Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 122786 |
| ensemblid | ENSG00000139926.16 |
| hgncid | 19839 |
| symbol | FRMD6 |
| name | FERM domain containing 6 |
| refseq_nuc | NM_001267046.2 |
| refseq_prot | NP_001253975.1 |
| ensembl_nuc | ENST00000344768.10 |
| ensembl_prot | ENSP00000343899.6 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 51651910 |
| end | 51730727 |
| strand | + |
| ver | v1.2 |
| region | chr14:51651910-51730727 |
| region5000 | chr14:51646910-51735727 |
| regionname0 | FRMD6_chr14_51651910_51730727 |
| regionname5000 | FRMD6_chr14_51646910_51735727 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 622 | 385 | 86 | 70 | 179 | 16 | 32 | 139 | FRMD6_chr14_51646910_51735727 | FRMD6 | MNKLN others(617): Show |
chr14 | 51646910 | 51735727 |
| a0002 | 0/0 | 622 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | MNKLN others(617): Show |
chr14 | 51646910 | 51735727 |
| a0003 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | MNKLN others(617): Show |
chr14 | 51646910 | 51735727 |
| a0004 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | MNKLN others(617): Show |
chr14 | 51646910 | 51735727 |
| a0005 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | MNKLN others(617): Show |
chr14 | 51646910 | 51735727 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1866 | 124 | 32 | 16 | 62 | 6 | 8 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0002 | 1/0 | 1866 | 111 | 22 | 29 | 41 | 4 | 14 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0003 | 0/1 | 1866 | 97 | 12 | 19 | 54 | 4 | 7 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0004 | 0/0 | 1866 | 21 | 9 | 4 | 4 | 1 | 3 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0005 | 0/0 | 1866 | 14 | 0 | 0 | 14 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0006 | 0/0 | 1866 | 10 | 8 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0007 | 0/0 | 1866 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0009 | 0/0 | 1866 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0011 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0013 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0014 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0001c0015 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0002c0008 | 0/0 | 1866 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0003c0010 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0004c0016 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 | ||
| a0005c0012 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | ATGAA others(1861): Show |
chr14 | 51646910 | 51735727 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4800 | 5 | 3 | 0 | 1 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0002 | 0/0 | 4801 | 103 | 20 | 12 | 58 | 6 | 7 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0006 | 0/0 | 4801 | 3 | 2 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0007 | 0/0 | 4801 | 3 | 0 | 3 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0010 | 0/0 | 4801 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0011 | 0/0 | 4801 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0018 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0019 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0020 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0021 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0023 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0001t0024 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0002t0001 | 1/0 | 4800 | 96 | 21 | 22 | 37 | 3 | 12 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0002t0002 | 0/0 | 4801 | 3 | 0 | 1 | 1 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0002t0004 | 0/0 | 4800 | 5 | 0 | 4 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0002t0008 | 0/0 | 4800 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0002t0013 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0002t0014 | 0/0 | 4800 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0002t0015 | 0/0 | 4800 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0002t0017 | 0/0 | 4800 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0003t0001 | 0/1 | 4800 | 95 | 12 | 17 | 54 | 4 | 7 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0003t0002 | 0/0 | 4801 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0001c0004t0001 | 0/0 | 4800 | 15 | 7 | 4 | 0 | 1 | 3 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0004t0005 | 0/0 | 4800 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0004t0012 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0004t0016 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0005t0001 | 0/0 | 4800 | 14 | 0 | 0 | 14 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0006t0003 | 0/0 | 4800 | 9 | 8 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0006t0022 | 0/0 | 4800 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0007t0001 | 0/0 | 4800 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0009t0001 | 0/0 | 4800 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0011t0001 | 0/0 | 4800 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0013t0001 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0014t0001 | 0/0 | 4800 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0001c0015t0001 | 0/0 | 4800 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0002c0008t0009 | 0/0 | 4800 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0003c0010t0001 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4795): Show |
chr14 | 51646910 | 51735727 |
| a0004c0016t0002 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| a0005c0012t0002 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | GAGGA others(4796): Show |
chr14 | 51646910 | 51735727 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0006g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0010g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0018g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0019g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0020g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0021g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0023g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0001t0024g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0003 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0004g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0008g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0014g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0015g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0002t0017g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0005 | 0/0 | 5 | 2 | 1 | 1 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0294 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0012g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0004t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0005t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0005t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0005t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0005t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0005t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0005t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0006t0003g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0006t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0006t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0006t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0006t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0006t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0006t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0006t0022g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0007t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0007t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0009t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0011t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0013t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0014t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0001c0015t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0002c0008t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0002c0008t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0003c0010t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0004c0016t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| a0005c0012t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0174 | EUR | GBR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | GBR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0303 | EUR | GBR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | GBR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0070 | EUR | FIN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00280 | hp2 | a0001 | c0002 | t0004 | g0242 | EUR | FIN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0302 | EUR | FIN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00323 | hp2 | a0001 | c0015 | t0001 | g0237 | EUR | FIN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0269 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0253 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0050 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00673 | hp2 | a0001 | c0014 | t0001 | g0008 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0230 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0139 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0259 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01069 | hp2 | a0001 | c0002 | t0004 | g0042 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0019 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0019 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0042 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01074 | hp1 | a0001 | c0002 | t0004 | g0233 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0068 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0157 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0256 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0067 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0263 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0276 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0257 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0292 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0217 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01192 | hp2 | a0001 | c0002 | t0004 | g0218 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01243 | hp1 | a0001 | c0002 | t0017 | g0209 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0023 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0249 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0021 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0119 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01358 | hp1 | a0001 | c0006 | t0003 | g0165 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0222 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0225 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01433 | hp1 | a0001 | c0006 | t0022 | g0161 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01496 | hp1 | a0001 | c0002 | t0015 | g0235 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0262 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0201 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0053 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0064 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0019 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0274 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0261 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0290 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0271 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02074 | hp1 | a0001 | c0005 | t0001 | g0246 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0277 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02083 | hp2 | a0001 | c0004 | t0005 | g0184 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0266 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02145 | hp2 | a0001 | c0006 | t0003 | g0011 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | CDX | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | CDX | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02165 | hp1 | a0001 | c0001 | t0020 | g0129 | EAS | CDX | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CDX | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02258 | hp2 | a0002 | c0008 | t0009 | g0281 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02280 | hp2 | a0001 | c0006 | t0003 | g0011 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0264 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02523 | hp2 | a0001 | c0005 | t0001 | g0288 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02572 | hp2 | a0002 | c0008 | t0009 | g0074 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0208 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02630 | hp1 | a0001 | c0007 | t0001 | g0057 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0069 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02723 | hp1 | a0001 | c0013 | t0001 | g0197 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0142 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0232 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02818 | hp2 | a0001 | c0004 | t0016 | g0072 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02895 | hp2 | a0001 | c0004 | t0001 | g0039 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0130 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0039 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0131 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02922 | hp1 | a0001 | c0001 | t0021 | g0214 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02922 | hp2 | a0001 | c0002 | t0013 | g0056 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02970 | hp2 | a0001 | c0006 | t0003 | g0075 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02976 | hp1 | a0001 | c0006 | t0003 | g0150 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0279 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0141 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03098 | hp2 | a0001 | c0006 | t0003 | g0152 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0038 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03139 | hp1 | a0003 | c0010 | t0001 | g0073 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0204 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03195 | hp2 | a0001 | c0006 | t0003 | g0151 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03209 | hp1 | a0001 | c0004 | t0012 | g0180 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03239 | hp1 | a0001 | c0004 | t0001 | g0071 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0049 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0096 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03486 | hp1 | a0001 | c0006 | t0003 | g0181 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03486 | hp2 | a0001 | c0001 | t0024 | g0123 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0016 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03491 | hp1 | a0001 | c0002 | t0014 | g0238 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0016 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03516 | hp2 | a0001 | c0006 | t0003 | g0011 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03540 | hp2 | a0001 | c0007 | t0001 | g0099 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0060 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0049 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0098 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03834 | hp1 | a0001 | c0004 | t0001 | g0023 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0194 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0200 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0299 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0258 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0240 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0097 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | CHB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | CHB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | CHB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18906 | hp1 | a0001 | c0001 | t0019 | g0101 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0287 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18944 | hp1 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18946 | hp2 | a0001 | c0009 | t0001 | g0024 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0247 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18950 | hp1 | a0001 | c0005 | t0001 | g0289 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18952 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18957 | hp2 | a0001 | c0002 | t0008 | g0018 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18961 | hp2 | a0001 | c0002 | t0008 | g0018 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0252 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18962 | hp2 | a0001 | c0001 | t0010 | g0109 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18964 | hp2 | a0001 | c0005 | t0001 | g0048 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0270 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18968 | hp1 | a0001 | c0011 | t0001 | g0251 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18968 | hp2 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18969 | hp1 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18971 | hp1 | a0001 | c0005 | t0001 | g0125 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0243 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0250 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0245 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0297 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18983 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18988 | hp1 | a0001 | c0003 | t0001 | g0273 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18990 | hp2 | a0001 | c0003 | t0001 | g0254 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18991 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0272 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18994 | hp2 | a0001 | c0004 | t0005 | g0183 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0268 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19003 | hp1 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19005 | hp2 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19006 | hp1 | a0001 | c0003 | t0001 | g0265 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19009 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0283 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19010 | hp2 | a0001 | c0009 | t0001 | g0024 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0278 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0203 | AFR | LWK | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0192 | AFR | LWK | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19055 | hp1 | a0001 | c0004 | t0005 | g0282 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0255 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19063 | hp2 | a0001 | c0002 | t0008 | g0018 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19066 | hp1 | a0004 | c0016 | t0002 | g0104 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19067 | hp2 | a0001 | c0003 | t0001 | g0267 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0298 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19078 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19079 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19081 | hp2 | a0001 | c0005 | t0001 | g0048 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19082 | hp2 | a0001 | c0004 | t0005 | g0188 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19087 | hp1 | a0001 | c0005 | t0001 | g0296 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19240 | hp1 | a0005 | c0012 | t0002 | g0206 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | ASW | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ASW | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0015 | EUR | TSI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0173 | EUR | TSI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0224 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0189 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02559 | hp1 | a0001 | c0001 | t0018 | g0030 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03471 | hp1 | a0001 | c0001 | t0023 | g0062 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | USA | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | USA | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | USA | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | USA | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | LWK | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | LWK | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0294 | REF | REF | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0140 | REF | REF | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:51689860 | C | A | 1 | a0003 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.24C>A | p.Asn8Lys | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/14 | 257/4800 | 24/1869 | 8/622 | chr14 | 51689860 | |||
| chr14:51689930 | A | G | 1 | a0004 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.94A>G | p.Ile32Val | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/14 | 327/4800 | 94/1869 | 32/622 | chr14 | 51689930 | |||
| chr14:51720216 | G | A | 1 | a0005 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1186G>A | p.Gly396Ser | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1419/4800 | 1186/1869 | 396/622 | chr14 | 51720216 | |||
| chr14:51727853 | A | T | 1 | a0002 | 2 | HG02258.hp2 HG02572.hp2 |
missense_variant | MODERATE | c.1693A>T | p.Thr565Ser | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1926/4800 | 1693/1869 | 565/622 | chr14 | 51727853 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:51698198 | G | A | 1 | a0001c0007 | 2 | HG02630.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.156G>A | p.Lys52Lys | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/14 | 389/4800 | 156/1869 | 52/622 | chr14 | 51698198 | |||
| chr14:51708158 | C | T | 1 | a0001c0005 | 14 | HG02074.hp1 HG02523.hp2 NA18944.hp1 others(11): Show |
synonymous_variant | LOW | c.639C>T | p.Ser213Ser | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/14 | 872/4800 | 639/1869 | 213/622 | chr14 | 51708158 | |||
| chr14:51715363 | T | A | 11 | a0001c0001 a0001c0003 a0001c0004 others(8): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
synonymous_variant | LOW | c.888T>A | p.Ser296Ser | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/14 | 1121/4800 | 888/1869 | 296/622 | chr14 | 51715363 | |||
| chr14:51715390 | G | A | 1 | a0001c0011 | 1 | NA18968.hp1 | synonymous_variant | LOW | c.915G>A | p.Gly305Gly | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/14 | 1148/4800 | 915/1869 | 305/622 | chr14 | 51715390 | |||
| chr14:51720077 | T | C | 1 | a0001c0006 | 10 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
synonymous_variant | LOW | c.1047T>C | p.Ser349Ser | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1280/4800 | 1047/1869 | 349/622 | chr14 | 51720077 | |||
| chr14:51720092 | C | T | 1 | a0001c0013 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1062C>T | p.Asn354Asn | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1295/4800 | 1062/1869 | 354/622 | chr14 | 51720092 | |||
| chr14:51720248 | G | A | 5 | a0001c0003 a0001c0007 a0001c0009 others(2): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
synonymous_variant | LOW | c.1218G>A | p.Thr406Thr | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1451/4800 | 1218/1869 | 406/622 | chr14 | 51720248 | |||
| chr14:51720254 | A | G | 4 | a0001c0001 a0001c0015 a0004c0016 others(1): Show |
127 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(124): Show |
synonymous_variant | LOW | c.1224A>G | p.Pro408Pro | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1457/4800 | 1224/1869 | 408/622 | chr14 | 51720254 | |||
| chr14:51720323 | C | T | 1 | a0001c0014 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.1293C>T | p.Gly431Gly | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1526/4800 | 1293/1869 | 431/622 | chr14 | 51720323 | |||
| chr14:51722052 | C | T | 1 | a0002c0008 | 2 | HG02258.hp2 HG02572.hp2 |
