr13:49116785 | C | CA | 217 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.252+2069dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr13 | 49116785 | ||||||
| chr13:49116785 | C | CAA | 34 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0064 others(31): Show |
34 | HG01243.hp1 HG01243.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.252+2068_252+2069d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr13 | 49116785 | ||||||
| chr13:49117032 | A | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.252+2301A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49117032 | |||||||
| chr13:49117054 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.252+2323G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49117054 | |||||||
| chr13:49117088 | C | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.252+2357C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49117088 | |||||||
| chr13:49117088 | CA | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0242 |
3 | HG02630.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.252+2358delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49117088 | |||||||
| chr13:49117119 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.252+2388A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49117119 | |||||||
| chr13:49117255 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.252+2524T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49117255 | |||||||
| chr13:49117858 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252+3127A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49117858 | |||||||
| chr13:49118036 | G | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+3305G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49118036 | |||||||
| chr13:49118281 | A | T | 1 | a0001c0002t0001g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.252+3550A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49118281 | |||||||
| chr13:49118345 | A | G | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.252+3614A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49118345 | |||||||
| chr13:49118415 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.252+3684C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49118415 | |||||||
| chr13:49118659 | G | C | 1 | a0003c0004t0001g0045 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.252+3928G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49118659 | |||||||
| chr13:49118764 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.252+4033C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49118764 | |||||||
| chr13:49118801 | C | G | 6 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
6 | HG01433.hp2 HG01934.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+4070C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49118801 | |||||||
| chr13:49118916 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+4185G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49118916 | |||||||
| chr13:49118923 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.252+4192C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49118923 | |||||||
| chr13:49119096 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.252+4365A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119096 | |||||||
| chr13:49119114 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.252+4383G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119114 | |||||||
| chr13:49119115 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.252+4384C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119115 | |||||||
| chr13:49119137 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.252+4406G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119137 | |||||||
| chr13:49119178 | G | C | 1 | a0001c0001t0001g0070 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.252+4447G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119178 | |||||||
| chr13:49119187 | C | A | 1 | a0001c0001t0001g0039 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.252+4456C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119187 | |||||||
| chr13:49119362 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.252+4631G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119362 | |||||||
| chr13:49119380 | C | A | 1 | a0001c0001t0001g0039 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.252+4649C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119380 | |||||||
| chr13:49119381 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+4650A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119381 | |||||||
| chr13:49119493 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.252+4762C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119493 | |||||||
| chr13:49119784 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.252+5053T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119784 | |||||||
| chr13:49119839 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0048 |
2 | NA18947.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.252+5108G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49119839 | |||||||
| chr13:49120055 | G | A | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.252+5324G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49120055 | |||||||
| chr13:49120227 | A | C | 1 | a0001c0001t0001g0230 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.252+5496A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49120227 | |||||||
| chr13:49120451 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG00438.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.252+5720G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49120451 | |||||||
| chr13:49120474 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.252+5743G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49120474 | |||||||
| chr13:49121064 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.252+6333G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49121064 | |||||||
| chr13:49121083 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.252+6352A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49121083 | |||||||
| chr13:49121175 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.252+6444C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49121175 | |||||||
| chr13:49121322 | A | C | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.252+6591A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49121322 | |||||||
| chr13:49121594 | C | T | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG01891.hp1 HG02698.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+6863C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49121594 | |||||||
| chr13:49121731 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.252+7000T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49121731 | |||||||
| chr13:49121976 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.252+7245G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49121976 | |||||||
| chr13:49122037 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.252+7306G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49122037 | |||||||
| chr13:49122103 | A | C | 120 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
120 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.252+7372A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49122103 | |||||||
| chr13:49122385 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.252+7654C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49122385 | |||||||
| chr13:49122539 | G | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+7808G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49122539 | |||||||
| chr13:49122721 | C | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0240 a0001c0001t0006g0161 |
3 | HG02145.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.252+7990C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49122721 | |||||||
| chr13:49122746 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.252+8015A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49122746 | |||||||
| chr13:49122924 | C | G | 1 | a0001c0002t0001g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.252+8193C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49122924 | |||||||
| chr13:49122947 | C | T | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-8190C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49122947 | |||||||
| chr13:49123064 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.253-8073G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49123064 | |||||||
| chr13:49123367 | A | C | 120 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
120 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.253-7770A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49123367 | |||||||
| chr13:49123600 | A | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0077 others(9): Show |
12 | HG01243.hp1 HG02258.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.253-7537A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49123600 | |||||||
| chr13:49123662 | A | C | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.253-7475A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49123662 | |||||||
| chr13:49123721 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.253-7416T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49123721 | |||||||
| chr13:49124112 | C | G | 124 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(121): Show |
124 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.253-7025C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49124112 | |||||||
| chr13:49124142 | C | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0056 others(12): Show |
15 | HG00544.hp1 HG02074.hp2 HG03927.hp1 others(12): Show |
intron_variant | MODIFIER | c.253-6995C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49124142 | |||||||
| chr13:49124355 | A | T | 1 | a0001c0001t0001g0021 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.253-6782A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49124355 | |||||||
| chr13:49124397 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.253-6740G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49124397 | |||||||
| chr13:49124501 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.253-6636G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49124501 | |||||||
| chr13:49124535 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.253-6602A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49124535 | |||||||
| chr13:49124698 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.253-6439G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49124698 | |||||||
| chr13:49124913 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.253-6224T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49124913 | |||||||
| chr13:49125143 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.253-5994A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125143 | |||||||
| chr13:49125210 | T | A | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.253-5927T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125210 | |||||||
| chr13:49125211 | G | A | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.253-5926G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125211 | |||||||
| chr13:49125217 | A | T | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.253-5920A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125217 | |||||||
| chr13:49125222 | T | C | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.253-5915T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125222 | |||||||
| chr13:49125223 | C | T | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.253-5914C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125223 | |||||||
| chr13:49125224 | T | C | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.253-5913T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125224 | |||||||
| chr13:49125225 | T | A | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.253-5912T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125225 | |||||||
| chr13:49125256 | G | A | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.253-5881G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125256 | |||||||
| chr13:49125502 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.253-5635A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125502 | |||||||
| chr13:49125653 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.253-5484T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125653 | |||||||
| chr13:49125834 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.253-5303A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125834 | |||||||
| chr13:49125929 | A | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.253-5208A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49125929 | |||||||
| chr13:49126001 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.253-5136T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49126001 | |||||||
| chr13:49126198 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(147): Show |
150 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.253-4939G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49126198 | |||||||
| chr13:49126269 | T | G | 118 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(115): Show |
118 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.253-4868T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49126269 | |||||||
| chr13:49126274 | GTTT | G | 59 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(56): Show |
59 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.253-4858_253-4856d others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr13 | 49126274 | ||||||
| chr13:49126399 | G | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.253-4738G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49126399 | |||||||
| chr13:49126881 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.253-4256T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49126881 | |||||||
| chr13:49127022 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.253-4115T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49127022 | |||||||
| chr13:49127215 | T | A | 133 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0127 others(130): Show |
133 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.253-3922T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49127215 | |||||||
| chr13:49127444 | A | G | 2 | a0001c0002t0001g0119 a0001c0002t0001g0121 |
2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.253-3693A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49127444 | |||||||
| chr13:49127603 | T | C | 117 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.253-3534T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49127603 | |||||||
| chr13:49127984 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.253-3153C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49127984 | |||||||
| chr13:49128131 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0240 a0001c0001t0006g0161 |
3 | HG02145.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.253-3006C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49128131 | |||||||
| chr13:49128353 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.253-2784G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49128353 | |||||||
| chr13:49128356 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.253-2781C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49128356 | |||||||
| chr13:49128360 | C | T | 2 | a0001c0001t0001g0124 a0005c0008t0001g0123 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.253-2777C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49128360 | |||||||
| chr13:49128420 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.253-2717G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49128420 | |||||||
| chr13:49128647 | C | A | 30 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0075 others(27): Show |