synonymous_variant | LOW | c.1464C>T | p.Leu488Leu | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/14 | 1697/4800 | 1464/1869 | 488/622 | chr14 | 51722052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:51651917 | G | A | 1 | a0001c0002t0004 | 5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-226G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/14 | 37920 | chr14 | 51651917 | ||||||
| chr14:51651935 | G | T | 1 | a0001c0001t0011 | 2 | HG02896.hp2 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-208G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/14 | 37902 | chr14 | 51651935 | ||||||
| chr14:51728037 | C | G | 1 | a0001c0001t0024 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 8 | chr14 | 51728037 | ||||||
| chr14:51728080 | C | T | 1 | a0001c0001t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 51 | chr14 | 51728080 | ||||||
| chr14:51728115 | A | G | 1 | a0001c0002t0008 | 3 | NA18957.hp2 NA18961.hp2 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*86A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 86 | chr14 | 51728115 | ||||||
| chr14:51728232 | G | T | 2 | a0001c0006t0003 a0001c0006t0022 |
10 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*203G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 203 | chr14 | 51728232 | ||||||
| chr14:51728371 | A | AT | 15 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(12): Show |
126 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*349dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 350 | INFO_REALIGN_3_PRIME | chr14 | 51728371 | |||||
| chr14:51728572 | G | A | 16 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(13): Show |
127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*543G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 543 | chr14 | 51728572 | ||||||
| chr14:51728602 | A | G | 16 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(13): Show |
127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*573A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 573 | chr14 | 51728602 | ||||||
| chr14:51728827 | C | T | 1 | a0001c0002t0017 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*798C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 798 | chr14 | 51728827 | ||||||
| chr14:51728915 | A | G | 1 | a0002c0008t0009 | 2 | HG02258.hp2 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*886A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 886 | chr14 | 51728915 | ||||||
| chr14:51729138 | T | C | 1 | a0001c0001t0018 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1109T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1109 | chr14 | 51729138 | ||||||
| chr14:51729397 | A | G | 1 | a0001c0001t0007 | 3 | HG00733.hp2 HG01109.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1368A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1368 | chr14 | 51729397 | ||||||
| chr14:51729450 | A | C | 1 | a0001c0001t0021 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1421 | chr14 | 51729450 | ||||||
| chr14:51729565 | C | T | 1 | a0001c0004t0016 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1536C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1536 | chr14 | 51729565 | ||||||
| chr14:51729599 | A | C | 1 | a0001c0004t0005 | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1570A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1570 | chr14 | 51729599 | ||||||
| chr14:51729616 | A | G | 1 | a0001c0006t0022 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1587A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1587 | chr14 | 51729616 | ||||||
| chr14:51729780 | C | T | 1 | a0001c0001t0024 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1751C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1751 | chr14 | 51729780 | ||||||
| chr14:51729787 | G | A | 15 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(12): Show |
126 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1758G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1758 | chr14 | 51729787 | ||||||
| chr14:51729963 | A | G | 2 | a0001c0001t0006 a0001c0001t0023 |
4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1934A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1934 | chr14 | 51729963 | ||||||
| chr14:51730095 | T | C | 1 | a0001c0001t0019 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2066T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2066 | chr14 | 51730095 | ||||||
| chr14:51730123 | A | C | 1 | a0001c0001t0024 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2094A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2094 | chr14 | 51730123 | ||||||
| chr14:51730224 | T | A | 1 | a0001c0001t0010 | 2 | NA18962.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2195T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2195 | chr14 | 51730224 | ||||||
| chr14:51730237 | G | A | 1 | a0001c0002t0013 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2208G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2208 | chr14 | 51730237 | ||||||
| chr14:51730365 | A | T | 1 | a0001c0002t0015 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2336A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2336 | chr14 | 51730365 | ||||||
| chr14:51730396 | G | T | 1 | a0001c0001t0020 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2367G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2367 | chr14 | 51730396 | ||||||
| chr14:51730492 | A | G | 1 | a0001c0002t0014 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2463A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2463 | chr14 | 51730492 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:51652017 | T | C | 1 | a0001c0004t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-147+21T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652017 | |||||||
| chr14:51652036 | C | T | 1 | a0001c0001t0002g0304 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-147+40C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652036 | |||||||
| chr14:51652073 | T | C | 1 | a0001c0001t0002g0051 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-147+77T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652073 | |||||||
| chr14:51652082 | C | T | 4 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0003t0001g0302 others(1): Show |
4 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+86C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652082 | |||||||
| chr14:51652129 | C | G | 69 | a0001c0001t0002g0248 a0001c0001t0002g0275 a0001c0001t0002g0284 others(66): Show |
93 | HG00438.hp1 HG00544.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.-147+133C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652129 | |||||||
| chr14:51652250 | T | C | 28 | a0001c0001t0002g0022 a0001c0001t0002g0052 a0001c0001t0002g0053 others(25): Show |
31 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-147+254T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652250 | |||||||
| chr14:51652262 | G | T | 1 | a0001c0002t0004g0242 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-147+266G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652262 | |||||||
| chr14:51652278 | A | G | 1 | a0001c0002t0001g0241 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-147+282A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652278 | |||||||
| chr14:51652317 | G | C | 1 | a0001c0002t0001g0076 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-147+321G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652317 | |||||||
| chr14:51652318 | G | T | 32 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0226 others(29): Show |
43 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-147+322G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652318 | |||||||
| chr14:51652389 | C | G | 187 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(184): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-147+393C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652389 | |||||||
| chr14:51652449 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-147+453C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652449 | |||||||
| chr14:51652507 | G | A | 19 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(16): Show |
23 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-147+511G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652507 | |||||||
| chr14:51652516 | G | T | 1 | a0001c0004t0001g0039 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-147+520G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652516 | |||||||
| chr14:51652518 | C | G | 19 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(16): Show |
23 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-147+522C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652518 | |||||||
| chr14:51652547 | C | G | 53 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(50): Show |
69 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-147+551C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652547 | |||||||
| chr14:51652602 | A | G | 1 | a0001c0013t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-147+606A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652602 | |||||||
| chr14:51652698 | A | G | 3 | a0001c0002t0001g0037 a0001c0002t0001g0195 a0001c0002t0001g0196 |
4 | HG02615.hp1 HG02809.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147+702A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652698 | |||||||
| chr14:51652821 | T | C | 4 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(1): Show |
4 | HG00738.hp1 HG01256.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147+825T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652821 | |||||||
| chr14:51653065 | A | G | 1 | a0001c0003t0001g0299 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-147+1069A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653065 | |||||||
| chr14:51653069 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-147+1073C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653069 | |||||||
| chr14:51653190 | T | G | 1 | a0001c0002t0001g0077 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-147+1194T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653190 | |||||||
| chr14:51653205 | G | GT | 58 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(55): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-147+1210dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51653205 | ||||||
| chr14:51653238 | G | A | 10 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(7): Show |
10 | HG00738.hp1 HG01256.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.-147+1242G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653238 | |||||||
| chr14:51653253 | G | T | 12 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(9): Show |
12 | HG00738.hp1 HG01256.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.-147+1257G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653253 | |||||||
| chr14:51653356 | A | G | 2 | a0001c0003t0001g0297 a0001c0003t0001g0298 |
2 | NA18981.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-147+1360A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653356 | |||||||
| chr14:51653437 | TG | T | 3 | a0001c0002t0001g0037 a0001c0002t0001g0195 a0001c0002t0001g0196 |
4 | HG02615.hp1 HG02809.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147+1445delG | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51653437 | ||||||
| chr14:51653527 | C | T | 1 | a0001c0006t0003g0165 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-147+1531C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653527 | |||||||
| chr14:51653546 | A | G | 187 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(184): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-147+1550A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653546 | |||||||
| chr14:51653546 | A | T | 1 | a0001c0006t0003g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-147+1550A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653546 | |||||||
| chr14:51653547 | T | G | 1 | a0001c0003t0001g0243 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-147+1551T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653547 | |||||||
| chr14:51653596 | T | A | 26 | a0001c0001t0002g0022 a0001c0001t0002g0052 a0001c0001t0002g0053 others(23): Show |
29 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-147+1600T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653596 | |||||||
| chr14:51653607 | A | T | 1 | a0001c0003t0001g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-147+1611A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653607 | |||||||
| chr14:51653748 | G | T | 11 | a0001c0001t0002g0022 a0001c0001t0002g0064 a0001c0001t0002g0065 others(8): Show |
13 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.-147+1752G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653748 | |||||||
| chr14:51653770 | A | G | 1 | a0001c0003t0001g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-147+1774A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653770 | |||||||
| chr14:51653778 | A | G | 1 | a0001c0003t0001g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-147+1782A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653778 | |||||||
| chr14:51653786 | C | T | 2 | a0001c0006t0003g0075 a0002c0008t0009g0074 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-147+1790C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653786 | |||||||
| chr14:51653844 | A | G | 3 | a0001c0001t0006g0021 a0001c0001t0006g0063 a0001c0001t0023g0062 |
4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+1848A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653844 | |||||||
| chr14:51653854 | G | T | 3 | a0001c0002t0001g0191 a0001c0003t0001g0192 a0001c0013t0001g0197 |
3 | HG02723.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-147+1858G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653854 | |||||||
| chr14:51654027 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-147+2031C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654027 | |||||||
| chr14:51654102 | G | A | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-147+2106G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654102 | |||||||
| chr14:51654104 | A | C | 1 | a0001c0002t0001g0240 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-147+2108A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654104 | |||||||
| chr14:51654303 | AT | A | 6 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(3): Show |
6 | HG00738.hp1 HG01256.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147+2309delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654303 | ||||||
| chr14:51654305 | T | G | 6 | a0001c0001t0002g0058 a0001c0002t0001g0061 a0001c0002t0013g0056 others(3): Show |
6 | HG02630.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147+2309T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654305 | |||||||
| chr14:51654305 | T | TG | 102 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0084 others(99): Show |
137 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.-147+2319dupG | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654305 | ||||||
| chr14:51654305 | T | TGG | 56 | a0001c0001t0001g0205 a0001c0001t0002g0014 a0001c0001t0002g0022 others(53): Show |
73 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-147+2318_-147+231 others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654305 | ||||||
| chr14:51654305 | T | TGGG | 19 | a0001c0001t0001g0198 a0001c0001t0002g0064 a0001c0001t0002g0199 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-147+2317_-147+231 others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654305 | ||||||
| chr14:51654389 | A | G | 4 | a0001c0002t0001g0077 a0001c0002t0001g0093 a0001c0002t0001g0094 others(1): Show |
5 | NA18946.hp2 NA18972.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147+2393A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654389 | |||||||
| chr14:51654505 | A | C | 2 | a0001c0001t0006g0021 a0001c0001t0006g0063 |
3 | HG01261.hp1 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-147+2509A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654505 | |||||||
| chr14:51654510 | C | G | 1 | a0001c0001t0023g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-147+2514C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654510 | |||||||
| chr14:51654580 | G | GT | 6 | a0001c0001t0002g0058 a0001c0002t0001g0015 a0001c0002t0001g0061 others(3): Show |
8 | HG01361.hp1 HG01433.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-147+2597dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654580 | ||||||
| chr14:51654580 | GT | G | 10 | a0001c0001t0006g0021 a0001c0001t0006g0063 a0001c0001t0023g0062 others(7): Show |
11 | HG01167.hp2 HG01257.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-147+2597delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654580 | ||||||
| chr14:51654682 | G | T | 1 | a0001c0001t0002g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-147+2686G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654682 | |||||||
| chr14:51654766 | T | C | 1 | a0001c0003t0001g0095 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-147+2770T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654766 | |||||||
| chr14:51655046 | TA | T | 42 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(39): Show |
47 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.-147+3066delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51655046 | ||||||
| chr14:51655086 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-147+3090C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655086 | |||||||
| chr14:51655370 | A | C | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-147+3374A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655370 | |||||||
| chr14:51655719 | G | A | 1 | a0001c0003t0001g0253 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-147+3723G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655719 | |||||||
| chr14:51655759 | C | T | 69 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(66): Show |
86 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-147+3763C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655759 | |||||||
| chr14:51655861 | G | A | 2 | a0001c0006t0003g0075 a0002c0008t0009g0074 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-147+3865G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655861 | |||||||
| chr14:51655901 | C | T | 57 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(54): Show |
74 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-147+3905C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655901 | |||||||
| chr14:51655914 | A | G | 1 | a0001c0002t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-147+3918A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655914 | |||||||
| chr14:51656096 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-147+4100A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656096 | |||||||
| chr14:51656182 | A | G | 1 | a0001c0002t0001g0164 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-147+4186A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656182 | |||||||
| chr14:51656221 | A | G | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-147+4225A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656221 | |||||||
| chr14:51656319 | T | A | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-147+4323T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656319 | |||||||
| chr14:51656352 | G | C | 187 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(184): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-147+4356G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656352 | |||||||
| chr14:51656355 | A | T | 69 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(66): Show |
86 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-147+4359A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656355 | |||||||
| chr14:51656369 | T | G | 2 | a0001c0006t0003g0075 a0002c0008t0009g0074 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-147+4373T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656369 | |||||||
| chr14:51656430 | C | T | 302 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(299): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-147+4434C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656430 | |||||||
| chr14:51656436 | C | T | 68 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(65): Show |
87 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-147+4440C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656436 | |||||||
| chr14:51656444 | C | T | 19 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(16): Show |
23 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-147+4448C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656444 | |||||||
| chr14:51656570 | C | T | 1 | a0001c0002t0001g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-147+4574C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656570 | |||||||
| chr14:51656664 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-147+4668G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656664 | |||||||
| chr14:51656696 | G | A | 2 | a0001c0006t0003g0075 a0002c0008t0009g0074 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-147+4700G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656696 | |||||||
| chr14:51656702 | G | A | 2 | a0001c0004t0001g0203 a0001c0004t0001g0204 |
2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-147+4706G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656702 | |||||||
| chr14:51656746 | G | A | 2 | a0001c0001t0006g0021 a0001c0001t0006g0063 |
3 | HG01261.hp1 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-147+4750G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656746 | |||||||
| chr14:51656753 | C | T | 1 | a0001c0003t0001g0244 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-147+4757C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656753 | |||||||
| chr14:51656928 | A | G | 1 | a0001c0002t0001g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-147+4932A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656928 | |||||||
| chr14:51656964 | A | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
8 | HG00673.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.-147+4968A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656964 | |||||||
| chr14:51657095 | TATA | T | 5 | a0001c0001t0002g0058 a0001c0002t0001g0061 a0001c0002t0013g0056 others(2): Show |
5 | HG02630.hp1 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147+5102_-147+510 others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51657095 | ||||||
| chr14:51657110 | C | T | 1 | a0001c0003t0001g0293 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-147+5114C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657110 | |||||||
| chr14:51657297 | G | A | 1 | a0001c0003t0001g0016 | 3 | HG00735.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-147+5301G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657297 | |||||||
| chr14:51657299 | G | A | 4 | a0001c0001t0002g0022 a0001c0001t0002g0064 a0001c0001t0002g0065 others(1): Show |
5 | HG00099.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147+5303G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657299 | |||||||
| chr14:51657349 | C | T | 1 | a0001c0003t0001g0298 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-147+5353C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657349 | |||||||
| chr14:51657390 | C | T | 8 | a0001c0003t0001g0049 a0001c0004t0001g0023 a0001c0004t0001g0050 others(5): Show |
10 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-147+5394C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657390 | |||||||
| chr14:51657522 | A | T | 1 | a0001c0002t0001g0213 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-147+5526A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657522 | |||||||
| chr14:51657533 | G | A | 1 | a0001c0013t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-147+5537G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657533 | |||||||
| chr14:51657554 | G | C | 116 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0022 others(113): Show |
151 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-147+5558G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657554 | |||||||
| chr14:51657653 | C | A | 1 | a0001c0003t0001g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-147+5657C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657653 | |||||||
| chr14:51657691 | G | C | 1 | a0001c0004t0001g0039 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-147+5695G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657691 | |||||||
| chr14:51657703 | A | G | 196 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(193): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.-147+5707A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657703 | |||||||
| chr14:51657704 | A | G | 1 | a0001c0003t0001g0283 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-147+5708A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657704 | |||||||
| chr14:51657716 | A | G | 1 | a0001c0002t0001g0143 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-147+5720A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657716 | |||||||
| chr14:51657790 | C | G | 1 | a0001c0006t0022g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-147+5794C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657790 | |||||||
| chr14:51657827 | GA | G | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+5832delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657827 | |||||||
| chr14:51658134 | G | A | 1 | a0001c0004t0001g0067 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-147+6138G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658134 | |||||||
| chr14:51658134 | G | C | 1 | a0001c0004t0001g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-147+6138G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658134 | |||||||
| chr14:51658154 | A | G | 9 | a0001c0003t0001g0059 a0001c0006t0003g0011 a0001c0006t0003g0075 others(6): Show |
11 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-147+6158A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658154 | |||||||
| chr14:51658245 | A | G | 29 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0003t0001g0192 others(26): Show |
33 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.-147+6249A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658245 | |||||||
| chr14:51658326 | T | TTC | 51 | a0001c0001t0007g0157 a0001c0002t0001g0003 a0001c0002t0001g0015 others(48): Show |
62 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-147+6331_-147+633 others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51658326 | ||||||
| chr14:51658328 | T | C | 301 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(298): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.-147+6332T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658328 | |||||||
| chr14:51658328 | T | TTC | 3 | a0001c0002t0001g0202 a0001c0002t0001g0212 a0001c0002t0001g0213 |
3 | HG01884.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-147+6345_-147+634 others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51658328 | ||||||
| chr14:51658375 | G | T | 1 | a0001c0001t0002g0138 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-147+6379G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658375 | |||||||
| chr14:51658406 | CCTCTTGA others(4): Show |
C | 7 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(4): Show |
8 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-147+6417_-147+642 others(15): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51658406 | ||||||
| chr14:51658475 | C | T | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+6479C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658475 | |||||||
| chr14:51658522 | A | G | 1 | a0001c0003t0001g0192 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-147+6526A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658522 | |||||||
| chr14:51658613 | G | A | 9 | a0001c0003t0001g0059 a0001c0006t0003g0011 a0001c0006t0003g0075 others(6): Show |
11 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-147+6617G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658613 | |||||||
| chr14:51658664 | G | A | 19 | a0001c0001t0002g0176 a0001c0003t0001g0192 a0001c0004t0001g0023 others(16): Show |
20 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-147+6668G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658664 | |||||||
| chr14:51658664 | G | T | 1 | a0001c0001t0002g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-147+6668G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658664 | |||||||
| chr14:51658789 | A | C | 217 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(214): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-147+6793A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658789 | |||||||
| chr14:51658880 | A | G | 2 | a0001c0001t0002g0176 a0001c0004t0012g0180 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-147+6884A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658880 | |||||||
| chr14:51658930 | G | A | 1 | a0001c0003t0001g0249 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-147+6934G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658930 | |||||||
| chr14:51658965 | A | G | 29 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0003t0001g0192 others(26): Show |
33 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.-147+6969A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658965 | |||||||
| chr14:51659181 | C | T | 1 | a0003c0010t0001g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-147+7185C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659181 | |||||||
| chr14:51659635 | A | G | 6 | a0001c0002t0001g0033 a0001c0002t0001g0177 a0001c0002t0001g0178 others(3): Show |
7 | HG01516.hp2 HG01884.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-147+7639A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659635 | |||||||
| chr14:51659679 | C | T | 1 | a0001c0003t0001g0278 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-147+7683C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659679 | |||||||
| chr14:51659802 | A | T | 53 | a0001c0001t0007g0157 a0001c0002t0001g0003 a0001c0002t0001g0015 others(50): Show |
64 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-147+7806A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659802 | |||||||
| chr14:51659819 | A | G | 1 | a0001c0003t0001g0192 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-147+7823A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659819 | |||||||
| chr14:51659866 | T | C | 7 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(4): Show |
9 | HG01074.hp2 HG01099.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-147+7870T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659866 | |||||||
| chr14:51659904 | A | T | 9 | a0001c0003t0001g0059 a0001c0006t0003g0011 a0001c0006t0003g0075 others(6): Show |
11 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-147+7908A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659904 | |||||||
| chr14:51659978 | C | G | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-147+7982C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659978 | |||||||
| chr14:51659982 | T | C | 1 | a0001c0001t0006g0063 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-147+7986T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659982 | |||||||
| chr14:51660133 | C | T | 7 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(4): Show |
9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+8137C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660133 | |||||||
| chr14:51660329 | A | G | 9 | a0001c0003t0001g0059 a0001c0006t0003g0011 a0001c0006t0003g0075 others(6): Show |
11 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-147+8333A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660329 | |||||||
| chr14:51660341 | A | G | 217 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(214): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-147+8345A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660341 | |||||||
| chr14:51660373 | C | T | 2 | a0001c0001t0002g0065 a0001c0001t0002g0066 |
2 | NA18951.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-147+8377C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660373 | |||||||
| chr14:51660419 | C | A | 28 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0003t0001g0192 others(25): Show |
31 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-147+8423C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660419 | |||||||
| chr14:51660488 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-147+8492A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660488 | |||||||
| chr14:51660613 | G | GA | 123 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(120): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-147+8635dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51660613 | ||||||
| chr14:51660613 | G | GAA | 18 | a0001c0002t0001g0093 a0001c0003t0001g0025 a0001c0003t0001g0044 others(15): Show |
21 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-147+8634_-147+863 others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51660613 | ||||||
| chr14:51660613 | G | GAAA | 10 | a0001c0003t0001g0059 a0001c0003t0001g0078 a0001c0003t0001g0080 others(7): Show |
12 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-147+8633_-147+863 others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51660613 | ||||||
| chr14:51660613 | GA | G | 14 | a0001c0001t0002g0058 a0001c0001t0002g0147 a0001c0001t0002g0148 others(11): Show |
14 | HG01074.hp2 HG01099.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-147+8635delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51660613 | ||||||
| chr14:51660613 | GAAA | G | 52 | a0001c0001t0007g0157 a0001c0002t0001g0003 a0001c0002t0001g0015 others(49): Show |
63 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-147+8633_-147+863 others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51660613 | ||||||
| chr14:51660632 | T | C | 29 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0003t0001g0192 others(26): Show |
33 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.-147+8636T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660632 | |||||||
| chr14:51660746 | T | A | 2 | a0001c0003t0001g0059 a0003c0010t0001g0073 |
2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-147+8750T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660746 | |||||||
| chr14:51660786 | T | C | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+8790T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660786 | |||||||
| chr14:51660903 | G | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0127 a0001c0001t0002g0128 |
5 | NA18950.hp2 NA18966.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147+8907G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660903 | |||||||
| chr14:51661119 | A | G | 132 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(129): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-147+9123A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661119 | |||||||
| chr14:51661147 | G | A | 1 | a0001c0002t0001g0229 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-147+9151G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661147 | |||||||
| chr14:51661276 | G | A | 28 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0003t0001g0192 others(25): Show |
31 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-147+9280G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661276 | |||||||
| chr14:51661398 | G | A | 8 | a0001c0001t0002g0030 a0001c0001t0002g0051 a0001c0001t0002g0144 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-147+9402G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661398 | |||||||
| chr14:51661462 | A | G | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+9466A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661462 | |||||||
| chr14:51661483 | G | A | 1 | a0003c0010t0001g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-147+9487G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661483 | |||||||
| chr14:51661889 | C | T | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+9893C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661889 | |||||||
| chr14:51662057 | C | T | 2 | a0001c0002t0001g0201 a0001c0002t0001g0215 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-147+10061C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662057 | |||||||
| chr14:51662179 | T | C | 30 | a0001c0001t0002g0176 a0001c0002t0001g0194 a0001c0003t0001g0059 others(27): Show |
34 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-147+10183T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662179 | |||||||
| chr14:51662330 | G | A | 130 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(127): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.-147+10334G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662330 | |||||||
| chr14:51662787 | G | T | 21 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0003t0001g0192 others(18): Show |
22 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-147+10791G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662787 | |||||||
| chr14:51662953 | G | A | 2 | a0001c0003t0001g0302 a0001c0003t0001g0303 |
2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.-147+10957G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662953 | |||||||
| chr14:51662955 | G | A | 1 | a0001c0002t0001g0201 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-147+10959G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662955 | |||||||
| chr14:51663184 | C | A | 214 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(211): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.-147+11188C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663184 | |||||||
| chr14:51663410 | A | G | 22 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0003t0001g0192 others(19): Show |
24 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-147+11414A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663410 | |||||||
| chr14:51663412 | A | T | 1 | a0001c0002t0001g0211 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-147+11416A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663412 | |||||||
| chr14:51663452 | T | C | 7 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(4): Show |
9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+11456T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663452 | |||||||
| chr14:51663461 | A | C | 215 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(212): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-147+11465A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663461 | |||||||
| chr14:51663605 | G | T | 1 | a0001c0003t0001g0290 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-147+11609G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663605 | |||||||
| chr14:51663663 | G | C | 1 | a0001c0002t0001g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-147+11667G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663663 | |||||||
| chr14:51663857 | G | A | 3 | a0001c0003t0001g0017 a0001c0003t0001g0256 a0001c0003t0001g0257 |
5 | HG01081.hp2 HG01106.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-147+11861G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663857 | |||||||
| chr14:51663886 | G | A | 13 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(10): Show |
14 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-147+11890G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663886 | |||||||
| chr14:51664252 | G | A | 4 | a0001c0002t0001g0034 a0001c0002t0001g0171 a0001c0002t0001g0172 others(1): Show |
5 | HG00741.hp2 HG01070.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-147+12256G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664252 | |||||||
| chr14:51664310 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-147+12314G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664310 | |||||||
| chr14:51664375 | A | G | 1 | a0001c0002t0001g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-147+12379A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664375 | |||||||
| chr14:51664396 | C | T | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+12400C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664396 | |||||||
| chr14:51664422 | A | C | 7 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(4): Show |
9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+12426A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664422 | |||||||
| chr14:51664481 | C | T | 1 | a0001c0004t0001g0039 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-147+12485C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664481 | |||||||
| chr14:51664854 | CAGTTAGT others(3): Show |
C | 1 | a0001c0002t0001g0085 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-147+12860_-147+12 others(16): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51664854 | ||||||
| chr14:51664866 | A | C | 1 | a0001c0002t0001g0085 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-147+12870A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664866 | |||||||
| chr14:51665025 | G | T | 21 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0003t0001g0192 others(18): Show |
22 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-147+13029G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665025 | |||||||
| chr14:51665038 | G | A | 52 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0031 others(49): Show |
64 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-147+13042G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665038 | |||||||
| chr14:51665215 | G | T | 7 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(4): Show |
9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+13219G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665215 | |||||||
| chr14:51665218 | G | A | 1 | a0001c0004t0001g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-147+13222G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665218 | |||||||
| chr14:51665237 | C | A | 1 | a0003c0010t0001g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-147+13241C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665237 | |||||||
| chr14:51665238 | C | T | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+13242C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665238 | |||||||
| chr14:51665279 | C | A | 2 | a0001c0002t0004g0042 a0001c0002t0004g0218 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-147+13283C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665279 | |||||||
| chr14:51665287 | G | T | 1 | a0001c0013t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-147+13291G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665287 | |||||||
| chr14:51665483 | G | A | 21 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0003t0001g0192 others(18): Show |
22 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-147+13487G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665483 | |||||||
| chr14:51665501 | CT | C | 2 | a0001c0003t0001g0045 a0001c0003t0001g0046 |
4 | NA18970.hp2 NA19002.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147+13507delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51665501 | ||||||
| chr14:51665514 | C | T | 7 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(4): Show |
9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+13518C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665514 | |||||||
| chr14:51665518 | C | T | 1 | a0001c0003t0001g0049 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-147+13522C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665518 | |||||||
| chr14:51665613 | A | G | 99 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(96): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-147+13617A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665613 | |||||||
| chr14:51665667 | T | A | 1 | a0001c0003t0001g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-147+13671T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665667 | |||||||
| chr14:51665701 | C | T | 1 | a0001c0002t0002g0222 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-147+13705C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665701 | |||||||
| chr14:51665769 | T | C | 9 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0003t0001g0192 others(6): Show |
10 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-147+13773T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665769 | |||||||
| chr14:51665787 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-147+13791G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665787 | |||||||
| chr14:51665906 | C | T | 1 | a0001c0002t0001g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-147+13910C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665906 | |||||||
| chr14:51665979 | G | A | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+13983G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665979 | |||||||
| chr14:51666109 | T | C | 1 | a0002c0008t0009g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-147+14113T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666109 | |||||||
| chr14:51666332 | A | G | 4 | a0001c0002t0001g0033 a0001c0002t0001g0177 a0001c0002t0001g0178 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147+14336A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666332 | |||||||
| chr14:51666410 | T | A | 1 | a0001c0006t0003g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-147+14414T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666410 | |||||||
| chr14:51666428 | A | G | 3 | a0001c0002t0001g0202 a0001c0002t0001g0212 a0001c0002t0001g0213 |
3 | HG01884.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-147+14432A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666428 | |||||||
| chr14:51666515 | G | A | 25 | a0001c0001t0002g0176 a0001c0004t0001g0023 a0001c0004t0001g0050 others(22): Show |
28 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-147+14519G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666515 | |||||||
| chr14:51666750 | T | A | 1 | a0001c0002t0017g0209 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-147+14754T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666750 | |||||||
| chr14:51666926 | G | A | 1 | a0001c0002t0001g0219 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-147+14930G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666926 | |||||||
| chr14:51667006 | G | A | 6 | a0001c0001t0002g0176 a0001c0004t0012g0180 a0001c0004t0016g0072 others(3): Show |
6 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147+15010G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667006 | |||||||
| chr14:51667039 | C | T | 1 | a0001c0001t0002g0029 | 2 | NA18984.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-147+15043C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667039 | |||||||
| chr14:51667060 | G | A | 1 | a0001c0003t0001g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-147+15064G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667060 | |||||||
| chr14:51667080 | G | C | 74 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(71): Show |
99 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-147+15084G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667080 | |||||||
| chr14:51667282 | C | A | 8 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(5): Show |
9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-147+15286C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667282 | |||||||
| chr14:51667360 | C | T | 2 | a0001c0002t0014g0238 a0001c0002t0015g0235 |
2 | HG01496.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-147+15364C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667360 | |||||||
| chr14:51667378 | T | C | 1 | a0001c0003t0001g0293 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-147+15382T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667378 | |||||||
| chr14:51667636 | C | T | 13 | a0001c0001t0002g0030 a0001c0001t0002g0051 a0001c0001t0002g0052 others(10): Show |
13 | HG00738.hp1 HG01168.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.-147+15640C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667636 | |||||||
| chr14:51667669 | C | A | 210 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(207): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-147+15673C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667669 | |||||||
| chr14:51668316 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-147+16320T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668316 | |||||||
| chr14:51668405 | C | G | 1 | a0001c0002t0001g0221 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-147+16409C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668405 | |||||||
| chr14:51668438 | T | C | 5 | a0001c0006t0003g0011 a0001c0006t0003g0150 a0001c0006t0003g0152 others(2): Show |
7 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-147+16442T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668438 | |||||||