30 | HG00639.hp1 HG00733.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.253-2490C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49128647 | |||||||
| chr13:49129186 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.253-1951A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49129186 | |||||||
| chr13:49129294 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
13 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.253-1843A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49129294 | |||||||
| chr13:49129754 | G | C | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.253-1383G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49129754 | |||||||
| chr13:49129762 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.253-1375A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49129762 | |||||||
| chr13:49129936 | C | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.253-1201C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49129936 | |||||||
| chr13:49129999 | T | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.253-1138T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49129999 | |||||||
| chr13:49130258 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.253-879G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49130258 | |||||||
| chr13:49130367 | G | T | 1 | a0001c0001t0010g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.253-770G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49130367 | |||||||
| chr13:49130390 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-747A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49130390 | |||||||
| chr13:49130429 | T | G | 1 | a0001c0001t0001g0205 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.253-708T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49130429 | |||||||
| chr13:49130483 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.253-654A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49130483 | |||||||
| chr13:49130509 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.253-628C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49130509 | |||||||
| chr13:49130625 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.253-512T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49130625 | |||||||
| chr13:49130766 | TTTTTA | T | 7 | a0001c0001t0001g0292 a0002c0003t0001g0002 a0002c0003t0001g0003 others(4): Show |
7 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-356_253-352del others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr13 | 49130766 | ||||||
| chr13:49131034 | G | C | 1 | a0006c0006t0001g0074 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.253-103G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 4/25 | chr13 | 49131034 | |||||||
| chr13:49131391 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.490+17T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49131391 | |||||||
| chr13:49131639 | T | C | 5 | a0003c0004t0001g0028 a0003c0004t0001g0031 a0003c0004t0001g0035 others(2): Show |
5 | HG00280.hp2 HG01515.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+265T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49131639 | |||||||
| chr13:49131719 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.490+345T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49131719 | |||||||
| chr13:49131809 | GAAAGTTA others(6): Show |
G | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.490+450_490+462del others(13): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr13 | 49131809 | ||||||
| chr13:49132099 | C | A | 1 | a0001c0001t0001g0248 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.490+725C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49132099 | |||||||
| chr13:49132635 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.490+1261A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49132635 | |||||||
| chr13:49132827 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.490+1453T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49132827 | |||||||
| chr13:49132849 | T | G | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490+1475T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49132849 | |||||||
| chr13:49132913 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.490+1539C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49132913 | |||||||
| chr13:49132980 | G | A | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490+1606G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49132980 | |||||||
| chr13:49133080 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.490+1706A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49133080 | |||||||
| chr13:49133719 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0208 |
2 | NA18948.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.490+2345A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49133719 | |||||||
| chr13:49133726 | A | G | 1 | a0001c0002t0001g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.490+2352A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49133726 | |||||||
| chr13:49133746 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.490+2372A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49133746 | |||||||
| chr13:49133757 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.490+2383C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49133757 | |||||||
| chr13:49134185 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.491-2147G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49134185 | |||||||
| chr13:49134682 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0077 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-1650G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49134682 | |||||||
| chr13:49134767 | A | G | 120 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
120 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.491-1565A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49134767 | |||||||
| chr13:49134801 | C | CT | 9 | a0001c0001t0001g0239 a0001c0001t0001g0257 a0001c0001t0001g0267 others(6): Show |
9 | HG00733.hp1 HG00741.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.491-1508dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr13 | 49134801 | ||||||
| chr13:49134801 | CT | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(92): Show |
95 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.491-1508delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr13 | 49134801 | ||||||
| chr13:49134801 | CTT | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0080 others(13): Show |
16 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.491-1509_491-1508d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr13 | 49134801 | ||||||
| chr13:49134801 | CTTT | C | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.491-1510_491-1508d others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr13 | 49134801 | ||||||
| chr13:49134841 | C | CT | 161 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(158): Show |
161 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.491-1466dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr13 | 49134841 | ||||||
| chr13:49134841 | C | CTT | 69 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0040 others(66): Show |
69 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.491-1467_491-1466d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr13 | 49134841 | ||||||
| chr13:49134841 | C | CTTT | 24 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0050 others(21): Show |
24 | HG00438.hp1 HG00438.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.491-1468_491-1466d others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr13 | 49134841 | ||||||
| chr13:49134841 | CT | C | 16 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(13): Show |
16 | HG00741.hp2 NA18906.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.491-1466delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr13 | 49134841 | ||||||
| chr13:49134879 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0069 |
2 | HG00544.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.491-1453C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49134879 | |||||||
| chr13:49134997 | A | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0061 others(6): Show |
9 | HG00544.hp1 HG02074.hp2 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.491-1335A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49134997 | |||||||
| chr13:49135129 | A | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0240 a0001c0001t0006g0161 |
3 | HG02145.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.491-1203A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135129 | |||||||
| chr13:49135135 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.491-1197G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135135 | |||||||
| chr13:49135146 | C | A | 1 | a0007c0009t0001g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.491-1186C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135146 | |||||||
| chr13:49135320 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.491-1012C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135320 | |||||||
| chr13:49135417 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.491-915A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135417 | |||||||
| chr13:49135441 | A | G | 106 | a0001c0001t0001g0008 a0001c0001t0001g0162 a0001c0001t0001g0163 others(103): Show |
106 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.491-891A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135441 | |||||||
| chr13:49135442 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.491-890C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135442 | |||||||
| chr13:49135463 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.491-869T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135463 | |||||||
| chr13:49135514 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.491-818G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135514 | |||||||
| chr13:49135653 | T | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0146 |
2 | NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.491-679T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135653 | |||||||
| chr13:49135982 | G | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0072 |
2 | HG02074.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.491-350G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49135982 | |||||||
| chr13:49136271 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.491-61A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 5/25 | chr13 | 49136271 | |||||||
| chr13:49136850 | C | T | 138 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0127 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.760+249C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49136850 | |||||||
| chr13:49136874 | T | G | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.760+273T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49136874 | |||||||
| chr13:49137052 | C | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
13 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.760+451C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137052 | |||||||
| chr13:49137117 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.760+516G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137117 | |||||||
| chr13:49137240 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
13 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.760+639A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137240 | |||||||
| chr13:49137327 | T | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.760+726T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137327 | |||||||
| chr13:49137328 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.760+727T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137328 | |||||||
| chr13:49137584 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.760+983G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137584 | |||||||
| chr13:49137691 | A | T | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.761-1056A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137691 | |||||||
| chr13:49137734 | T | A | 1 | a0001c0001t0010g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.761-1013T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137734 | |||||||
| chr13:49137752 | T | A | 1 | a0001c0001t0001g0252 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.761-995T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137752 | |||||||
| chr13:49137777 | G | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.761-970G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137777 | |||||||
| chr13:49137834 | C | T | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.761-913C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137834 | |||||||
| chr13:49137918 | A | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.761-829A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49137918 | |||||||
| chr13:49138145 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.761-602A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49138145 | |||||||
| chr13:49138222 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.761-525C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49138222 | |||||||
| chr13:49138534 | G | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0240 a0001c0001t0006g0161 |
3 | HG02145.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.761-213G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49138534 | |||||||
| chr13:49138718 | T | A | 1 | a0001c0001t0001g0289 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.761-29T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 6/25 | chr13 | 49138718 | |||||||
| chr13:49139271 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+466A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49139271 | |||||||
| chr13:49139715 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.819+910A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49139715 | |||||||
| chr13:49139809 | C | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.819+1004C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49139809 | |||||||
| chr13:49139820 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.819+1015G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49139820 | |||||||
| chr13:49140086 | C | T | 1 | a0001c0002t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.819+1281C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49140086 | |||||||
| chr13:49140305 | C | T | 6 | a0001c0001t0001g0136 a0001c0001t0001g0140 a0001c0001t0001g0142 others(3): Show |
6 | NA18948.hp2 NA18973.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+1500C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49140305 | |||||||
| chr13:49140907 | C | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.819+2102C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49140907 | |||||||
| chr13:49141434 | G | C | 1 | a0001c0001t0001g0273 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.819+2629G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49141434 | |||||||
| chr13:49141522 | T | C | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.819+2717T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49141522 | |||||||
| chr13:49141813 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.819+3008C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49141813 | |||||||
| chr13:49141945 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.819+3140C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49141945 | |||||||
| chr13:49142141 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.819+3336G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49142141 | |||||||
| chr13:49142273 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.819+3468C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49142273 | |||||||