| chr14:51668466 | C | T | 5 | a0001c0002t0001g0076 a0001c0004t0001g0141 a0001c0004t0001g0142 others(2): Show |
5 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-147+16470C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668466 | |||||||
| chr14:51668496 | G | C | 1 | a0001c0002t0001g0216 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-147+16500G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668496 | |||||||
| chr14:51668634 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-147+16638G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668634 | |||||||
| chr14:51668638 | G | A | 139 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(136): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-147+16642G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668638 | |||||||
| chr14:51668818 | C | T | 1 | a0002c0008t0009g0281 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-147+16822C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668818 | |||||||
| chr14:51668868 | C | T | 3 | a0001c0001t0011g0130 a0001c0001t0011g0131 a0001c0001t0024g0123 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-147+16872C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668868 | |||||||
| chr14:51669055 | A | G | 2 | a0001c0002t0001g0201 a0001c0002t0001g0215 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-147+17059A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51669055 | |||||||
| chr14:51669058 | T | C | 2 | a0001c0003t0001g0096 a0001c0003t0001g0097 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-147+17062T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51669058 | |||||||
| chr14:51669172 | T | TATCTGGC others(720): Show |
2 | a0001c0004t0005g0183 a0001c0004t0005g0184 |
2 | HG02083.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-147+17196_-147+17 others(733): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51669172 | ||||||
| chr14:51669172 | T | TATCTGGC others(721): Show |
2 | a0001c0004t0005g0188 a0001c0004t0005g0282 |
2 | NA19055.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-147+17196_-147+17 others(734): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51669172 | ||||||
| chr14:51669492 | A | G | 1 | a0001c0003t0001g0299 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-147+17496A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51669492 | |||||||
| chr14:51669514 | G | T | 1 | a0001c0001t0002g0170 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-147+17518G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51669514 | |||||||
| chr14:51669849 | G | GCAAAATT others(315): Show |
7 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(4): Show |
9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+17863_-147+17 others(328): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51669849 | ||||||
| chr14:51669994 | C | T | 72 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(69): Show |
96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-147+17998C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51669994 | |||||||
| chr14:51670012 | C | T | 109 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(106): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-147+18016C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670012 | |||||||
| chr14:51670037 | A | C | 8 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(5): Show |
9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-147+18041A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670037 | |||||||
| chr14:51670039 | A | T | 2 | a0001c0001t0002g0041 a0001c0001t0002g0301 |
3 | HG01256.hp2 HG01258.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-147+18043A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670039 | |||||||
| chr14:51670070 | G | T | 109 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(106): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-147+18074G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670070 | |||||||
| chr14:51670098 | G | A | 1 | a0001c0003t0001g0287 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-147+18102G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670098 | |||||||
| chr14:51670124 | T | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+18128T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670124 | |||||||
| chr14:51670255 | A | T | 2 | a0001c0001t0002g0065 a0001c0001t0002g0066 |
2 | NA18951.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-147+18259A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670255 | |||||||
| chr14:51670350 | A | G | 110 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(107): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-147+18354A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670350 | |||||||
| chr14:51670398 | G | T | 1 | a0001c0001t0002g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-147+18402G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670398 | |||||||
| chr14:51670530 | A | G | 1 | a0001c0002t0001g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-147+18534A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670530 | |||||||
| chr14:51670707 | G | A | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+18711G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670707 | |||||||
| chr14:51670749 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-147+18753G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670749 | |||||||
| chr14:51670809 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-147+18813C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670809 | |||||||
| chr14:51670823 | T | C | 13 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(10): Show |
15 | HG01358.hp1 HG02083.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-147+18827T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670823 | |||||||
| chr14:51670860 | T | A | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-18831T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670860 | |||||||
| chr14:51670926 | C | T | 5 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(2): Show |
5 | HG02723.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-146-18765C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670926 | |||||||
| chr14:51670936 | C | T | 1 | a0001c0002t0001g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-146-18755C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670936 | |||||||
| chr14:51670937 | G | A | 2 | a0001c0002t0002g0200 a0001c0005t0001g0288 |
2 | HG02523.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-146-18754G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670937 | |||||||
| chr14:51670943 | G | A | 4 | a0001c0006t0003g0011 a0001c0006t0003g0150 a0001c0006t0003g0165 others(1): Show |
6 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-146-18748G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670943 | |||||||
| chr14:51671038 | T | G | 215 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(212): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-146-18653T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671038 | |||||||
| chr14:51671050 | A | T | 2 | a0001c0002t0001g0201 a0001c0002t0001g0215 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-146-18641A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671050 | |||||||
| chr14:51671069 | C | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0064 a0001c0001t0002g0156 |
4 | HG00099.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-18622C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671069 | |||||||
| chr14:51671155 | A | G | 2 | a0001c0001t0002g0029 a0001c0002t0001g0213 |
3 | HG03516.hp1 NA18984.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-146-18536A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671155 | |||||||
| chr14:51671177 | C | T | 3 | a0001c0003t0001g0017 a0001c0003t0001g0256 a0001c0003t0001g0257 |
5 | HG01081.hp2 HG01106.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-146-18514C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671177 | |||||||
| chr14:51671279 | T | TC | 27 | a0001c0001t0002g0176 a0001c0003t0001g0059 a0001c0004t0001g0023 others(24): Show |
31 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-146-18412_-146-18 others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671279 | |||||||
| chr14:51671342 | G | C | 8 | a0001c0002t0001g0286 a0001c0005t0001g0007 a0001c0005t0001g0010 others(5): Show |
14 | HG02074.hp1 HG02523.hp2 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.-146-18349G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671342 | |||||||
| chr14:51671376 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-146-18315C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671376 | |||||||
| chr14:51671459 | T | C | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-18232T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671459 | |||||||
| chr14:51671524 | A | G | 4 | a0001c0001t0001g0166 a0001c0001t0002g0084 a0001c0001t0002g0120 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-18167A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671524 | |||||||
| chr14:51671527 | G | T | 1 | a0001c0002t0001g0187 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-146-18164G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671527 | |||||||
| chr14:51671569 | G | A | 1 | a0001c0003t0001g0259 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-146-18122G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671569 | |||||||
| chr14:51671676 | C | T | 213 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(210): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-146-18015C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671676 | |||||||
| chr14:51671901 | T | G | 1 | a0001c0003t0001g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-146-17790T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671901 | |||||||
| chr14:51671930 | A | G | 111 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(108): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-146-17761A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671930 | |||||||
| chr14:51672079 | T | C | 1 | a0001c0003t0001g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-146-17612T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672079 | |||||||
| chr14:51672136 | A | G | 2 | a0001c0004t0016g0072 a0001c0006t0022g0161 |
2 | HG01433.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-146-17555A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672136 | |||||||
| chr14:51672417 | C | T | 1 | a0001c0005t0001g0296 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-146-17274C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672417 | |||||||
| chr14:51672488 | C | A | 1 | a0001c0002t0001g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-146-17203C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672488 | |||||||
| chr14:51672607 | G | T | 1 | a0001c0003t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-146-17084G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672607 | |||||||
| chr14:51672886 | C | T | 3 | a0001c0001t0006g0021 a0001c0001t0006g0063 a0001c0001t0023g0062 |
4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-16805C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672886 | |||||||
| chr14:51673067 | G | A | 7 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(4): Show |
8 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-146-16624G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673067 | |||||||
| chr14:51673237 | C | G | 2 | a0001c0002t0001g0210 a0001c0003t0001g0208 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-146-16454C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673237 | |||||||
| chr14:51673323 | T | A | 1 | a0001c0003t0001g0260 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-146-16368T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673323 | |||||||
| chr14:51673337 | T | G | 217 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(214): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-146-16354T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673337 | |||||||
| chr14:51673546 | T | G | 5 | a0001c0003t0001g0044 a0001c0003t0001g0252 a0001c0003t0001g0254 others(2): Show |
6 | HG02015.hp1 NA18953.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.-146-16145T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673546 | |||||||
| chr14:51673704 | T | C | 7 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(4): Show |
9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-146-15987T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673704 | |||||||
| chr14:51673978 | A | T | 1 | a0001c0003t0001g0250 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-146-15713A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673978 | |||||||
| chr14:51673979 | T | C | 1 | a0001c0002t0001g0133 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-146-15712T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673979 | |||||||
| chr14:51674253 | C | T | 1 | a0001c0004t0001g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-146-15438C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674253 | |||||||
| chr14:51674420 | T | C | 1 | a0001c0002t0008g0018 | 3 | NA18957.hp2 NA18961.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-146-15271T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674420 | |||||||
| chr14:51674460 | C | T | 1 | a0005c0012t0002g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-146-15231C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674460 | |||||||
| chr14:51674626 | T | C | 1 | a0001c0004t0001g0039 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-146-15065T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674626 | |||||||
| chr14:51674748 | G | A | 1 | a0001c0013t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-146-14943G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674748 | |||||||
| chr14:51674927 | A | G | 13 | a0001c0001t0002g0030 a0001c0001t0002g0051 a0001c0001t0002g0052 others(10): Show |
13 | HG00738.hp1 HG01168.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.-146-14764A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674927 | |||||||
| chr14:51674929 | G | T | 25 | a0001c0001t0002g0176 a0001c0004t0001g0023 a0001c0004t0001g0050 others(22): Show |
28 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-146-14762G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674929 | |||||||
| chr14:51674955 | G | A | 138 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(135): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-146-14736G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674955 | |||||||
| chr14:51674984 | G | T | 3 | a0001c0001t0007g0119 a0001c0001t0007g0139 a0001c0001t0007g0157 |
3 | HG00733.hp2 HG01109.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-146-14707G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674984 | |||||||
| chr14:51675132 | G | A | 1 | a0001c0001t0002g0284 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-146-14559G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51675132 | |||||||
| chr14:51675221 | C | T | 1 | a0001c0002t0001g0164 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-146-14470C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51675221 | |||||||
| chr14:51675564 | T | C | 1 | a0001c0013t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-146-14127T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51675564 | |||||||
| chr14:51676001 | A | T | 1 | a0001c0003t0001g0046 | 2 | NA18970.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-146-13690A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676001 | |||||||
| chr14:51676013 | C | T | 1 | a0001c0002t0001g0240 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-146-13678C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676013 | |||||||
| chr14:51676029 | G | A | 4 | a0001c0002t0001g0093 a0001c0004t0001g0050 a0001c0004t0001g0068 others(1): Show |
4 | HG00639.hp1 HG01109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-13662G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676029 | |||||||
| chr14:51676088 | T | G | 1 | a0001c0002t0001g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-146-13603T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676088 | |||||||
| chr14:51676120 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-146-13571A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676120 | |||||||
| chr14:51676168 | G | C | 131 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(128): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.-146-13523G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676168 | |||||||
| chr14:51676514 | G | T | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-13177G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676514 | |||||||
| chr14:51676805 | T | G | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-12886T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676805 | |||||||
| chr14:51676881 | C | T | 1 | a0001c0002t0001g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-146-12810C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676881 | |||||||
| chr14:51676960 | A | G | 1 | a0001c0004t0001g0039 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-146-12731A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676960 | |||||||
| chr14:51676976 | C | T | 128 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(125): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-146-12715C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676976 | |||||||
| chr14:51677121 | G | T | 1 | a0001c0002t0001g0234 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-146-12570G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677121 | |||||||
| chr14:51677424 | G | A | 2 | a0001c0003t0001g0192 a0003c0010t0001g0073 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-146-12267G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677424 | |||||||
| chr14:51677697 | T | C | 1 | a0001c0002t0001g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-146-11994T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677697 | |||||||
| chr14:51677719 | A | G | 208 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(205): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.-146-11972A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677719 | |||||||
| chr14:51677726 | G | A | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-11965G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677726 | |||||||
| chr14:51677875 | T | C | 271 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(268): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-146-11816T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677875 | |||||||
| chr14:51678154 | T | C | 118 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(115): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-146-11537T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678154 | |||||||
| chr14:51678287 | G | C | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-11404G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678287 | |||||||
| chr14:51678387 | T | C | 274 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(271): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-146-11304T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678387 | |||||||
| chr14:51678427 | A | G | 1 | a0001c0003t0001g0049 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-146-11264A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678427 | |||||||
| chr14:51678526 | T | C | 119 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(116): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-146-11165T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678526 | |||||||
| chr14:51678597 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-146-11094G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678597 | |||||||
| chr14:51678941 | C | T | 101 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(98): Show |
127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-146-10750C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678941 | |||||||
| chr14:51678978 | T | G | 1 | a0001c0003t0001g0046 | 2 | NA18970.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-146-10713T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678978 | |||||||
| chr14:51679044 | G | A | 1 | a0001c0013t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-146-10647G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679044 | |||||||
| chr14:51679131 | C | G | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-146-10560C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679131 | |||||||
| chr14:51679271 | T | G | 1 | a0001c0003t0001g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-146-10420T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679271 | |||||||
| chr14:51679299 | C | CAT | 303 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(300): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-146-10392_-146-10 others(8): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679299 | |||||||
| chr14:51679406 | G | T | 49 | a0001c0002t0001g0003 a0001c0002t0001g0015 a0001c0002t0001g0028 others(46): Show |
60 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.-146-10285G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679406 | |||||||
| chr14:51679555 | C | CT | 8 | a0001c0002t0001g0143 a0001c0003t0001g0080 a0001c0003t0001g0245 others(5): Show |
8 | HG01175.hp1 HG02027.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-146-10118dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51679555 | ||||||
| chr14:51679555 | CT | C | 17 | a0001c0001t0002g0004 a0001c0001t0002g0115 a0001c0001t0002g0116 others(14): Show |
22 | HG01515.hp1 HG02083.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-146-10118delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51679555 | ||||||
| chr14:51679555 | CTT | C | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-146-10119_-146-10 others(8): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51679555 | ||||||
| chr14:51679735 | C | G | 4 | a0001c0002t0004g0042 a0001c0002t0004g0218 a0001c0002t0004g0233 others(1): Show |
5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-146-9956C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679735 | |||||||
| chr14:51679737 | T | G | 5 | a0001c0003t0001g0019 a0001c0003t0001g0224 a0001c0003t0001g0264 others(2): Show |
7 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-146-9954T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679737 | |||||||
| chr14:51679881 | C | T | 1 | a0001c0003t0001g0192 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-146-9810C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679881 | |||||||
| chr14:51680119 | G | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0064 a0001c0001t0002g0156 |
4 | HG00099.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-9572G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51680119 | |||||||
| chr14:51680764 | AT | A | 125 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(122): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-146-8920delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51680764 | ||||||
| chr14:51680813 | T | G | 1 | a0001c0001t0019g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-146-8878T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51680813 | |||||||
| chr14:51681123 | C | T | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-8568C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681123 | |||||||
| chr14:51681300 | A | G | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-8391A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681300 | |||||||
| chr14:51681362 | TG | T | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-8328delG | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681362 | |||||||
| chr14:51681366 | G | C | 1 | a0001c0003t0001g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-146-8325G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681366 | |||||||
| chr14:51681598 | A | G | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-8093A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681598 | |||||||
| chr14:51681898 | T | C | 1 | a0001c0001t0019g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-146-7793T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681898 | |||||||
| chr14:51681938 | T | G | 1 | a0001c0003t0001g0079 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-146-7753T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681938 | |||||||
| chr14:51681976 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-146-7715C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681976 | |||||||
| chr14:51682032 | T | C | 1 | a0001c0007t0001g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-146-7659T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682032 | |||||||
| chr14:51682040 | A | G | 3 | a0001c0004t0016g0072 a0002c0008t0009g0074 a0002c0008t0009g0281 |
3 | HG02258.hp2 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-146-7651A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682040 | |||||||
| chr14:51682091 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-146-7600A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682091 | |||||||
| chr14:51682234 | C | A | 1 | a0001c0002t0001g0164 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-146-7457C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682234 | |||||||
| chr14:51682499 | G | C | 4 | a0001c0004t0012g0180 a0001c0004t0016g0072 a0002c0008t0009g0074 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-7192G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682499 | |||||||
| chr14:51682576 | T | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-7115T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682576 | |||||||
| chr14:51682773 | C | T | 1 | a0001c0013t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-146-6918C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682773 | |||||||
| chr14:51682822 | A | G | 1 | a0001c0002t0001g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-146-6869A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682822 | |||||||
| chr14:51682925 | G | A | 1 | a0001c0002t0001g0174 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-146-6766G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682925 | |||||||
| chr14:51682930 | C | T | 117 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(114): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-146-6761C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682930 | |||||||
| chr14:51682960 | A | G | 1 | a0001c0003t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-146-6731A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682960 | |||||||
| chr14:51683037 | C | A | 2 | a0001c0003t0001g0192 a0003c0010t0001g0073 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-146-6654C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683037 | |||||||
| chr14:51683045 | C | G | 1 | a0001c0002t0001g0239 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-146-6646C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683045 | |||||||
| chr14:51683050 | T | C | 120 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(117): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-146-6641T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683050 | |||||||
| chr14:51683079 | A | G | 1 | a0001c0004t0001g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-146-6612A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683079 | |||||||
| chr14:51683116 | A | G | 76 | a0001c0002t0001g0164 a0001c0003t0001g0005 a0001c0003t0001g0006 others(73): Show |
101 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-146-6575A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683116 | |||||||
| chr14:51683161 | T | C | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-6530T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683161 | |||||||
| chr14:51683348 | CAGCAATG others(5): Show |
C | 1 | a0001c0003t0001g0293 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6339_-146-632 others(16): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51683348 | ||||||
| chr14:51683367 | T | G | 1 | a0001c0003t0001g0293 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6324T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683367 | |||||||
| chr14:51683368 | C | G | 1 | a0001c0003t0001g0293 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6323C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683368 | |||||||
| chr14:51683369 | T | A | 1 | a0001c0003t0001g0293 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6322T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683369 | |||||||
| chr14:51683370 | C | G | 1 | a0001c0003t0001g0293 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6321C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683370 | |||||||
| chr14:51683371 | C | A | 1 | a0001c0003t0001g0293 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6320C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683371 | |||||||
| chr14:51683445 | AT | A | 118 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(115): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-146-6233delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51683445 | ||||||
| chr14:51683479 | G | A | 1 | a0005c0012t0002g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-146-6212G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683479 | |||||||
| chr14:51683489 | G | C | 77 | a0001c0002t0001g0164 a0001c0003t0001g0005 a0001c0003t0001g0006 others(74): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-146-6202G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683489 | |||||||
| chr14:51683572 | C | T | 1 | a0001c0004t0001g0039 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-146-6119C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683572 | |||||||
| chr14:51683687 | G | A | 117 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-6004G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683687 | |||||||
| chr14:51683692 | A | G | 1 | a0001c0002t0001g0175 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-146-5999A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683692 | |||||||
| chr14:51683895 | T | C | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-5796T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683895 | |||||||
| chr14:51684117 | G | A | 2 | a0001c0003t0001g0044 a0001c0003t0001g0254 |
3 | NA18953.hp1 NA18990.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-146-5574G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684117 | |||||||
| chr14:51684146 | T | C | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-5545T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684146 | |||||||
| chr14:51684158 | C | T | 1 | a0001c0004t0005g0183 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-146-5533C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684158 | |||||||
| chr14:51684161 | T | TA | 6 | a0001c0002t0001g0092 a0001c0002t0001g0126 a0001c0002t0014g0238 others(3): Show |
6 | HG01496.hp1 HG02040.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-146-5517dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51684161 | ||||||
| chr14:51684161 | TA | T | 117 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-5517delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51684161 | ||||||
| chr14:51684180 | A | G | 2 | a0001c0003t0001g0192 a0003c0010t0001g0073 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-146-5511A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684180 | |||||||
| chr14:51684222 | G | A | 1 | a0002c0008t0009g0281 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-146-5469G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684222 | |||||||
| chr14:51684486 | G | A | 100 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(97): Show |
126 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-146-5205G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684486 | |||||||
| chr14:51684557 | C | T | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-5134C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684557 | |||||||
| chr14:51684621 | A | G | 117 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-5070A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684621 | |||||||
| chr14:51684728 | C | T | 1 | a0001c0003t0001g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-146-4963C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684728 | |||||||
| chr14:51684752 | T | C | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-4939T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684752 | |||||||
| chr14:51684756 | A | T | 75 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(72): Show |
99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-146-4935A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684756 | |||||||
| chr14:51684821 | T | G | 1 | a0001c0006t0003g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-146-4870T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684821 | |||||||
| chr14:51684907 | G | A | 2 | a0001c0002t0014g0238 a0001c0002t0015g0235 |
2 | HG01496.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-146-4784G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684907 | |||||||
| chr14:51685159 | A | G | 1 | a0001c0001t0002g0114 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-146-4532A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685159 | |||||||
| chr14:51685186 | T | C | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-4505T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685186 | |||||||
| chr14:51685464 | G | A | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-146-4227G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685464 | |||||||
| chr14:51685582 | A | G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0199 a0001c0001t0002g0207 others(1): Show |
6 | HG01074.hp2 HG01099.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-146-4109A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685582 | |||||||
| chr14:51685803 | G | A | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-3888G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685803 | |||||||
| chr14:51685819 | TA | T | 117 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-3870delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51685819 | ||||||
| chr14:51685883 | G | A | 117 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-3808G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685883 | |||||||
| chr14:51686019 | C | T | 1 | a0001c0002t0001g0164 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-146-3672C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51686019 | |||||||
| chr14:51686106 | T | A | 117 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-3585T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51686106 | |||||||
| chr14:51686152 | T | TA | 77 | a0001c0002t0001g0164 a0001c0003t0001g0005 a0001c0003t0001g0006 others(74): Show |
102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-146-3537dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51686152 | ||||||
| chr14:51686779 | T | A | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-146-2912T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51686779 | |||||||
| chr14:51686806 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-146-2885A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51686806 | |||||||
| chr14:51686858 | TTAAG | T | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0007t0001g0057 others(1): Show |
4 | HG02630.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-2831_-146-282 others(8): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51686858 | ||||||
| chr14:51686894 | A | G | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-2797A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51686894 | |||||||
| chr14:51687054 | C | A | 117 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-2637C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687054 | |||||||
| chr14:51687087 | C | T | 117 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-2604C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687087 | |||||||
| chr14:51687238 | A | T | 76 | a0001c0002t0001g0164 a0001c0003t0001g0005 a0001c0003t0001g0006 others(73): Show |
101 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-146-2453A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687238 | |||||||
| chr14:51687336 | A | G | 1 | a0003c0010t0001g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-146-2355A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687336 | |||||||
| chr14:51687359 | G | A | 1 | a0003c0010t0001g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-146-2332G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687359 | |||||||
| chr14:51687539 | T | G | 8 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(5): Show |
10 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-146-2152T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687539 | |||||||
| chr14:51687542 | T | TA | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-2148dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51687542 | ||||||
| chr14:51687632 | C | G | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0007t0001g0057 others(1): Show |
4 | HG02630.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-2059C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687632 | |||||||
| chr14:51687644 | C | T | 1 | a0001c0003t0001g0259 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-146-2047C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687644 | |||||||
| chr14:51687654 | T | C | 1 | a0001c0002t0001g0241 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-146-2037T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687654 | |||||||
| chr14:51687779 | C | T | 2 | a0001c0003t0001g0192 a0003c0010t0001g0073 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-146-1912C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687779 | |||||||
| chr14:51687809 | A | T | 1 | a0001c0001t0002g0304 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-146-1882A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687809 | |||||||
| chr14:51687859 | A | C | 13 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(10): Show |
16 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-146-1832A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687859 | |||||||
| chr14:51687894 | C | G | 1 | a0001c0002t0001g0186 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-146-1797C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687894 | |||||||
| chr14:51687914 | T | G | 1 | a0001c0003t0001g0262 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-146-1777T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687914 | |||||||
| chr14:51688114 | G | A | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-1577G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688114 | |||||||
| chr14:51688128 | T | G | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-146-1563T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688128 | |||||||
| chr14:51688159 | T | C | 3 | a0001c0001t0006g0021 a0001c0001t0006g0063 a0001c0001t0023g0062 |
4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-1532T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688159 | |||||||
| chr14:51688327 | A | C | 2 | a0001c0003t0001g0192 a0003c0010t0001g0073 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-146-1364A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688327 | |||||||
| chr14:51688361 | TCGAGTAA others(4): Show |
T | 1 | a0001c0004t0005g0282 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-146-1328_-146-131 others(15): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51688361 | ||||||
| chr14:51688362 | C | T | 1 | a0001c0003t0001g0290 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-146-1329C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688362 | |||||||
| chr14:51688363 | G | A | 1 | a0001c0001t0002g0304 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-146-1328G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688363 | |||||||
| chr14:51688444 | A | G | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-1247A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688444 | |||||||
| chr14:51688459 | C | G | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-1232C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688459 | |||||||
| chr14:51688527 | C | T | 1 | a0001c0006t0003g0151 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-146-1164C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688527 | |||||||
| chr14:51688630 | C | T | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-146-1061C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688630 | |||||||
| chr14:51688763 | T | C | 1 | a0001c0002t0001g0177 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-146-928T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688763 | |||||||
| chr14:51688874 | A | G | 1 | a0001c0003t0001g0137 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-146-817A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688874 | |||||||
| chr14:51688977 | AT | A | 3 | a0001c0002t0001g0028 a0001c0002t0001g0124 a0001c0002t0001g0143 |
4 | HG02027.hp2 NA18945.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-708delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51688977 | ||||||
| chr14:51689123 | G | A | 1 | a0001c0005t0001g0288 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-146-568G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689123 | |||||||
| chr14:51689128 | G | T | 1 | a0001c0002t0001g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-146-563G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689128 | |||||||
| chr14:51689267 | T | C | 8 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(5): Show |
9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-146-424T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689267 | |||||||
| chr14:51689279 | C | G | 16 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(13): Show |
17 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-146-412C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689279 | |||||||
| chr14:51689423 | G | T | 116 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(113): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-146-268G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689423 | |||||||
| chr14:51689652 | C | T | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-39C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689652 | |||||||
| chr14:51690144 | A | G | 1 | a0001c0001t0019g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.99+209A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690144 | |||||||
| chr14:51690334 | T | C | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+399T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690334 | |||||||
| chr14:51690417 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.99+482A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690417 | |||||||
| chr14:51690662 | G | A | 1 | a0001c0002t0001g0077 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.99+727G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690662 | |||||||
| chr14:51690747 | A | G | 1 | a0001c0003t0001g0255 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.99+812A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690747 | |||||||
| chr14:51690850 | A | AT | 18 | a0001c0002t0001g0194 a0001c0004t0001g0023 a0001c0004t0001g0039 others(15): Show |
20 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+924dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51690850 | ||||||
| chr14:51690971 | A | G | 96 | a0001c0002t0001g0164 a0001c0002t0001g0194 a0001c0003t0001g0005 others(93): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.99+1036A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690971 | |||||||
| chr14:51691065 | T | A | 2 | a0001c0003t0001g0192 a0003c0010t0001g0073 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.99+1130T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691065 | |||||||
| chr14:51691118 | A | G | 1 | a0001c0001t0024g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.99+1183A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691118 | |||||||
| chr14:51691187 | A | G | 200 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(197): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.99+1252A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691187 | |||||||
| chr14:51691270 | T | C | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+1335T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691270 | |||||||
| chr14:51691352 | A | G | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.99+1417A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691352 | |||||||
| chr14:51691380 | G | A | 1 | a0001c0006t0003g0151 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99+1445G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691380 | |||||||
| chr14:51691451 | C | T | 4 | a0001c0001t0002g0004 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
8 | NA18954.hp2 NA18957.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1516C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691451 | |||||||
| chr14:51691585 | TTGA | T | 55 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(52): Show |
73 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.99+1652_99+1654del others(3): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691585 | ||||||
| chr14:51691586 | TGA | T | 15 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0046 others(12): Show |
18 | HG00544.hp2 HG01175.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+1652_99+1653del others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691586 | |||||||
| chr14:51691588 | A | AT | 13 | a0001c0002t0001g0003 a0001c0002t0001g0008 a0001c0002t0001g0037 others(10): Show |
13 | HG01175.hp2 HG01243.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1677dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | ||||||
| chr14:51691588 | A | T | 1 | a0001c0003t0001g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.99+1653A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691588 | |||||||
| chr14:51691588 | AT | A | 11 | a0001c0002t0001g0093 a0001c0002t0001g0126 a0001c0002t0001g0174 others(8): Show |
12 | HG00099.hp1 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+1677delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | ||||||
| chr14:51691588 | ATT | A | 10 | a0001c0004t0005g0183 a0001c0004t0005g0188 a0001c0004t0005g0282 others(7): Show |
11 | HG01358.hp1 HG01433.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+1676_99+1677del others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | ||||||
| chr14:51691588 | ATTT | A | 9 | a0001c0001t0007g0157 a0001c0004t0001g0141 a0001c0004t0001g0142 others(6): Show |
9 | HG01109.hp2 HG02083.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+1675_99+1677del others(3): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | ||||||
| chr14:51691588 | ATTTT | A | 8 | a0001c0001t0002g0065 a0001c0001t0002g0158 a0001c0001t0002g0159 others(5): Show |
8 | HG00733.hp2 HG01261.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1674_99+1677del others(4): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | ||||||
| chr14:51691588 | ATTTTT | A | 91 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(88): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+1673_99+1677del others(5): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | ||||||
| chr14:51691828 | C | T | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.99+1893C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691828 | |||||||
| chr14:51691843 | C | T | 10 | a0001c0001t0001g0111 a0001c0001t0002g0058 a0001c0001t0002g0112 others(7): Show |
10 | HG01891.hp1 HG02486.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+1908C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691843 | |||||||
| chr14:51691875 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+1940G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691875 | |||||||
| chr14:51691955 | A | AAT | 185 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(182): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.99+2025_99+2026dup others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691955 | ||||||
| chr14:51691958 | A | T | 1 | a0001c0004t0001g0039 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.99+2023A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691958 | |||||||
| chr14:51692111 | A | G | 1 | a0001c0002t0001g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+2176A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692111 | |||||||