| chr13:49142540 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-3238A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49142540 | |||||||
| chr13:49142782 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.820-2996A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49142782 | |||||||
| chr13:49142818 | T | G | 1 | a0001c0001t0006g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.820-2960T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49142818 | |||||||
| chr13:49142844 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
13 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.820-2934A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49142844 | |||||||
| chr13:49142856 | A | C | 1 | a0001c0002t0001g0117 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.820-2922A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49142856 | |||||||
| chr13:49143304 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.820-2474G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49143304 | |||||||
| chr13:49143316 | G | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.820-2462G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49143316 | |||||||
| chr13:49143361 | T | TA | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(10): Show |
13 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.820-2410dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 49143361 | ||||||
| chr13:49143415 | T | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0021 others(3): Show |
6 | HG01167.hp2 HG01175.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.820-2363T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49143415 | |||||||
| chr13:49143433 | A | G | 8 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(5): Show |
8 | NA18612.hp2 NA18939.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.820-2345A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49143433 | |||||||
| chr13:49143681 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.820-2097G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49143681 | |||||||
| chr13:49143765 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.820-2013A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49143765 | |||||||
| chr13:49143978 | T | TTAC | 17 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0096 others(14): Show |
17 | HG01074.hp2 HG01175.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.820-1768_820-1766d others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 49143978 | ||||||
| chr13:49143978 | T | TTACTAC | 89 | a0001c0001t0001g0008 a0001c0001t0001g0091 a0001c0001t0001g0163 others(86): Show |
89 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.820-1771_820-1766d others(8): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 49143978 | ||||||
| chr13:49143978 | T | TTACTACT others(2): Show |
15 | a0001c0001t0001g0188 a0001c0001t0001g0209 a0001c0001t0001g0212 others(12): Show |
15 | HG01978.hp2 HG02074.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.820-1774_820-1766d others(11): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 49143978 | ||||||
| chr13:49143978 | T | TTACTACT others(5): Show |
1 | a0001c0001t0001g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.820-1777_820-1766d others(14): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 49143978 | ||||||
| chr13:49143978 | T | TTACTACT others(8): Show |
1 | a0001c0001t0001g0263 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.820-1780_820-1766d others(17): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 49143978 | ||||||
| chr13:49144013 | G | A | 7 | a0001c0001t0001g0187 a0002c0003t0001g0002 a0002c0003t0001g0003 others(4): Show |
7 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-1765G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144013 | |||||||
| chr13:49144025 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-1753A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144025 | |||||||
| chr13:49144032 | C | A | 10 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0052 others(7): Show |
10 | HG01168.hp2 HG01515.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.820-1746C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144032 | |||||||
| chr13:49144035 | A | C | 154 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0024 others(151): Show |
154 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.820-1743A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144035 | |||||||
| chr13:49144038 | A | C | 20 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(17): Show |
20 | HG03209.hp2 HG03704.hp2 NA18944.hp1 others(17): Show |
intron_variant | MODIFIER | c.820-1740A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144038 | |||||||
| chr13:49144188 | T | A | 1 | a0001c0001t0001g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.820-1590T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144188 | |||||||
| chr13:49144200 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.820-1578G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144200 | |||||||
| chr13:49144531 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.820-1247T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144531 | |||||||
| chr13:49144697 | A | G | 120 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
120 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.820-1081A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144697 | |||||||
| chr13:49144735 | C | T | 129 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(126): Show |
129 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.820-1043C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144735 | |||||||
| chr13:49144924 | A | G | 16 | a0001c0001t0001g0168 a0001c0001t0001g0245 a0001c0001t0001g0247 others(13): Show |
16 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.820-854A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144924 | |||||||
| chr13:49144943 | T | A | 1 | a0001c0005t0001g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.820-835T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | chr13 | 49144943 | |||||||
| chr13:49144944 | C | CT | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-828dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr13 | 49144944 | ||||||
| chr13:49146030 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.977+95C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146030 | |||||||
| chr13:49146271 | T | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.977+336T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146271 | |||||||
| chr13:49146298 | C | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0228 |
2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.977+363C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146298 | |||||||
| chr13:49146531 | G | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.977+596G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146531 | |||||||
| chr13:49146693 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.977+758C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146693 | |||||||
| chr13:49146756 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.977+821A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146756 | |||||||
| chr13:49146767 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.977+832C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146767 | |||||||
| chr13:49146803 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0146 |
2 | NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.977+868C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146803 | |||||||
| chr13:49146844 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.977+909A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146844 | |||||||
| chr13:49146850 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.977+915A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146850 | |||||||
| chr13:49146899 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.977+964T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49146899 | |||||||
| chr13:49147369 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG00438.hp1 HG01081.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.977+1434C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147369 | |||||||
| chr13:49147552 | G | A | 2 | a0001c0001t0001g0063 a0001c0002t0001g0009 |
2 | HG02055.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.977+1617G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147552 | |||||||
| chr13:49147554 | A | T | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+1619A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147554 | |||||||
| chr13:49147555 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+1620T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147555 | |||||||
| chr13:49147557 | G | C | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+1622G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147557 | |||||||
| chr13:49147558 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+1623G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147558 | |||||||
| chr13:49147561 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+1626G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147561 | |||||||
| chr13:49147563 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+1628T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147563 | |||||||
| chr13:49147565 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+1630T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147565 | |||||||
| chr13:49147569 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+1634G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147569 | |||||||
| chr13:49147570 | C | G | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+1635C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147570 | |||||||
| chr13:49147572 | A | T | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+1637A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147572 | |||||||
| chr13:49147702 | A | C | 9 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(6): Show |
9 | HG01433.hp2 HG01928.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.977+1767A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147702 | |||||||
| chr13:49147704 | A | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.977+1769A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147704 | |||||||
| chr13:49147781 | A | AT | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.977+1851dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr13 | 49147781 | ||||||
| chr13:49147834 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.977+1899T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147834 | |||||||
| chr13:49147986 | A | C | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.977+2051A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49147986 | |||||||
| chr13:49148138 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+2203G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49148138 | |||||||
| chr13:49148146 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.977+2211A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49148146 | |||||||
| chr13:49148228 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0147 |
2 | NA18985.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.977+2293A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49148228 | |||||||
| chr13:49148352 | C | CATTTA | 15 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(12): Show |
15 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.977+2419_977+2423d others(7): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr13 | 49148352 | ||||||
| chr13:49148495 | C | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.977+2560C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49148495 | |||||||
| chr13:49148689 | T | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.977+2754T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49148689 | |||||||
| chr13:49149006 | T | G | 1 | a0001c0001t0001g0275 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.977+3071T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49149006 | |||||||
| chr13:49149199 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.977+3264C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49149199 | |||||||
| chr13:49149253 | G | T | 2 | a0001c0001t0001g0227 a0001c0001t0007g0225 |
2 | NA18953.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.977+3318G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49149253 | |||||||
| chr13:49149331 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.977+3396A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49149331 | |||||||
| chr13:49149393 | G | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.977+3458G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49149393 | |||||||
| chr13:49149561 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.977+3626T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49149561 | |||||||
| chr13:49149898 | G | A | 3 | a0001c0002t0001g0119 a0001c0002t0001g0120 a0001c0002t0001g0121 |
3 | HG02723.hp2 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.977+3963G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49149898 | |||||||
| chr13:49149951 | G | C | 1 | a0001c0001t0001g0237 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.977+4016G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49149951 | |||||||
| chr13:49150136 | G | A | 11 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(8): Show |
11 | HG02015.hp2 NA18612.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.977+4201G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49150136 | |||||||
| chr13:49150273 | C | T | 13 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(10): Show |
13 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.977+4338C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49150273 | |||||||
| chr13:49150477 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0242 |
3 | HG02630.hp1 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.977+4542G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49150477 | |||||||
| chr13:49150484 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0078 |
3 | HG01070.hp1 HG01071.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.977+4549G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49150484 | |||||||
| chr13:49150632 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.977+4697A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49150632 | |||||||
| chr13:49150712 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.977+4777C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49150712 | |||||||
| chr13:49150713 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.977+4778G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49150713 | |||||||
| chr13:49150817 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.977+4882C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49150817 | |||||||
| chr13:49150943 | C | CA | 53 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0029 others(50): Show |
53 | HG00741.hp2 HG01074.hp2 HG01257.hp1 others(50): Show |
intron_variant | MODIFIER | c.977+5029dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr13 | 49150943 | ||||||
| chr13:49150943 | CA | C | 116 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0068 others(113): Show |
116 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.977+5029delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr13 | 49150943 | ||||||
| chr13:49150943 | CAA | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0206 a0001c0001t0001g0222 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.977+5028_977+5029d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr13 | 49150943 | ||||||
| chr13:49151117 | A | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.977+5182A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49151117 | |||||||