| chr14:51692115 | G | T | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 |
3 | HG01256.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.99+2180G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692115 | |||||||
| chr14:51692228 | ATT | A | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+2296_99+2297del others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692228 | ||||||
| chr14:51692305 | A | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+2370A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692305 | |||||||
| chr14:51692355 | T | C | 1 | a0001c0001t0002g0300 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.99+2420T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692355 | |||||||
| chr14:51692420 | A | G | 3 | a0001c0002t0001g0090 a0001c0002t0001g0093 a0001c0002t0001g0094 |
3 | NA18972.hp1 NA18986.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.99+2485A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692420 | |||||||
| chr14:51692472 | A | ATG | 128 | a0001c0001t0002g0030 a0001c0001t0002g0051 a0001c0001t0002g0052 others(125): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.99+2559_99+2560dup others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692472 | ||||||
| chr14:51692472 | A | ATGTG | 85 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0198 others(82): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.99+2557_99+2560dup others(4): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692472 | ||||||
| chr14:51692472 | A | ATGTGTG | 7 | a0001c0001t0001g0166 a0001c0001t0002g0084 a0001c0001t0002g0113 others(4): Show |
7 | HG00544.hp1 HG02135.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+2555_99+2560dup others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692472 | ||||||
| chr14:51692472 | ATG | A | 73 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(70): Show |
96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.99+2559_99+2560del others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692472 | ||||||
| chr14:51692482 | G | GTA | 7 | a0001c0002t0001g0031 a0001c0002t0001g0182 a0001c0002t0001g0185 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+2548_99+2549ins others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692482 | ||||||
| chr14:51692510 | G | T | 1 | a0001c0002t0001g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99+2575G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692510 | |||||||
| chr14:51692854 | A | G | 1 | a0001c0003t0001g0261 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.99+2919A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692854 | |||||||
| chr14:51692871 | A | T | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.99+2936A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692871 | |||||||
| chr14:51692878 | C | G | 110 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(107): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.99+2943C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692878 | |||||||
| chr14:51692965 | A | G | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3030A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692965 | |||||||
| chr14:51692987 | C | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3052C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692987 | |||||||
| chr14:51693025 | G | T | 1 | a0001c0003t0001g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.99+3090G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693025 | |||||||
| chr14:51693036 | T | A | 1 | a0001c0003t0001g0266 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.99+3101T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693036 | |||||||
| chr14:51693211 | G | A | 1 | a0001c0006t0003g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+3276G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693211 | |||||||
| chr14:51693354 | G | A | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3419G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693354 | |||||||
| chr14:51693391 | A | G | 2 | a0001c0004t0005g0183 a0001c0004t0005g0188 |
2 | NA18994.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.99+3456A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693391 | |||||||
| chr14:51693453 | G | A | 1 | a0001c0002t0001g0230 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.99+3518G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693453 | |||||||
| chr14:51693476 | C | G | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3541C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693476 | |||||||
| chr14:51693521 | T | C | 5 | a0001c0002t0001g0230 a0001c0002t0004g0042 a0001c0002t0004g0218 others(2): Show |
6 | HG00280.hp2 HG00733.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+3586T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693521 | |||||||
| chr14:51693622 | T | TG | 303 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(300): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.99+3688dupG | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51693622 | ||||||
| chr14:51693704 | G | T | 74 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(71): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.99+3769G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693704 | |||||||
| chr14:51693889 | C | T | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.99+3954C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693889 | |||||||
| chr14:51693933 | A | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3998A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693933 | |||||||
| chr14:51693976 | G | A | 10 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(7): Show |
12 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+4041G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693976 | |||||||
| chr14:51694120 | A | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0205 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.100-4022A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694120 | |||||||
| chr14:51694280 | G | A | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3862G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694280 | |||||||
| chr14:51694303 | T | C | 188 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(185): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.100-3839T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694303 | |||||||
| chr14:51694415 | T | A | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.100-3727T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694415 | |||||||
| chr14:51694719 | T | C | 1 | a0001c0001t0002g0127 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.100-3423T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694719 | |||||||
| chr14:51694910 | CCATGGCC others(267): Show |
C | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3229_100-2956d others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51694910 | ||||||
| chr14:51694968 | A | G | 3 | a0001c0001t0006g0021 a0001c0001t0006g0063 a0001c0001t0023g0062 |
4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3174A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694968 | |||||||
| chr14:51694978 | A | G | 77 | a0001c0002t0001g0164 a0001c0003t0001g0005 a0001c0003t0001g0006 others(74): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.100-3164A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694978 | |||||||
| chr14:51694982 | G | A | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3160G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694982 | |||||||
| chr14:51695069 | C | CAGTCACA others(4): Show |
1 | a0001c0002t0001g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.100-3072_100-3062d others(13): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51695069 | ||||||
| chr14:51695085 | A | C | 1 | a0001c0003t0001g0044 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.100-3057A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695085 | |||||||
| chr14:51695170 | G | A | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-2972G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695170 | |||||||
| chr14:51695224 | T | A | 4 | a0001c0001t0002g0026 a0001c0001t0002g0102 a0001c0001t0002g0103 others(1): Show |
5 | HG02132.hp1 NA18949.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-2918T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695224 | |||||||
| chr14:51695374 | G | A | 206 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(203): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.100-2768G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695374 | |||||||
| chr14:51695387 | C | A | 2 | a0001c0002t0014g0238 a0001c0002t0015g0235 |
2 | HG01496.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.100-2755C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695387 | |||||||
| chr14:51695647 | C | G | 185 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(182): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.100-2495C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695647 | |||||||
| chr14:51695841 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.100-2301C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695841 | |||||||
| chr14:51696315 | C | T | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1827C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696315 | |||||||
| chr14:51696431 | A | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1711A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696431 | |||||||
| chr14:51696542 | G | C | 1 | a0004c0016t0002g0104 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.100-1600G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696542 | |||||||
| chr14:51696637 | C | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1505C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696637 | |||||||
| chr14:51696728 | C | T | 3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0021g0214 |
3 | HG02886.hp2 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.100-1414C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696728 | |||||||
| chr14:51696751 | C | CA | 182 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(179): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.100-1377dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51696751 | ||||||
| chr14:51696765 | A | AT | 8 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0036 others(5): Show |
11 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-1377_100-1376i others(3): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696765 | |||||||
| chr14:51696790 | A | C | 5 | a0001c0002t0001g0230 a0001c0002t0004g0042 a0001c0002t0004g0218 others(2): Show |
6 | HG00280.hp2 HG00733.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-1352A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696790 | |||||||
| chr14:51696845 | A | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1297A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696845 | |||||||
| chr14:51696866 | G | A | 209 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(206): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.100-1276G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696866 | |||||||
| chr14:51696871 | C | T | 1 | a0001c0003t0001g0259 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.100-1271C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696871 | |||||||
| chr14:51697086 | A | G | 1 | a0001c0002t0001g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100-1056A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697086 | |||||||
| chr14:51697332 | C | T | 64 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0002g0001 others(61): Show |
86 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.100-810C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697332 | |||||||
| chr14:51697409 | G | A | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-733G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697409 | |||||||
| chr14:51697710 | A | G | 1 | a0001c0002t0001g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.100-432A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697710 | |||||||
| chr14:51697791 | A | T | 8 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(5): Show |
9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-351A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697791 | |||||||
| chr14:51697831 | G | A | 1 | a0001c0001t0002g0041 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.100-311G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697831 | |||||||
| chr14:51698060 | G | A | 9 | a0001c0001t0002g0030 a0001c0001t0002g0051 a0001c0001t0002g0144 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-82G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51698060 | |||||||
| chr14:51698351 | GGACT | G | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+122_190+125del others(4): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 51698351 | ||||||
| chr14:51698365 | T | G | 179 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(176): Show |
230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.190+133T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698365 | |||||||
| chr14:51698408 | A | G | 197 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(194): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.190+176A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698408 | |||||||
| chr14:51698461 | C | G | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+229C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698461 | |||||||
| chr14:51698615 | A | C | 8 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0036 others(5): Show |
11 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.190+383A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698615 | |||||||
| chr14:51698703 | C | T | 1 | a0001c0004t0001g0071 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.190+471C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698703 | |||||||
| chr14:51698704 | G | T | 199 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(196): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.190+472G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698704 | |||||||
| chr14:51698735 | A | T | 77 | a0001c0002t0001g0164 a0001c0003t0001g0005 a0001c0003t0001g0006 others(74): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.190+503A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698735 | |||||||
| chr14:51698791 | T | A | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+559T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698791 | |||||||
| chr14:51698829 | C | A | 1 | a0001c0002t0001g0171 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.190+597C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698829 | |||||||
| chr14:51698898 | G | A | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.190+666G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698898 | |||||||
| chr14:51698932 | A | G | 1 | a0001c0002t0001g0135 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.190+700A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698932 | |||||||
| chr14:51699001 | G | A | 2 | a0001c0001t0002g0014 a0005c0012t0002g0206 |
4 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+769G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699001 | |||||||
| chr14:51699010 | T | C | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+778T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699010 | |||||||
| chr14:51699364 | A | G | 1 | a0001c0002t0013g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+1132A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699364 | |||||||
| chr14:51699534 | C | T | 7 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(4): Show |
8 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.190+1302C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699534 | |||||||
| chr14:51699571 | C | G | 2 | a0001c0001t0002g0145 a0001c0003t0001g0208 |
2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.190+1339C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699571 | |||||||
| chr14:51699608 | T | C | 1 | a0001c0006t0003g0151 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.190+1376T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699608 | |||||||
| chr14:51699627 | G | A | 1 | a0001c0002t0002g0200 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.190+1395G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699627 | |||||||
| chr14:51699701 | C | G | 2 | a0001c0002t0001g0201 a0001c0002t0001g0215 |
2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.191-1355C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699701 | |||||||
| chr14:51699836 | C | G | 1 | a0001c0003t0001g0273 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.191-1220C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699836 | |||||||
| chr14:51699837 | G | A | 14 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(11): Show |
16 | HG01358.hp1 HG01433.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.191-1219G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699837 | |||||||
| chr14:51699927 | TAAG | T | 3 | a0001c0003t0001g0020 a0001c0003t0001g0253 a0001c0003t0001g0272 |
5 | HG00544.hp2 HG02155.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.191-1128_191-1126d others(5): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699927 | |||||||
| chr14:51699939 | C | CT | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.191-1110dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 51699939 | ||||||
| chr14:51699956 | A | T | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.191-1100A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699956 | |||||||
| chr14:51699995 | A | G | 1 | a0001c0002t0001g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.191-1061A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699995 | |||||||
| chr14:51700011 | A | G | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-1045A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700011 | |||||||
| chr14:51700024 | C | T | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.191-1032C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700024 | |||||||
| chr14:51700102 | C | T | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.191-954C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700102 | |||||||
| chr14:51700105 | C | T | 1 | a0001c0002t0001g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.191-951C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700105 | |||||||
| chr14:51700402 | G | C | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.191-654G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700402 | |||||||
| chr14:51700687 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.191-369C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700687 | |||||||
| chr14:51700960 | G | A | 1 | a0001c0004t0005g0183 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.191-96G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700960 | |||||||
| chr14:51700983 | T | C | 2 | a0001c0004t0001g0039 a0001c0004t0016g0072 |
3 | HG02818.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.191-73T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700983 | |||||||
| chr14:51701191 | GA | G | 10 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(7): Show |
12 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.294+33delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701191 | |||||||
| chr14:51701200 | T | A | 11 | a0001c0001t0002g0027 a0001c0001t0007g0139 a0001c0002t0001g0194 others(8): Show |
13 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.294+41T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701200 | |||||||
| chr14:51701312 | G | GTA | 4 | a0001c0002t0001g0133 a0001c0003t0001g0297 a0001c0003t0001g0298 others(1): Show |
4 | HG02015.hp2 HG03139.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+166_294+167dup others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 51701312 | ||||||
| chr14:51701343 | ATTTTC | A | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.294+190_294+194del others(5): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 51701343 | ||||||
| chr14:51701372 | G | GAGTATAT others(20): Show |
4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+226_294+252dup others(27): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 51701372 | ||||||
| chr14:51701403 | A | G | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.294+244A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701403 | |||||||
| chr14:51701472 | GTA | G | 3 | a0001c0003t0001g0192 a0001c0004t0016g0072 a0003c0010t0001g0073 |
3 | HG02818.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+326_294+327del others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 51701472 | ||||||
| chr14:51701597 | A | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+438A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701597 | |||||||
| chr14:51701621 | G | A | 2 | a0001c0001t0011g0130 a0001c0001t0011g0131 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.294+462G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701621 | |||||||
| chr14:51701916 | A | C | 2 | a0001c0004t0001g0039 a0001c0004t0016g0072 |
3 | HG02818.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.295-596A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701916 | |||||||
| chr14:51702092 | A | G | 179 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(176): Show |
230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.295-420A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51702092 | |||||||
| chr14:51702123 | T | C | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-389T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51702123 | |||||||
| chr14:51702170 | T | C | 1 | a0001c0004t0001g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.295-342T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51702170 | |||||||
| chr14:51702301 | T | C | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.295-211T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51702301 | |||||||
| chr14:51702373 | G | A | 104 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(101): Show |
131 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.295-139G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51702373 | |||||||
| chr14:51702623 | T | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+35T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51702623 | |||||||
| chr14:51702847 | A | G | 1 | a0001c0003t0001g0078 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.371+259A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51702847 | |||||||
| chr14:51702955 | T | A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0110 |
2 | HG00597.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.371+367T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51702955 | |||||||
| chr14:51702988 | G | C | 1 | a0001c0001t0002g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.371+400G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51702988 | |||||||
| chr14:51703029 | G | T | 67 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(64): Show |
91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.371+441G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703029 | |||||||
| chr14:51703085 | A | G | 1 | a0001c0001t0007g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.371+497A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703085 | |||||||
| chr14:51703134 | C | A | 1 | a0001c0001t0002g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.371+546C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703134 | |||||||
| chr14:51703154 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.371+566G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703154 | |||||||
| chr14:51703399 | A | G | 2 | a0001c0004t0001g0039 a0001c0004t0016g0072 |
3 | HG02818.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.371+811A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703399 | |||||||
| chr14:51703481 | A | T | 1 | a0001c0004t0005g0282 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.371+893A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703481 | |||||||
| chr14:51703603 | C | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+1015C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703603 | |||||||
| chr14:51704024 | A | C | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.372-725A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704024 | |||||||