| chr13:49151292 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.977+5357T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49151292 | |||||||
| chr13:49151431 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.977+5496C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49151431 | |||||||
| chr13:49151623 | C | T | 117 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.977+5688C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49151623 | |||||||
| chr13:49151650 | T | G | 18 | a0001c0002t0001g0009 a0001c0002t0001g0057 a0001c0002t0001g0085 others(15): Show |
18 | HG01496.hp2 HG02055.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.977+5715T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49151650 | |||||||
| chr13:49151651 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.977+5716G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49151651 | |||||||
| chr13:49151769 | G | A | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.977+5834G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49151769 | |||||||
| chr13:49151875 | A | G | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.977+5940A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49151875 | |||||||
| chr13:49151886 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG00438.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.977+5951T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49151886 | |||||||
| chr13:49151889 | G | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.977+5954G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49151889 | |||||||
| chr13:49152287 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.977+6352G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49152287 | |||||||
| chr13:49152401 | C | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.977+6466C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49152401 | |||||||
| chr13:49152512 | G | GT | 117 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.977+6577_977+6578i others(3): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49152512 | |||||||
| chr13:49152522 | T | A | 1 | a0001c0001t0001g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.977+6587T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49152522 | |||||||
| chr13:49152535 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.977+6600A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49152535 | |||||||
| chr13:49152662 | T | C | 1 | a0003c0004t0001g0028 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.977+6727T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49152662 | |||||||
| chr13:49152746 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0101 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.977+6811C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49152746 | |||||||
| chr13:49152759 | A | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0240 a0001c0001t0006g0161 |
3 | HG02145.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.977+6824A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49152759 | |||||||
| chr13:49152780 | G | A | 5 | a0001c0001t0001g0186 a0001c0001t0001g0197 a0001c0001t0001g0224 others(2): Show |
5 | HG02257.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.977+6845G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49152780 | |||||||
| chr13:49152958 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18943.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.977+7023G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49152958 | |||||||
| chr13:49153014 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.977+7079A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153014 | |||||||
| chr13:49153068 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.977+7133C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153068 | |||||||
| chr13:49153089 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.977+7154G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153089 | |||||||
| chr13:49153132 | A | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.977+7197A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153132 | |||||||
| chr13:49153192 | C | G | 1 | a0001c0001t0001g0027 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.977+7257C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153192 | |||||||
| chr13:49153237 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.977+7302T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153237 | |||||||
| chr13:49153275 | A | G | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG01891.hp1 HG02698.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.977+7340A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153275 | |||||||
| chr13:49153284 | T | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
13 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.977+7349T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153284 | |||||||
| chr13:49153442 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0001g0285 |
3 | HG02109.hp2 HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.977+7507C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153442 | |||||||
| chr13:49153443 | A | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0274 a0001c0001t0001g0285 |
3 | HG02109.hp2 HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.977+7508A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153443 | |||||||
| chr13:49153547 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.977+7612C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153547 | |||||||
| chr13:49153718 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.977+7783G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153718 | |||||||
| chr13:49153733 | A | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG00438.hp1 HG01081.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.977+7798A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153733 | |||||||
| chr13:49153922 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.977+7987C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49153922 | |||||||
| chr13:49154007 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG00438.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.977+8072T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154007 | |||||||
| chr13:49154178 | A | G | 1 | a0003c0004t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.977+8243A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154178 | |||||||
| chr13:49154315 | CTGTT | C | 98 | a0001c0001t0001g0008 a0001c0001t0001g0162 a0001c0001t0001g0163 others(95): Show |
98 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.977+8384_977+8387d others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr13 | 49154315 | ||||||
| chr13:49154457 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.977+8522G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154457 | |||||||
| chr13:49154495 | C | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.977+8560C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154495 | |||||||
| chr13:49154526 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0234 |
2 | NA18944.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.977+8591A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154526 | |||||||
| chr13:49154568 | T | C | 1 | a0007c0009t0001g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.977+8633T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154568 | |||||||
| chr13:49154576 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.977+8641G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154576 | |||||||
| chr13:49154581 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.977+8646C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154581 | |||||||
| chr13:49154635 | A | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0240 a0001c0001t0006g0161 |
3 | HG02145.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.977+8700A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154635 | |||||||
| chr13:49154636 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.977+8701G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154636 | |||||||
| chr13:49154729 | G | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.977+8794G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154729 | |||||||
| chr13:49154765 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.977+8830A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49154765 | |||||||
| chr13:49155065 | A | G | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.977+9130A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155065 | |||||||
| chr13:49155107 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.977+9172T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155107 | |||||||
| chr13:49155118 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.977+9183A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155118 | |||||||
| chr13:49155146 | C | T | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.977+9211C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155146 | |||||||
| chr13:49155249 | G | A | 1 | a0001c0005t0001g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.977+9314G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155249 | |||||||
| chr13:49155324 | C | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.977+9389C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155324 | |||||||
| chr13:49155383 | T | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.977+9448T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155383 | |||||||
| chr13:49155384 | TG | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
13 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.977+9450delG | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155384 | |||||||
| chr13:49155385 | G | T | 138 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0127 others(135): Show |
138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.977+9450G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155385 | |||||||
| chr13:49155435 | G | A | 120 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
120 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.977+9500G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155435 | |||||||
| chr13:49155503 | T | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.977+9568T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155503 | |||||||
| chr13:49155595 | A | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0226 a0001c0001t0001g0227 others(6): Show |
9 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.977+9660A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155595 | |||||||
| chr13:49155653 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00621.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.977+9718A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155653 | |||||||
| chr13:49155731 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.977+9796G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155731 | |||||||
| chr13:49155885 | T | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
13 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.977+9950T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155885 | |||||||
| chr13:49155899 | G | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.977+9964G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49155899 | |||||||
| chr13:49156037 | C | T | 129 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(126): Show |
129 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.977+10102C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49156037 | |||||||
| chr13:49156172 | T | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.977+10237T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49156172 | |||||||
| chr13:49156175 | A | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.977+10240A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49156175 | |||||||
| chr13:49156651 | G | A | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.978-10593G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49156651 | |||||||
| chr13:49156683 | G | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.978-10561G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49156683 | |||||||
| chr13:49156774 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.978-10470T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49156774 | |||||||
| chr13:49156777 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978-10467T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49156777 | |||||||
| chr13:49156879 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.978-10365C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49156879 | |||||||
| chr13:49156936 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.978-10308C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49156936 | |||||||
| chr13:49157063 | G | A | 83 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(80): Show |
83 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.978-10181G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157063 | |||||||
| chr13:49157280 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.978-9964A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157280 | |||||||
| chr13:49157293 | T | C | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0154 others(1): Show |
4 | HG01257.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.978-9951T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157293 | |||||||
| chr13:49157340 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.978-9904C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157340 | |||||||
| chr13:49157388 | T | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(12): Show |
15 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.978-9856T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157388 | |||||||
| chr13:49157399 | G | A | 8 | a0001c0001t0001g0075 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG00639.hp1 HG00733.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.978-9845G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157399 | |||||||
| chr13:49157531 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978-9713A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157531 | |||||||
| chr13:49157553 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.978-9691G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157553 | |||||||
| chr13:49157571 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.978-9673C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157571 | |||||||
| chr13:49157779 | C | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0126 a0001c0001t0001g0128 |
3 | HG01074.hp2 HG02055.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.978-9465C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157779 | |||||||
| chr13:49157780 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.978-9464G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157780 | |||||||
| chr13:49157780 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.978-9464G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157780 | |||||||
| chr13:49157821 | G | T | 14 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0077 others(11): Show |
14 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.978-9423G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157821 | |||||||
| chr13:49157864 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.978-9380G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157864 | |||||||
| chr13:49157875 | C | G | 4 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0223 others(1): Show |
4 | NA18959.hp1 NA18969.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.978-9369C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157875 | |||||||
| chr13:49157994 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.978-9250C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49157994 | |||||||
| chr13:49158012 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.978-9232A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158012 | |||||||
| chr13:49158049 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.978-9195T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158049 | |||||||
| chr13:49158056 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.978-9188G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158056 | |||||||
| chr13:49158064 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.978-9180C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158064 | |||||||
| chr13:49158127 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.978-9117T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158127 | |||||||
| chr13:49158128 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.978-9116C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158128 | |||||||
| chr13:49158191 | C | T | 14 | a0001c0002t0001g0009 a0001c0002t0001g0057 a0001c0002t0001g0086 others(11): Show |
14 | HG01496.hp2 HG02055.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.978-9053C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158191 | |||||||
| chr13:49158226 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.978-9018C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158226 | |||||||
| chr13:49158227 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.978-9017G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158227 | |||||||
| chr13:49158350 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.978-8894A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158350 | |||||||
| chr13:49158385 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01975.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.978-8859A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158385 | |||||||
| chr13:49158468 | A | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0122 |
3 | HG01167.hp2 HG01175.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.978-8776A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158468 | |||||||
| chr13:49158477 | TCTTCTGC others(36): Show |
T | 2 | a0001c0002t0001g0090 a0001c0002t0001g0107 |
2 | NA18954.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.978-8764_978-8722d others(45): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr13 | 49158477 | ||||||
| chr13:49158485 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.978-8759G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158485 | |||||||
| chr13:49158511 | G | A | 133 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0126 others(130): Show |
133 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.978-8733G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158511 | |||||||
| chr13:49158526 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.978-8718C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158526 | |||||||
| chr13:49158677 | T | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.978-8567T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158677 | |||||||
| chr13:49158680 | T | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.978-8564T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158680 | |||||||
| chr13:49158927 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.978-8317T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49158927 | |||||||
| chr13:49159121 | A | G | 4 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0246 others(1): Show |
4 | NA18953.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.978-8123A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159121 | |||||||
| chr13:49159136 | G | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.978-8108G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159136 | |||||||
| chr13:49159183 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.978-8061G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159183 | |||||||
| chr13:49159227 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.978-8017C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159227 | |||||||
| chr13:49159245 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.978-7999T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159245 | |||||||
| chr13:49159302 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.978-7942G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159302 | |||||||
| chr13:49159476 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.978-7768G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159476 | |||||||
| chr13:49159763 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.978-7481T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159763 | |||||||
| chr13:49159802 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.978-7442G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159802 | |||||||
| chr13:49159809 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.978-7435C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159809 | |||||||
| chr13:49159814 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.978-7430T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159814 | |||||||
| chr13:49159906 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.978-7338A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159906 | |||||||
| chr13:49159939 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.978-7305G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49159939 | |||||||
| chr13:49160000 | T | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.978-7244T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160000 | |||||||
| chr13:49160014 | G | T | 1 | a0001c0002t0001g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.978-7230G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160014 | |||||||
| chr13:49160063 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0069 |
2 | HG00544.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.978-7181A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160063 | |||||||
| chr13:49160246 | C | T | 1 | a0001c0002t0001g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.978-6998C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160246 | |||||||
| chr13:49160334 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.978-6910G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160334 | |||||||
| chr13:49160356 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.978-6888T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160356 | |||||||
| chr13:49160409 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0122 |
3 | HG01167.hp2 HG01175.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.978-6835G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160409 | |||||||
| chr13:49160559 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.978-6685C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160559 | |||||||
| chr13:49160713 | C | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.978-6531C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160713 | |||||||
| chr13:49160742 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.978-6502C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160742 | |||||||
| chr13:49160786 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.978-6458T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160786 | |||||||
| chr13:49160925 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.978-6319C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49160925 | |||||||
| chr13:49161042 | A | G | 2 | a0001c0002t0001g0090 a0001c0002t0001g0107 |
2 | NA18954.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.978-6202A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161042 | |||||||
| chr13:49161076 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.978-6168C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161076 | |||||||
| chr13:49161134 | G | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.978-6110G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161134 | |||||||
| chr13:49161136 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.978-6108C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161136 | |||||||
| chr13:49161138 | A | T | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.978-6106A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161138 | |||||||
| chr13:49161142 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.978-6102G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161142 | |||||||
| chr13:49161145 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.978-6099G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161145 | |||||||
| chr13:49161186 | T | C | 120 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
120 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.978-6058T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161186 | |||||||
| chr13:49161237 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978-6007A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161237 | |||||||
| chr13:49161507 | A | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.978-5737A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161507 | |||||||
| chr13:49161517 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.978-5727A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161517 | |||||||
| chr13:49161683 | G | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.978-5561G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161683 | |||||||
| chr13:49161751 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.978-5493C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161751 | |||||||
| chr13:49161840 | T | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.978-5404T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161840 | |||||||
| chr13:49161984 | T | A | 1 | a0007c0009t0001g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.978-5260T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49161984 | |||||||
| chr13:49162012 | C | T | 7 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0001g0197 others(4): Show |
7 | HG02257.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.978-5232C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162012 | |||||||
| chr13:49162079 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.978-5165T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162079 | |||||||
| chr13:49162129 | A | G | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.978-5115A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162129 | |||||||
| chr13:49162145 | T | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.978-5099T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162145 | |||||||
| chr13:49162279 | C | T | 4 | a0003c0004t0001g0028 a0003c0004t0001g0031 a0003c0004t0001g0035 others(1): Show |
4 | HG00280.hp2 HG01515.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.978-4965C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162279 | |||||||
| chr13:49162344 | C | T | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.978-4900C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162344 | |||||||
| chr13:49162356 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.978-4888T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162356 | |||||||
| chr13:49162395 | G | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0250 |
2 | HG00639.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.978-4849G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162395 | |||||||
| chr13:49162424 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.978-4820C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162424 | |||||||
| chr13:49162427 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.978-4817G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162427 | |||||||
| chr13:49162613 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0072 |
2 | HG02074.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.978-4631A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162613 | |||||||
| chr13:49162633 | G | A | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.978-4611G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162633 | |||||||
| chr13:49162649 | G | A | 129 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0130 others(126): Show |
129 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.978-4595G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49162649 | |||||||
| chr13:49163173 | A | G | 2 | a0001c0001t0001g0195 a0007c0009t0001g0194 |
2 | HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.978-4071A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49163173 | |||||||
| chr13:49163362 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.978-3882G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49163362 | |||||||
| chr13:49163469 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.978-3775G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49163469 | |||||||
| chr13:49163599 | A | G | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.978-3645A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49163599 | |||||||
| chr13:49163665 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.978-3579T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49163665 | |||||||
| chr13:49163788 | T | A | 4 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0223 others(1): Show |
4 | NA18959.hp1 NA18969.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.978-3456T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49163788 | |||||||
| chr13:49164523 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.978-2721G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49164523 | |||||||
| chr13:49164771 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.978-2473G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49164771 | |||||||
| chr13:49164810 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.978-2434C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49164810 | |||||||
| chr13:49164866 | G | A | 1 | a0003c0004t0001g0045 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.978-2378G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49164866 | |||||||
| chr13:49165056 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.978-2188T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49165056 | |||||||
| chr13:49165232 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978-2012C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49165232 | |||||||
| chr13:49165614 | A | T | 11 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(8): Show |
11 | HG02015.hp2 NA18612.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.978-1630A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49165614 | |||||||
| chr13:49165991 | T | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.978-1253T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49165991 | |||||||
| chr13:49166143 | T | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.978-1101T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49166143 | |||||||
| chr13:49166417 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.978-827G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49166417 | |||||||
| chr13:49166563 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.978-681A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49166563 | |||||||
| chr13:49166571 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.978-673C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49166571 | |||||||
| chr13:49166720 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0039 others(2): Show |
5 | NA18956.hp2 NA18998.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.978-524C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49166720 | |||||||
| chr13:49166752 | T | C | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.978-492T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49166752 | |||||||
| chr13:49166983 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.978-261T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49166983 | |||||||