| chr14:51704072 | G | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0153 a0001c0001t0002g0154 |
5 | HG00673.hp1 NA18944.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.372-677G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704072 | |||||||
| chr14:51704119 | T | A | 1 | a0001c0003t0001g0262 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.372-630T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704119 | |||||||
| chr14:51704367 | C | T | 1 | a0001c0011t0001g0251 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.372-382C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704367 | |||||||
| chr14:51704371 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.372-378T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704371 | |||||||
| chr14:51704373 | T | C | 91 | a0001c0002t0001g0164 a0001c0003t0001g0005 a0001c0003t0001g0006 others(88): Show |
119 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.372-376T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704373 | |||||||
| chr14:51704570 | A | G | 35 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0002g0002 others(32): Show |
49 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.372-179A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704570 | |||||||
| chr14:51704691 | T | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.372-58T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704691 | |||||||
| chr14:51705008 | C | T | 29 | a0001c0002t0001g0008 a0001c0002t0001g0076 a0001c0002t0001g0077 others(26): Show |
40 | HG00597.hp2 HG00609.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.558+73C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705008 | |||||||
| chr14:51705034 | T | G | 2 | a0001c0002t0001g0149 a0001c0002t0001g0211 |
2 | HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.558+99T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705034 | |||||||
| chr14:51705188 | C | T | 1 | a0001c0003t0001g0256 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.558+253C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705188 | |||||||
| chr14:51705311 | C | G | 1 | a0001c0002t0002g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.558+376C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705311 | |||||||
| chr14:51705371 | C | G | 4 | a0001c0004t0001g0067 a0001c0004t0001g0069 a0001c0004t0001g0070 others(1): Show |
4 | HG00280.hp1 HG01167.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+436C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705371 | |||||||
| chr14:51705429 | C | T | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.558+494C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705429 | |||||||
| chr14:51705430 | G | A | 15 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0002g0014 others(12): Show |
19 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.558+495G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705430 | |||||||
| chr14:51705618 | A | G | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+683A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705618 | |||||||
| chr14:51705648 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.558+713A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705648 | |||||||
| chr14:51705793 | A | G | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.558+858A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705793 | |||||||
| chr14:51705923 | A | T | 1 | a0001c0002t0001g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.558+988A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705923 | |||||||
| chr14:51705981 | G | T | 188 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(185): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.558+1046G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705981 | |||||||
| chr14:51706025 | G | A | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.558+1090G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51706025 | |||||||
| chr14:51706163 | T | C | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1228T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51706163 | |||||||
| chr14:51706521 | T | G | 6 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0007g0119 others(3): Show |
6 | HG00733.hp2 HG01109.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.559-1557T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51706521 | |||||||
| chr14:51706780 | A | T | 9 | a0001c0002t0001g0194 a0001c0004t0001g0023 a0001c0004t0001g0050 others(6): Show |
10 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.559-1298A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51706780 | |||||||
| chr14:51706985 | T | C | 75 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(72): Show |
100 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.559-1093T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51706985 | |||||||
| chr14:51707027 | C | CT | 14 | a0001c0001t0002g0030 a0001c0001t0002g0051 a0001c0001t0002g0052 others(11): Show |
14 | HG00738.hp1 HG01168.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.559-1050dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 51707027 | ||||||
| chr14:51707660 | A | T | 206 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(203): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.559-418A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51707660 | |||||||
| chr14:51707761 | G | T | 1 | a0001c0003t0001g0267 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.559-317G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51707761 | |||||||
| chr14:51707805 | A | T | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.559-273A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51707805 | |||||||
| chr14:51707872 | C | T | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.559-206C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51707872 | |||||||
| chr14:51707959 | A | C | 9 | a0001c0004t0001g0039 a0001c0006t0003g0011 a0001c0006t0003g0075 others(6): Show |
12 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.559-119A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51707959 | |||||||
| chr14:51708243 | G | A | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.714+10G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708243 | |||||||
| chr14:51708329 | C | A | 192 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(189): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.714+96C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708329 | |||||||
| chr14:51708613 | A | C | 6 | a0001c0003t0001g0019 a0001c0003t0001g0224 a0001c0003t0001g0264 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.714+380A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708613 | |||||||
| chr14:51708715 | T | A | 8 | a0001c0002t0001g0194 a0001c0004t0001g0023 a0001c0004t0001g0050 others(5): Show |
9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.714+482T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708715 | |||||||
| chr14:51708763 | T | A | 83 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(80): Show |
110 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.714+530T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708763 | |||||||
| chr14:51708956 | C | T | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+723C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708956 | |||||||
| chr14:51709134 | G | A | 74 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(71): Show |
98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.714+901G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709134 | |||||||
| chr14:51709359 | G | A | 1 | a0001c0004t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.714+1126G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709359 | |||||||
| chr14:51709363 | C | A | 1 | a0001c0003t0001g0049 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.714+1130C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709363 | |||||||
| chr14:51709564 | A | G | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0007t0001g0057 others(1): Show |
4 | HG02630.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1331A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709564 | |||||||
| chr14:51709655 | C | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+1422C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709655 | |||||||
| chr14:51709715 | A | G | 1 | a0001c0003t0001g0266 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.714+1482A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709715 | |||||||
| chr14:51709859 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.714+1626C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709859 | |||||||
| chr14:51709893 | G | T | 10 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(7): Show |
11 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1638G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709893 | |||||||
| chr14:51709894 | A | T | 10 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(7): Show |
11 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1637A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709894 | |||||||
| chr14:51709913 | A | T | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1618A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709913 | |||||||
| chr14:51709950 | T | C | 1 | a0003c0010t0001g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.715-1581T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709950 | |||||||
| chr14:51710045 | G | A | 9 | a0001c0001t0002g0030 a0001c0001t0002g0051 a0001c0001t0002g0144 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-1486G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710045 | |||||||
| chr14:51710156 | G | A | 8 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(5): Show |
9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-1375G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710156 | |||||||
| chr14:51710222 | T | C | 8 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0036 others(5): Show |
11 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1309T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710222 | |||||||
| chr14:51710270 | A | C | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.715-1261A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710270 | |||||||
| chr14:51710310 | G | A | 9 | a0001c0001t0002g0030 a0001c0001t0002g0051 a0001c0001t0002g0144 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-1221G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710310 | |||||||
| chr14:51710402 | C | T | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.715-1129C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710402 | |||||||
| chr14:51710455 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.715-1076T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710455 | |||||||
| chr14:51710697 | C | G | 1 | a0001c0001t0002g0108 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.715-834C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710697 | |||||||
| chr14:51710809 | G | A | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.715-722G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710809 | |||||||
| chr14:51710871 | A | G | 104 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(101): Show |
130 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.715-660A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710871 | |||||||
| chr14:51711177 | AAATC | A | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.715-351_715-348del others(4): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr14 | 51711177 | ||||||
| chr14:51711253 | A | C | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.715-278A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51711253 | |||||||
| chr14:51711320 | G | C | 104 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(101): Show |
130 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.715-211G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51711320 | |||||||
| chr14:51711360 | T | G | 10 | a0001c0001t0001g0111 a0001c0001t0002g0058 a0001c0001t0002g0112 others(7): Show |
10 | HG01891.hp1 HG02486.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-171T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51711360 | |||||||
| chr14:51711444 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.715-87C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51711444 | |||||||
| chr14:51711902 | G | A | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+306G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 8/13 | chr14 | 51711902 | |||||||
| chr14:51712173 | A | C | 105 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(102): Show |
131 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.781-310A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 8/13 | chr14 | 51712173 | |||||||
| chr14:51712268 | C | T | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.781-215C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 8/13 | chr14 | 51712268 | |||||||
| chr14:51712341 | T | C | 105 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(102): Show |
132 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.781-142T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 8/13 | chr14 | 51712341 | |||||||
| chr14:51712733 | T | G | 208 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(205): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.849+182T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51712733 | |||||||
| chr14:51712874 | G | A | 2 | a0001c0003t0001g0013 a0001c0003t0001g0038 |
5 | HG02818.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+323G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51712874 | |||||||
| chr14:51713080 | G | A | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.849+529G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713080 | |||||||
| chr14:51713083 | T | C | 75 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(72): Show |
100 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.849+532T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713083 | |||||||
| chr14:51713106 | G | GT | 5 | a0001c0001t0002g0022 a0001c0001t0002g0065 a0001c0001t0002g0066 others(2): Show |
6 | HG00099.hp2 HG01516.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+561dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 51713106 | ||||||
| chr14:51713178 | C | T | 1 | a0001c0002t0001g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.849+627C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713178 | |||||||
| chr14:51713235 | A | G | 1 | a0001c0001t0002g0227 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.849+684A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713235 | |||||||
| chr14:51713382 | C | T | 1 | a0001c0003t0001g0252 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.849+831C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713382 | |||||||
| chr14:51713458 | CA | C | 186 | a0001c0001t0001g0111 a0001c0001t0001g0166 a0001c0001t0001g0198 others(183): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.849+926delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 51713458 | ||||||
| chr14:51713480 | G | A | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.849+929G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713480 | |||||||
| chr14:51713520 | GA | G | 5 | a0001c0001t0002g0022 a0001c0001t0002g0065 a0001c0001t0002g0066 others(2): Show |
6 | HG00099.hp2 HG01516.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+970delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713520 | |||||||
| chr14:51713602 | C | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0112 |
2 | HG01891.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.849+1051C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713602 | |||||||
| chr14:51713729 | A | G | 6 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0158 others(3): Show |
6 | HG02886.hp2 HG02922.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+1178A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713729 | |||||||
| chr14:51713757 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.849+1206A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713757 | |||||||
| chr14:51713990 | C | A | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.850-1335C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713990 | |||||||
| chr14:51714008 | G | C | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.850-1317G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714008 | |||||||
| chr14:51714268 | A | T | 101 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(98): Show |
127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.850-1057A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714268 | |||||||
| chr14:51714316 | T | G | 1 | a0001c0001t0002g0115 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.850-1009T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714316 | |||||||
| chr14:51714317 | TA | T | 101 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(98): Show |
127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.850-998delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 51714317 | ||||||
| chr14:51714327 | A | G | 101 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(98): Show |
127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.850-998A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714327 | |||||||
| chr14:51714381 | A | G | 10 | a0001c0004t0001g0039 a0001c0004t0016g0072 a0001c0006t0003g0011 others(7): Show |
13 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.850-944A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714381 | |||||||
| chr14:51714650 | A | C | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.850-675A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714650 | |||||||
| chr14:51714750 | T | C | 1 | a0001c0003t0001g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.850-575T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714750 | |||||||
| chr14:51714865 | A | G | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.850-460A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714865 | |||||||
| chr14:51714909 | G | A | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.850-416G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714909 | |||||||
| chr14:51715046 | C | T | 72 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(69): Show |
97 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.850-279C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51715046 | |||||||
| chr14:51715080 | G | C | 2 | a0001c0001t0002g0199 a0001c0001t0002g0207 |
2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.850-245G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51715080 | |||||||
| chr14:51715192 | C | T | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-133C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51715192 | |||||||
| chr14:51715219 | A | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-106A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51715219 | |||||||
| chr14:51715607 | A | G | 1 | a0001c0002t0001g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1024+108A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51715607 | |||||||
| chr14:51715688 | T | C | 201 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(198): Show |
256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1024+189T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51715688 | |||||||
| chr14:51715761 | A | T | 1 | a0001c0001t0002g0300 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1024+262A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51715761 | |||||||
| chr14:51715783 | C | CA | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+289dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 51715783 | ||||||
| chr14:51715850 | A | T | 68 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(65): Show |
93 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1024+351A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51715850 | |||||||
| chr14:51716124 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1024+625C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716124 | |||||||
| chr14:51716296 | G | T | 1 | a0001c0002t0002g0220 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1024+797G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716296 | |||||||
| chr14:51716599 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1024+1100A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716599 | |||||||
| chr14:51716687 | T | G | 1 | a0001c0001t0002g0226 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1024+1188T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716687 | |||||||
| chr14:51716887 | C | G | 199 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(196): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1024+1388C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716887 | |||||||
| chr14:51716929 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1024+1430C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716929 | |||||||
| chr14:51717025 | C | G | 1 | a0001c0002t0001g0194 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1024+1526C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717025 | |||||||
| chr14:51717168 | G | A | 2 | a0001c0001t0011g0130 a0001c0001t0011g0131 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1024+1669G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717168 | |||||||
| chr14:51717172 | CTTTG | C | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1681_1024+168 others(8): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 51717172 | ||||||
| chr14:51717187 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1024+1688G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717187 | |||||||
| chr14:51717271 | G | A | 1 | a0001c0003t0001g0283 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1024+1772G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717271 | |||||||
| chr14:51717359 | G | A | 2 | a0001c0001t0002g0014 a0005c0012t0002g0206 |
4 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1860G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717359 | |||||||
| chr14:51717379 | G | A | 71 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(68): Show |
93 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1024+1880G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717379 | |||||||
| chr14:51717440 | C | G | 1 | a0001c0003t0001g0270 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1024+1941C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717440 | |||||||
| chr14:51717516 | A | G | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1024+2017A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717516 | |||||||
| chr14:51717655 | G | A | 1 | a0001c0003t0001g0274 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1024+2156G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717655 | |||||||
| chr14:51717710 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1024+2211A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717710 | |||||||
| chr14:51717721 | C | G | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1024+2222C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717721 | |||||||
| chr14:51717882 | C | A | 8 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(5): Show |
9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025-2173C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717882 | |||||||
| chr14:51717888 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1025-2167G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717888 | |||||||
| chr14:51718106 | C | T | 1 | a0001c0003t0001g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1025-1949C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718106 | |||||||
| chr14:51718139 | G | A | 4 | a0001c0003t0001g0017 a0001c0003t0001g0249 a0001c0003t0001g0256 others(1): Show |
6 | HG01081.hp2 HG01106.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1025-1916G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718139 | |||||||
| chr14:51718266 | G | A | 101 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(98): Show |
127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1025-1789G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718266 | |||||||