| chr13:49166990 | C | CA | 127 | a0001c0001t0001g0008 a0001c0001t0001g0132 a0001c0001t0001g0133 others(124): Show |
127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.978-246dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr13 | 49166990 | ||||||
| chr13:49167013 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.978-231C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49167013 | |||||||
| chr13:49167197 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0131 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.978-47A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 8/25 | chr13 | 49167197 | |||||||
| chr13:49167349 | G | T | 2 | a0002c0003t0001g0004 a0002c0003t0001g0005 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1037+46G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 9/25 | chr13 | 49167349 | |||||||
| chr13:49167445 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1037+142G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 9/25 | chr13 | 49167445 | |||||||
| chr13:49167516 | G | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037+213G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 9/25 | chr13 | 49167516 | |||||||
| chr13:49167534 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1037+231A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 9/25 | chr13 | 49167534 | |||||||
| chr13:49167564 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1037+261A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 9/25 | chr13 | 49167564 | |||||||
| chr13:49167592 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1037+289G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 9/25 | chr13 | 49167592 | |||||||
| chr13:49167709 | CA | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037+417delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr13 | 49167709 | ||||||
| chr13:49167768 | CA | C | 13 | a0001c0002t0001g0009 a0001c0002t0001g0057 a0001c0002t0001g0086 others(10): Show |
13 | HG01496.hp2 HG02055.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1037+475delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr13 | 49167768 | ||||||
| chr13:49168762 | TC | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1176+12delC | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49168762 | |||||||
| chr13:49168926 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0261 |
2 | HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1176+175C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49168926 | |||||||
| chr13:49168952 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1176+201C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49168952 | |||||||
| chr13:49168955 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0228 |
2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1176+204T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49168955 | |||||||
| chr13:49169110 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1176+359T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49169110 | |||||||
| chr13:49169443 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1176+692T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49169443 | |||||||
| chr13:49169514 | G | A | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1176+763G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49169514 | |||||||
| chr13:49169590 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1176+839A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49169590 | |||||||
| chr13:49169633 | C | T | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1176+882C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49169633 | |||||||
| chr13:49169732 | A | T | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1176+981A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49169732 | |||||||
| chr13:49169900 | T | A | 47 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(44): Show |
47 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1176+1149T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49169900 | |||||||
| chr13:49170160 | A | G | 68 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(65): Show |
68 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1176+1409A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49170160 | |||||||
| chr13:49170199 | T | C | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.1176+1448T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49170199 | |||||||
| chr13:49170259 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1176+1508G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49170259 | |||||||
| chr13:49170289 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG00438.hp1 HG01081.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1176+1538C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49170289 | |||||||
| chr13:49170432 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1177-1611A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49170432 | |||||||
| chr13:49170547 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1177-1496C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49170547 | |||||||
| chr13:49170667 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1177-1376G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49170667 | |||||||
| chr13:49170766 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1177-1277A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49170766 | |||||||
| chr13:49170938 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1177-1105G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49170938 | |||||||
| chr13:49171043 | C | T | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1177-1000C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49171043 | |||||||
| chr13:49171397 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1177-646G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49171397 | |||||||
| chr13:49171398 | A | T | 1 | a0001c0001t0001g0278 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1177-645A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49171398 | |||||||
| chr13:49171763 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
13 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.1177-280A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49171763 | |||||||
| chr13:49171779 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1177-264C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49171779 | |||||||
| chr13:49171897 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1177-146T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 10/25 | chr13 | 49171897 | |||||||
| chr13:49172235 | G | T | 2 | a0002c0003t0001g0004 a0002c0003t0001g0005 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1230+139G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49172235 | |||||||
| chr13:49172253 | A | C | 1 | a0001c0001t0001g0290 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1230+157A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49172253 | |||||||
| chr13:49172350 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+254G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49172350 | |||||||
| chr13:49172385 | C | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0239 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1230+289C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49172385 | |||||||
| chr13:49172461 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1230+365A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49172461 | |||||||
| chr13:49172560 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1230+464G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49172560 | |||||||
| chr13:49172582 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(270): Show |
273 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.1230+486A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49172582 | |||||||
| chr13:49172583 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1230+487T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49172583 | |||||||
| chr13:49172776 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1230+680T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49172776 | |||||||
| chr13:49172815 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1230+719G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49172815 | |||||||
| chr13:49173094 | CTGGGCCG others(11): Show |
C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1230+1008_1230+102 others(22): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr13 | 49173094 | ||||||
| chr13:49173240 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1230+1144A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49173240 | |||||||
| chr13:49173304 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0066 a0006c0006t0001g0074 |
3 | NA18951.hp2 NA18962.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1231-1131G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49173304 | |||||||
| chr13:49173410 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1231-1025A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49173410 | |||||||
| chr13:49173472 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1231-963T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49173472 | |||||||
| chr13:49173800 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1231-635A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49173800 | |||||||
| chr13:49173839 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1231-596C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49173839 | |||||||
| chr13:49174083 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1231-352C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49174083 | |||||||
| chr13:49174144 | A | G | 4 | a0003c0004t0001g0028 a0003c0004t0001g0031 a0003c0004t0001g0035 others(1): Show |
4 | HG00280.hp2 HG01515.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-291A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49174144 | |||||||
| chr13:49174149 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1231-286A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49174149 | |||||||
| chr13:49174176 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1231-259A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49174176 | |||||||
| chr13:49174187 | A | C | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.1231-248A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49174187 | |||||||
| chr13:49174293 | A | T | 10 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0171 others(7): Show |
10 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-142A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 11/25 | chr13 | 49174293 | |||||||
| chr13:49174880 | C | T | 2 | a0001c0001t0001g0195 a0007c0009t0001g0194 |
2 | HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1355+321C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 12/25 | chr13 | 49174880 | |||||||
| chr13:49174940 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0022 |
2 | NA18942.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1355+381T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 12/25 | chr13 | 49174940 | |||||||
| chr13:49174961 | T | G | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1355+402T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 12/25 | chr13 | 49174961 | |||||||
| chr13:49174983 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1356-384G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 12/25 | chr13 | 49174983 | |||||||
| chr13:49175006 | T | TA | 67 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
67 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1356-360dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr13 | 49175006 | ||||||
| chr13:49175008 | C | T | 13 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(10): Show |
13 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1356-359C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 12/25 | chr13 | 49175008 | |||||||
| chr13:49175088 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1356-279T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 12/25 | chr13 | 49175088 | |||||||
| chr13:49175768 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0125 others(9): Show |
12 | HG01257.hp1 HG01891.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.1530+227A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49175768 | |||||||
| chr13:49175898 | T | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1530+357T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49175898 | |||||||
| chr13:49175924 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1530+383C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49175924 | |||||||
| chr13:49175944 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1530+403A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49175944 | |||||||
| chr13:49175988 | A | G | 7 | a0001c0001t0001g0168 a0001c0001t0001g0253 a0001c0001t0001g0254 others(4): Show |
7 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+447A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49175988 | |||||||
| chr13:49175997 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1530+456G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49175997 | |||||||
| chr13:49176244 | G | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(9): Show |
12 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1530+703G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49176244 | |||||||
| chr13:49176457 | G | C | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1530+916G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49176457 | |||||||
| chr13:49176545 | T | A | 1 | a0001c0001t0002g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1530+1004T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49176545 | |||||||
| chr13:49176822 | A | G | 14 | a0001c0002t0001g0009 a0001c0002t0001g0057 a0001c0002t0001g0086 others(11): Show |
14 | HG01496.hp2 HG02055.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1530+1281A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49176822 | |||||||
| chr13:49177156 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1531-1412A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49177156 | |||||||
| chr13:49177252 | T | C | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG02132.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1531-1316T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49177252 | |||||||
| chr13:49177287 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1531-1281G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49177287 | |||||||
| chr13:49177328 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.1531-1240G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49177328 | |||||||
| chr13:49177536 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1531-1032A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49177536 | |||||||
| chr13:49177780 | C | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1531-788C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49177780 | |||||||
| chr13:49177964 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1531-604A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49177964 | |||||||
| chr13:49178054 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0250 |
2 | HG00639.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1531-514C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49178054 | |||||||
| chr13:49178195 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1531-373A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49178195 | |||||||
| chr13:49178284 | C | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1531-284C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49178284 | |||||||
| chr13:49178318 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1531-250G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49178318 | |||||||