| chr14:51718352 | A | G | 1 | a0001c0002t0001g0223 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1025-1703A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718352 | |||||||
| chr14:51718421 | G | A | 205 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(202): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1025-1634G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718421 | |||||||
| chr14:51718487 | T | G | 2 | a0001c0007t0001g0057 a0001c0007t0001g0099 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1025-1568T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718487 | |||||||
| chr14:51718825 | A | G | 1 | a0001c0013t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1025-1230A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718825 | |||||||
| chr14:51719068 | T | A | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1025-987T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719068 | |||||||
| chr14:51719117 | C | T | 2 | a0001c0002t0001g0037 a0001c0002t0001g0196 |
3 | HG02809.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1025-938C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719117 | |||||||
| chr14:51719170 | G | A | 8 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(5): Show |
9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025-885G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719170 | |||||||
| chr14:51719228 | A | AG | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1025-827_1025-826i others(3): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719228 | |||||||
| chr14:51719554 | A | G | 2 | a0001c0003t0001g0217 a0001c0003t0001g0225 |
2 | HG01192.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1025-501A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719554 | |||||||
| chr14:51719619 | G | T | 1 | a0001c0003t0001g0249 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1025-436G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719619 | |||||||
| chr14:51719682 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1025-373G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719682 | |||||||
| chr14:51719697 | A | G | 1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1025-358A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719697 | |||||||
| chr14:51719756 | A | G | 3 | a0001c0002t0001g0047 a0001c0002t0001g0061 a0001c0004t0012g0180 |
4 | HG01496.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025-299A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719756 | |||||||
| chr14:51719848 | T | C | 1 | a0001c0003t0001g0255 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1025-207T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719848 | |||||||
| chr14:51720011 | G | A | 3 | a0001c0001t0011g0130 a0001c0001t0011g0131 a0001c0001t0024g0123 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1025-44G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51720011 | |||||||
| chr14:51720050 | C | T | 1 | a0001c0003t0001g0260 | 1 | NA19079.hp2 | splice_region_variant&intron_variant | LOW | c.1025-5C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51720050 | |||||||
| chr14:51720555 | G | A | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1360+165G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720555 | |||||||
| chr14:51720775 | C | T | 1 | a0001c0003t0001g0265 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1360+385C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720775 | |||||||
| chr14:51720851 | A | T | 1 | a0001c0001t0002g0106 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1360+461A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720851 | |||||||
| chr14:51720914 | A | G | 1 | a0001c0003t0001g0270 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1360+524A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720914 | |||||||
| chr14:51720917 | A | G | 1 | a0001c0002t0001g0088 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1360+527A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720917 | |||||||
| chr14:51720932 | C | T | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1360+542C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720932 | |||||||
| chr14:51721267 | G | T | 102 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(99): Show |
128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.1361-682G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721267 | |||||||
| chr14:51721285 | A | ATAATCTT others(10): Show |
1 | a0001c0001t0002g0304 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1361-664_1361-663i others(19): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721285 | |||||||
| chr14:51721288 | C | A | 1 | a0001c0001t0002g0304 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1361-661C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721288 | |||||||
| chr14:51721311 | C | T | 2 | a0001c0001t0002g0014 a0005c0012t0002g0206 |
4 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-638C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721311 | |||||||
| chr14:51721388 | G | A | 8 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(5): Show |
10 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1361-561G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721388 | |||||||
| chr14:51721409 | A | G | 1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1361-540A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721409 | |||||||
| chr14:51721426 | A | G | 106 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(103): Show |
132 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1361-523A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721426 | |||||||
| chr14:51721481 | G | C | 4 | a0001c0001t0001g0111 a0001c0001t0002g0058 a0001c0001t0002g0112 others(1): Show |
4 | HG01891.hp1 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-468G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721481 | |||||||
| chr14:51721488 | C | T | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1361-461C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721488 | |||||||
| chr14:51721645 | GGGAA | G | 208 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(205): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1361-287_1361-284d others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721645 | ||||||
| chr14:51721692 | CAGGAAGG others(1): Show |
C | 75 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(72): Show |
101 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1361-237_1361-230d others(10): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721692 | ||||||
| chr14:51721696 | A | AAGGAAGG others(69): Show |
6 | a0001c0006t0003g0011 a0001c0006t0003g0075 a0001c0006t0003g0150 others(3): Show |
8 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1361-234_1361-233i others(78): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721696 | ||||||
| chr14:51721696 | A | AAGGAAGG others(69): Show |
1 | a0001c0006t0003g0151 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1361-234_1361-233i others(78): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721696 | ||||||
| chr14:51721700 | A | AAGGAAGG others(69): Show |
1 | a0001c0004t0016g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1361-234_1361-233i others(78): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721700 | ||||||
| chr14:51721708 | A | AAGGG | 15 | a0001c0002t0001g0194 a0001c0003t0001g0192 a0001c0004t0001g0023 others(12): Show |
16 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1361-238_1361-237i others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721708 | ||||||
| chr14:51721709 | A | AGGAAGGG others(57): Show |
1 | a0001c0006t0022g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1361-234_1361-233i others(66): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721709 | ||||||
| chr14:51721712 | A | G | 106 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(103): Show |
132 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1361-237A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721712 | |||||||
| chr14:51721720 | G | A | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1361-229G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721720 | |||||||
| chr14:51721732 | G | A | 120 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(117): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1361-217G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721732 | |||||||
| chr14:51721744 | A | G | 1 | a0001c0004t0005g0184 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1361-205A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721744 | |||||||
| chr14:51721745 | A | AGGAGGGA others(61): Show |
1 | a0001c0004t0001g0023 | 2 | HG01243.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1361-202_1361-201i others(70): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721745 | ||||||
| chr14:51721745 | A | AGGAGGGA others(69): Show |
7 | a0001c0002t0001g0194 a0001c0004t0001g0050 a0001c0004t0001g0067 others(4): Show |
7 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-202_1361-201i others(78): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721745 | ||||||
| chr14:51721745 | A | AGGAGGGA others(33): Show |
2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1361-202_1361-201i others(42): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721745 | ||||||
| chr14:51721745 | A | AGGAGGGA others(41): Show |
4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp1 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-202_1361-201i others(50): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721745 | ||||||
| chr14:51721745 | A | AGGAGGGA others(49): Show |
1 | a0001c0004t0001g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1361-202_1361-201i others(58): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721745 | ||||||
| chr14:51721748 | G | A | 19 | a0001c0002t0001g0126 a0001c0002t0001g0194 a0001c0003t0001g0192 others(16): Show |
20 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1361-201G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721748 | |||||||
| chr14:51721749 | A | G | 2 | a0001c0003t0001g0192 a0003c0010t0001g0073 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1361-200A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721749 | |||||||
| chr14:51721753 | A | AGGAACAA others(177): Show |
1 | a0001c0002t0001g0126 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1361-192_1361-191i others(186): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | ||||||
| chr14:51721753 | A | AGGAAGGA others(1): Show |
94 | a0001c0002t0001g0003 a0001c0002t0001g0008 a0001c0002t0001g0015 others(91): Show |
121 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1361-179_1361-172d others(10): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | ||||||
| chr14:51721753 | A | AGGAAGGA others(105): Show |
1 | a0001c0002t0001g0258 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1361-172_1361-171i others(114): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | ||||||
| chr14:51721753 | A | AGGAAGGA others(22): Show |
9 | a0001c0004t0001g0039 a0001c0004t0016g0072 a0001c0006t0003g0011 others(6): Show |
12 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1361-182_1361-181i others(31): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | ||||||
| chr14:51721753 | A | AGGAAGGA others(30): Show |
1 | a0001c0006t0022g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1361-182_1361-181i others(39): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | ||||||
| chr14:51721753 | A | AGGAAGGA others(139): Show |
3 | a0001c0004t0005g0183 a0001c0004t0005g0188 a0001c0004t0005g0282 |
3 | NA18994.hp2 NA19055.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1361-182_1361-181i others(148): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | ||||||
| chr14:51721753 | A | AGGAAGGG others(151): Show |
1 | a0001c0004t0005g0184 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1361-190_1361-189i others(160): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | ||||||
| chr14:51721753 | A | AGGAGGGA others(13): Show |
4 | a0001c0001t0002g0145 a0001c0001t0002g0147 a0001c0001t0002g0284 others(1): Show |
4 | HG02280.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-193_1361-192i others(22): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | ||||||
| chr14:51721753 | A | AGGAGGGA others(21): Show |
98 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(95): Show |
124 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1361-193_1361-192i others(30): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | ||||||
| chr14:51721753 | A | AGGAGGGA others(29): Show |
1 | a0001c0004t0012g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1361-193_1361-192i others(38): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | ||||||
| chr14:51721753 | A | G | 15 | a0001c0002t0001g0194 a0001c0004t0001g0023 a0001c0004t0001g0050 others(12): Show |
16 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1361-196A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721753 | |||||||
| chr14:51721759 | G | GAGGGA | 75 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0013 others(72): Show |
101 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1361-186_1361-182d others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721759 | ||||||
| chr14:51721761 | G | A | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1361-188G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721761 | |||||||
| chr14:51721777 | G | C | 1 | a0001c0003t0001g0269 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1361-172G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721777 | |||||||
| chr14:51722333 | G | A | 1 | a0001c0003t0001g0045 | 2 | NA19002.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1492+253G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51722333 | |||||||
| chr14:51722482 | G | A | 1 | a0001c0002t0008g0018 | 3 | NA18957.hp2 NA18961.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1492+402G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51722482 | |||||||
| chr14:51722604 | T | G | 1 | a0001c0015t0001g0237 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1492+524T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51722604 | |||||||
| chr14:51722697 | C | T | 1 | a0001c0003t0001g0016 | 3 | HG00735.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1492+617C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51722697 | |||||||
| chr14:51723018 | C | T | 2 | a0002c0008t0009g0074 a0002c0008t0009g0281 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1492+938C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723018 | |||||||
| chr14:51723023 | C | T | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+943C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723023 | |||||||
| chr14:51723071 | G | A | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+991G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723071 | |||||||
| chr14:51723304 | A | G | 2 | a0001c0001t0002g0159 a0001c0001t0002g0160 |
2 | NA18942.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1492+1224A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723304 | |||||||
| chr14:51723504 | G | T | 4 | a0001c0004t0001g0141 a0001c0004t0001g0142 a0001c0004t0001g0203 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1492+1424G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723504 | |||||||
| chr14:51723623 | T | A | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1543T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723623 | |||||||
| chr14:51723624 | G | T | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1544G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723624 | |||||||
| chr14:51723625 | C | A | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1545C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723625 | |||||||
| chr14:51723625 | C | CA | 6 | a0001c0002t0001g0043 a0001c0002t0001g0087 a0001c0002t0001g0092 others(3): Show |
7 | NA18954.hp1 NA18978.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.1492+1557dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51723625 | ||||||
| chr14:51723626 | A | C | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1546A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723626 | |||||||
| chr14:51723633 | A | G | 1 | a0001c0002t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1492+1553A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723633 | |||||||
| chr14:51723660 | A | T | 1 | a0001c0001t0002g0304 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1492+1580A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723660 | |||||||
| chr14:51723721 | C | G | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1641C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723721 | |||||||
| chr14:51723731 | T | C | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1651T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723731 | |||||||
| chr14:51723772 | C | CA | 109 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(106): Show |
137 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1492+1706dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51723772 | ||||||
| chr14:51723772 | CA | C | 95 | a0001c0002t0001g0232 a0001c0002t0001g0241 a0001c0003t0001g0005 others(92): Show |
122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1492+1706delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51723772 | ||||||
| chr14:51723803 | T | C | 1 | a0001c0003t0001g0192 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1492+1723T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723803 | |||||||
| chr14:51723847 | C | T | 12 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(9): Show |
13 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1492+1767C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723847 | |||||||
| chr14:51723876 | A | T | 12 | a0001c0004t0001g0023 a0001c0004t0001g0050 a0001c0004t0001g0067 others(9): Show |
13 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1492+1796A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723876 | |||||||
| chr14:51723935 | A | G | 4 | a0001c0002t0001g0033 a0001c0002t0001g0177 a0001c0002t0001g0178 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1493-1844A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723935 | |||||||
| chr14:51723957 | A | G | 1 | a0001c0002t0002g0200 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1493-1822A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723957 | |||||||
| chr14:51724063 | A | G | 4 | a0001c0002t0001g0033 a0001c0002t0001g0177 a0001c0002t0001g0178 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1493-1716A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724063 | |||||||
| chr14:51724097 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1493-1682A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724097 | |||||||
| chr14:51724106 | C | A | 1 | a0001c0001t0002g0154 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1493-1673C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724106 | |||||||
| chr14:51724141 | A | C | 1 | a0004c0016t0002g0104 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1493-1638A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724141 | |||||||
| chr14:51724209 | T | TA | 6 | a0001c0001t0002g0107 a0001c0001t0002g0155 a0001c0002t0001g0076 others(3): Show |
6 | HG03688.hp1 NA18961.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1493-1556dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51724209 | ||||||
| chr14:51724209 | TA | T | 4 | a0001c0001t0002g0304 a0001c0003t0001g0017 a0001c0003t0001g0256 others(1): Show |
6 | HG01081.hp2 HG01106.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1493-1556delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51724209 | ||||||
| chr14:51724374 | A | C | 3 | a0001c0003t0001g0137 a0001c0003t0001g0268 a0001c0003t0001g0287 |
3 | NA18941.hp1 NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1493-1405A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724374 | |||||||
| chr14:51724731 | G | GT | 79 | a0001c0001t0001g0111 a0001c0002t0001g0164 a0001c0003t0001g0005 others(76): Show |
105 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1493-1036dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51724731 | ||||||
| chr14:51724763 | T | C | 76 | a0001c0002t0001g0164 a0001c0003t0001g0005 a0001c0003t0001g0006 others(73): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1493-1016T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724763 | |||||||
| chr14:51724941 | C | G | 1 | a0001c0001t0024g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1493-838C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724941 | |||||||
| chr14:51724972 | A | G | 4 | a0001c0004t0005g0183 a0001c0004t0005g0184 a0001c0004t0005g0188 others(1): Show |
4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1493-807A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724972 | |||||||
| chr14:51725581 | A | G | 2 | a0001c0002t0001g0149 a0001c0002t0001g0211 |
2 | HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1493-198A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51725581 | |||||||
| chr14:51725766 | T | G | 1 | a0001c0001t0002g0168 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1493-13T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51725766 | |||||||
| chr14:51726047 | T | C | 3 | a0001c0001t0006g0021 a0001c0001t0006g0063 a0001c0001t0023g0062 |
4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1584+177T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51726047 | |||||||
| chr14:51726074 | T | C | 103 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0166 others(100): Show |
129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1584+204T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51726074 | |||||||
| chr14:51726085 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1584+215T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51726085 | |||||||
| chr14:51726695 | C | T | 3 | a0001c0001t0011g0130 a0001c0001t0011g0131 a0001c0001t0024g0123 |
3 | HG02896.hp2 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1584+825C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51726695 | |||||||
| chr14:51726842 | C | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0112 |
2 | HG01891.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1585-903C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51726842 | |||||||
| chr14:51727021 | G | C | 1 | a0001c0002t0002g0200 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1585-724G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727021 | |||||||
| chr14:51727027 | T | TA | 8 | a0001c0006t0003g0011 a0001c0006t0003g0150 a0001c0006t0003g0151 others(5): Show |
10 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1585-710dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 51727027 | ||||||
| chr14:51727027 | TA | T | 18 | a0001c0001t0002g0103 a0001c0003t0001g0006 a0001c0003t0001g0019 others(15): Show |
25 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1585-710delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 51727027 | ||||||
| chr14:51727042 | C | T | 1 | a0001c0004t0001g0039 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1585-703C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727042 | |||||||
| chr14:51727083 | G | A | 1 | a0001c0003t0001g0271 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1585-662G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727083 | |||||||
| chr14:51727094 | G | A | 5 | a0001c0001t0002g0022 a0001c0001t0002g0053 a0001c0001t0002g0156 others(2): Show |
6 | HG00099.hp2 HG00639.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1585-651G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727094 | |||||||
| chr14:51727309 | G | GA | 96 | a0001c0001t0001g0111 a0001c0001t0002g0001 a0001c0001t0002g0002 others(93): Show |
122 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1585-425dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 51727309 | ||||||
| chr14:51727489 | G | A | 101 | a0001c0001t0001g0111 a0001c0001t0002g0001 a0001c0001t0002g0002 others(98): Show |
127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1585-256G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727489 | |||||||
| chr14:51727689 | G | A | 101 | a0001c0001t0001g0111 a0001c0001t0002g0001 a0001c0001t0002g0002 others(98): Show |
127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1585-56G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727689 |