| chr13:49178403 | C | G | 2 | a0001c0001t0001g0124 a0005c0008t0001g0123 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1531-165C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 13/25 | chr13 | 49178403 | |||||||
| chr13:49178678 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1617+24G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49178678 | |||||||
| chr13:49178779 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.1617+125A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49178779 | |||||||
| chr13:49178942 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0124 others(148): Show |
151 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1617+288A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49178942 | |||||||
| chr13:49179036 | A | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1617+382A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49179036 | |||||||
| chr13:49179233 | TACTA | T | 120 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
120 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1617+581_1617+584d others(6): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 49179233 | ||||||
| chr13:49179360 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0005c0008t0001g0123 |
3 | HG01257.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1617+706A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49179360 | |||||||
| chr13:49179401 | ATTC | A | 4 | a0001c0001t0001g0212 a0001c0001t0001g0233 a0001c0001t0001g0241 others(1): Show |
4 | HG02074.hp1 HG02132.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617+750_1617+752d others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 49179401 | ||||||
| chr13:49179593 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1617+939G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49179593 | |||||||
| chr13:49179648 | G | A | 1 | a0001c0001t0010g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1617+994G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49179648 | |||||||
| chr13:49179862 | C | G | 6 | a0001c0001t0001g0168 a0001c0001t0001g0254 a0001c0001t0001g0255 others(3): Show |
6 | HG01106.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1617+1208C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49179862 | |||||||
| chr13:49180218 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0018 |
2 | NA18968.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1617+1564A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49180218 | |||||||
| chr13:49180554 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1617+1900T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49180554 | |||||||
| chr13:49180731 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1617+2077A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49180731 | |||||||
| chr13:49180787 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1617+2133C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49180787 | |||||||
| chr13:49180866 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617+2212G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49180866 | |||||||
| chr13:49180939 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1617+2285A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49180939 | |||||||
| chr13:49181295 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1617+2641G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49181295 | |||||||
| chr13:49181355 | G | A | 1 | a0005c0008t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1617+2701G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49181355 | |||||||
| chr13:49181508 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1617+2854C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49181508 | |||||||
| chr13:49181710 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1617+3056C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49181710 | |||||||
| chr13:49181763 | AT | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617+3110delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49181763 | |||||||
| chr13:49181944 | A | C | 1 | a0001c0001t0001g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1617+3290A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49181944 | |||||||
| chr13:49181965 | G | A | 1 | a0001c0002t0001g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1617+3311G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49181965 | |||||||
| chr13:49181991 | G | C | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1617+3337G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49181991 | |||||||
| chr13:49182224 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617+3570A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49182224 | |||||||
| chr13:49182570 | T | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1618-3394T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49182570 | |||||||
| chr13:49183175 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1618-2789A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49183175 | |||||||
| chr13:49183301 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1618-2663T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49183301 | |||||||
| chr13:49183753 | C | T | 117 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1618-2211C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49183753 | |||||||
| chr13:49183860 | G | A | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1618-2104G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49183860 | |||||||
| chr13:49184009 | A | G | 139 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0127 others(136): Show |
139 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1618-1955A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49184009 | |||||||
| chr13:49184245 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1618-1719T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49184245 | |||||||
| chr13:49184358 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1618-1606T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49184358 | |||||||
| chr13:49184362 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1618-1602C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49184362 | |||||||
| chr13:49184497 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1618-1467G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49184497 | |||||||
| chr13:49184870 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.1618-1094A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49184870 | |||||||
| chr13:49185133 | TGAG | T | 114 | a0001c0001t0001g0008 a0001c0001t0001g0162 a0001c0001t0001g0163 others(111): Show |
114 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1618-828_1618-826d others(5): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr13 | 49185133 | ||||||
| chr13:49185369 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1618-595A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49185369 | |||||||
| chr13:49185429 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1618-535C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49185429 | |||||||
| chr13:49185491 | C | A | 17 | a0001c0002t0001g0009 a0001c0002t0001g0057 a0001c0002t0001g0086 others(14): Show |
17 | HG01496.hp2 HG02055.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.1618-473C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49185491 | |||||||
| chr13:49185620 | A | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0240 a0001c0001t0006g0161 |
3 | HG02145.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1618-344A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49185620 | |||||||
| chr13:49185752 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1618-212G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 14/25 | chr13 | 49185752 | |||||||
| chr13:49186140 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1756+38C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 15/25 | chr13 | 49186140 | |||||||
| chr13:49186235 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1756+133T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 15/25 | chr13 | 49186235 | |||||||
| chr13:49186268 | ACT | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.1756+170_1756+171d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr13 | 49186268 | ||||||
| chr13:49186401 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1756+299C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 15/25 | chr13 | 49186401 | |||||||
| chr13:49186530 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.1756+428G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 15/25 | chr13 | 49186530 | |||||||
| chr13:49186941 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1757-181A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 15/25 | chr13 | 49186941 | |||||||
| chr13:49187078 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1757-44G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 15/25 | chr13 | 49187078 | |||||||
| chr13:49187651 | C | T | 117 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1825+461C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 16/25 | chr13 | 49187651 | |||||||
| chr13:49187780 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1825+590C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 16/25 | chr13 | 49187780 | |||||||
| chr13:49187782 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1825+592G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 16/25 | chr13 | 49187782 | |||||||
| chr13:49187898 | A | G | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1826-617A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 16/25 | chr13 | 49187898 | |||||||
| chr13:49188820 | C | T | 117 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1944+187C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49188820 | |||||||
| chr13:49189185 | C | CAG | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(268): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.1944+553_1944+554d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 49189185 | ||||||
| chr13:49189417 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1944+784G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49189417 | |||||||
| chr13:49189471 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0061 others(6): Show |
9 | HG00544.hp1 HG02074.hp2 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.1944+838G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49189471 | |||||||
| chr13:49189547 | G | GT | 6 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(3): Show |
6 | HG01891.hp2 HG02135.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.1944+924dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 49189547 | ||||||
| chr13:49189549 | T | G | 16 | a0001c0001t0001g0168 a0001c0001t0001g0232 a0001c0001t0001g0245 others(13): Show |
16 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1944+916T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49189549 | |||||||
| chr13:49189648 | G | C | 1 | a0001c0001t0001g0288 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1944+1015G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49189648 | |||||||
| chr13:49189810 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1944+1177A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49189810 | |||||||
| chr13:49189812 | CA | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0078 |
3 | HG01070.hp1 HG01071.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1944+1182delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 49189812 | ||||||
| chr13:49189949 | C | T | 1 | a0002c0003t0001g0002 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1945-1066C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49189949 | |||||||
| chr13:49190047 | C | T | 2 | a0001c0001t0002g0169 a0001c0001t0002g0177 |
2 | HG00544.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1945-968C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190047 | |||||||
| chr13:49190063 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1945-952T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190063 | |||||||
| chr13:49190161 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1945-854C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190161 | |||||||
| chr13:49190175 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1945-840C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190175 | |||||||
| chr13:49190178 | G | A | 1 | a0001c0005t0001g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1945-837G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190178 | |||||||
| chr13:49190181 | C | T | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1945-834C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190181 | |||||||
| chr13:49190437 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1945-578A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190437 | |||||||
| chr13:49190443 | A | C | 1 | a0001c0001t0001g0266 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1945-572A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190443 | |||||||
| chr13:49190533 | A | C | 1 | a0001c0001t0001g0286 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1945-482A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190533 | |||||||
| chr13:49190672 | G | C | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1945-343G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190672 | |||||||
| chr13:49190915 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01074.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1945-100C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | chr13 | 49190915 | |||||||
| chr13:49190961 | C | CT | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.1945-53dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr13 | 49190961 | ||||||
| chr13:49191953 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | NA18612.hp2 NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2226+569C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49191953 | |||||||
| chr13:49192284 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2226+900T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49192284 | |||||||
| chr13:49192742 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2226+1358G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49192742 | |||||||
| chr13:49192786 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2226+1402T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49192786 | |||||||
| chr13:49192790 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2226+1406G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49192790 | |||||||
| chr13:49192792 | A | G | 1 | a0001c0002t0001g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2226+1408A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49192792 | |||||||
| chr13:49192819 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(1): Show |
4 | HG02818.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2226+1435T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49192819 | |||||||
| chr13:49192945 | A | G | 1 | a0001c0001t0007g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2226+1561A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49192945 | |||||||
| chr13:49193003 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2226+1619A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49193003 | |||||||
| chr13:49193662 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2226+2278G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49193662 | |||||||
| chr13:49193718 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2226+2334G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49193718 | |||||||
| chr13:49193733 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(270): Show |
273 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.2226+2349G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49193733 | |||||||
| chr13:49194016 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2226+2632T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49194016 | |||||||
| chr13:49194358 | A | G | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2227-2519A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49194358 | |||||||
| chr13:49194449 | T | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2227-2428T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49194449 | |||||||
| chr13:49194450 | G | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2227-2427G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49194450 | |||||||
| chr13:49194457 | A | G | 16 | a0001c0001t0001g0168 a0001c0001t0001g0232 a0001c0001t0001g0245 others(13): Show |
16 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.2227-2420A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49194457 | |||||||
| chr13:49194840 | A | G | 126 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0162 others(123): Show |
126 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2227-2037A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49194840 | |||||||
| chr13:49194855 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2227-2022G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49194855 | |||||||
| chr13:49194969 | T | G | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2227-1908T>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49194969 | |||||||
| chr13:49195071 | A | G | 4 | a0001c0001t0001g0186 a0001c0001t0001g0224 a0001c0001t0003g0183 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2227-1806A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49195071 | |||||||
| chr13:49195079 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2227-1798G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49195079 | |||||||
| chr13:49195173 | A | G | 120 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
120 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2227-1704A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49195173 | |||||||
| chr13:49195311 | C | T | 2 | a0001c0005t0001g0155 a0001c0005t0001g0156 |
2 | HG00741.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2227-1566C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49195311 | |||||||
| chr13:49195796 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2227-1081C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49195796 | |||||||
| chr13:49195953 | A | G | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02698.hp1 HG03688.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.2227-924A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49195953 | |||||||
| chr13:49196080 | C | CA | 113 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(110): Show |
113 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.2227-772dupA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr13 | 49196080 | ||||||
| chr13:49196080 | C | CAA | 14 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 others(11): Show |
14 | HG00741.hp2 HG01884.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.2227-773_2227-772d others(4): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr13 | 49196080 | ||||||
| chr13:49196080 | CA | C | 7 | a0001c0001t0001g0154 a0001c0001t0001g0184 a0001c0001t0001g0206 others(4): Show |
7 | HG01167.hp1 HG02135.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2227-772delA | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr13 | 49196080 | ||||||
| chr13:49196080 | CAAAAAAA | C | 14 | a0001c0001t0001g0185 a0001c0001t0001g0190 a0001c0001t0001g0195 others(11): Show |
14 | HG01433.hp2 HG01928.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.2227-778_2227-772d others(9): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr13 | 49196080 | ||||||
| chr13:49196080 | CAAAAAAA others(4): Show |
C | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
9 | HG01891.hp1 HG02698.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.2227-782_2227-772d others(13): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr13 | 49196080 | ||||||
| chr13:49196124 | A | G | 3 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0175 |
3 | HG00609.hp1 NA18942.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.2227-753A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49196124 | |||||||
| chr13:49196224 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2227-653T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49196224 | |||||||
| chr13:49196271 | A | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2227-606A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49196271 | |||||||
| chr13:49196346 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.2227-531G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49196346 | |||||||
| chr13:49196495 | TTAAAAAA others(7): Show |
T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0044 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.2227-378_2227-365d others(16): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr13 | 49196495 | ||||||
| chr13:49196643 | A | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2227-234A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49196643 | |||||||
| chr13:49196739 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2227-138C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49196739 | |||||||
| chr13:49196862 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02818.hp2 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2227-15C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 19/25 | chr13 | 49196862 | |||||||
| chr13:49197429 | C | CATTTCAT others(63): Show |
4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG01433.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2341-290_2341-221d others(72): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr13 | 49197429 | ||||||
| chr13:49197489 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2341-236G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 20/25 | chr13 | 49197489 | |||||||
| chr13:49197698 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2341-27G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 20/25 | chr13 | 49197698 | |||||||
| chr13:49198338 | CT | C | 15 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(12): Show |
15 | NA18948.hp2 NA18967.hp1 NA18969.hp1 others(12): Show |
intron_variant | MODIFIER | c.2775-17delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr13 | 49198338 | ||||||
| chr13:49198706 | C | T | 2 | a0001c0001t0001g0192 a0004c0007t0001g0191 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2987+132C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49198706 | |||||||
| chr13:49199085 | A | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2987+511A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49199085 | |||||||
| chr13:49199147 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02818.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2987+573A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49199147 | |||||||
| chr13:49199234 | T | C | 1 | a0001c0002t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2987+660T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49199234 | |||||||
| chr13:49199277 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | NA18612.hp2 NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2987+703T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49199277 | |||||||
| chr13:49199328 | A | AT | 20 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0105 others(17): Show |
20 | HG00597.hp2 HG00733.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.2987+774dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 49199328 | ||||||
| chr13:49199328 | AT | A | 34 | a0001c0001t0001g0044 a0001c0001t0001g0122 a0001c0001t0001g0127 others(31): Show |
34 | HG00741.hp2 HG01074.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.2987+774delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 49199328 | ||||||
| chr13:49199397 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2987+823G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49199397 | |||||||
| chr13:49199488 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2987+914C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49199488 | |||||||
| chr13:49199657 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2987+1083C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49199657 | |||||||
| chr13:49199667 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2987+1093C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49199667 | |||||||
| chr13:49199778 | G | C | 1 | a0001c0002t0001g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2987+1204G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49199778 | |||||||
| chr13:49199990 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0239 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2987+1416A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49199990 | |||||||
| chr13:49200054 | C | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2987+1480C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49200054 | |||||||
| chr13:49200193 | C | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(285): Show |
288 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.2988-1607C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49200193 | |||||||
| chr13:49200227 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2988-1573A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49200227 | |||||||
| chr13:49200249 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2988-1551A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49200249 | |||||||
| chr13:49200335 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2988-1465A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49200335 | |||||||
| chr13:49200417 | C | T | 115 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0162 others(112): Show |
115 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.2988-1383C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49200417 | |||||||
| chr13:49200425 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2988-1375C>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49200425 | |||||||
| chr13:49200698 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2988-1102G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49200698 | |||||||
| chr13:49200943 | A | AT | 9 | a0001c0002t0001g0057 a0001c0002t0001g0086 a0001c0002t0001g0087 others(6): Show |
9 | HG01496.hp2 HG03490.hp1 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.2988-848dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 49200943 | ||||||
| chr13:49201329 | C | CT | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2988-465dupT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr13 | 49201329 | ||||||
| chr13:49201624 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2988-176T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 23/25 | chr13 | 49201624 | |||||||
| chr13:49202171 | G | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3154+205G>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/25 | chr13 | 49202171 | |||||||
| chr13:49202183 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3154+217G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/25 | chr13 | 49202183 | |||||||
| chr13:49202204 | G | T | 66 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(63): Show |
66 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.3154+238G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/25 | chr13 | 49202204 | |||||||
| chr13:49202408 | A | G | 1 | a0001c0002t0001g0057 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3154+442A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/25 | chr13 | 49202408 | |||||||
| chr13:49202440 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3154+474A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/25 | chr13 | 49202440 | |||||||
| chr13:49202532 | A | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3154+566A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/25 | chr13 | 49202532 | |||||||
| chr13:49202682 | G | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3155-475G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/25 | chr13 | 49202682 | |||||||
| chr13:49202931 | A | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3155-226A>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/25 | chr13 | 49202931 | |||||||
| chr13:49203119 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3155-38C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 24/25 | chr13 | 49203119 | |||||||
| chr13:49203389 | T | C | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3282+105T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49203389 | |||||||
| chr13:49203865 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3282+581G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49203865 | |||||||
| chr13:49203987 | G | A | 6 | a0002c0003t0001g0002 a0002c0003t0001g0003 a0002c0003t0001g0004 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3282+703G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49203987 | |||||||
| chr13:49203992 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3282+708C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49203992 | |||||||
| chr13:49204700 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3282+1416G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49204700 | |||||||
| chr13:49204764 | GT | G | 117 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.3282+1484delT | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr13 | 49204764 | ||||||
| chr13:49205241 | C | G | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3283-1840C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49205241 | |||||||
| chr13:49205494 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3283-1587T>C | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49205494 | |||||||
| chr13:49205682 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3283-1399A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49205682 | |||||||
| chr13:49205921 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3283-1160G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49205921 | |||||||
| chr13:49206066 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.3283-1015A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49206066 | |||||||
| chr13:49206097 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3283-984G>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49206097 | |||||||
| chr13:49206337 | T | TCTTAA | 156 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0025 others(153): Show |
156 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.3283-740_3283-739i others(7): Show |
FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr13 | 49206337 | ||||||
| chr13:49206341 | A | T | 115 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(112): Show |
115 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.3283-740A>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49206341 | |||||||
| chr13:49206388 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3283-693A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49206388 | |||||||
| chr13:49206405 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3283-676C>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49206405 | |||||||
| chr13:49206423 | C | T | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3283-658C>T | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49206423 | |||||||
| chr13:49206499 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3283-582G>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49206499 | |||||||
| chr13:49206771 | T | A | 1 | a0001c0010t0004g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3283-310T>A | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49206771 | |||||||
| chr13:49206948 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3283-133A>G | FNDC3A | ENSG00000102531.16 | transcript | ENST00000492622.6 | protein_coding | 25/25 | chr13 | 49206948 |