Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54842 |
| ensemblid | ENSG00000151690.15 |
| hgncid | 24711 |
| symbol | MFSD6 |
| name | major facilitator superfamily domain containing 6 |
| refseq_nuc | NM_017694.4 |
| refseq_prot | NP_060164.3 |
| ensembl_nuc | ENST00000392328.6 |
| ensembl_prot | ENSP00000376141.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 190408355 |
| end | 190502314 |
| strand | + |
| ver | v1.2 |
| region | chr2:190408355-190502314 |
| region5000 | chr2:190403355-190507314 |
| regionname0 | MFSD6_chr2_190408355_190502314 |
| regionname5000 | MFSD6_chr2_190403355_190507314 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 791 | 177 | 44 | 26 | 79 | 9 | 18 | 61 | MFSD6_chr2_190403355_190507314 | MFSD6 | MADDK others(786): Show |
chr2 | 190403355 | 190507314 |
| a0002 | 0/1 | 791 | 157 | 21 | 29 | 93 | 3 | 10 | 75 | MFSD6_chr2_190403355_190507314 | MFSD6 | MADDK others(786): Show |
chr2 | 190403355 | 190507314 |
| a0003 | 0/0 | 791 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | MADDK others(786): Show |
chr2 | 190403355 | 190507314 |
| a0004 | 0/0 | 791 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | MADDK others(786): Show |
chr2 | 190403355 | 190507314 |
| a0005 | 0/0 | 791 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MFSD6_chr2_190403355_190507314 | MFSD6 | MADDK others(786): Show |
chr2 | 190403355 | 190507314 |
| a0006 | 0/0 | 791 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | MADDK others(786): Show |
chr2 | 190403355 | 190507314 |
| a0007 | 0/0 | 791 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | MADDK others(786): Show |
chr2 | 190403355 | 190507314 |
| a0008 | 0/0 | 791 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | MADDK others(786): Show |
chr2 | 190403355 | 190507314 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2373 | 175 | 43 | 26 | 78 | 9 | 18 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 | ||
| a0001c0007 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 | ||
| a0001c0010 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 | ||
| a0002c0002 | 0/1 | 2373 | 156 | 20 | 29 | 93 | 3 | 10 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 | ||
| a0002c0011 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 | ||
| a0003c0003 | 0/0 | 2373 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 | ||
| a0004c0004 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 | ||
| a0005c0005 | 0/0 | 2373 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 | ||
| a0006c0008 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 | ||
| a0007c0006 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 | ||
| a0008c0009 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | ATGGC others(2368): Show |
chr2 | 190403355 | 190507314 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4796 | 29 | 19 | 4 | 1 | 2 | 3 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0002 | 0/0 | 4796 | 80 | 17 | 9 | 47 | 2 | 5 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0003 | 0/0 | 4796 | 47 | 0 | 13 | 21 | 4 | 9 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0006 | 0/0 | 4796 | 4 | 0 | 0 | 4 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0007 | 0/0 | 4795 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4790): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0008 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0011 | 0/0 | 4796 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0012 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0014 | 1/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0016 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0017 | 0/0 | 4782 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4777): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0018 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0020 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0021 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0001t0023 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0007t0001 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0001c0010t0002 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0002c0002t0001 | 0/1 | 4796 | 136 | 13 | 23 | 89 | 3 | 7 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0002c0002t0003 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0002c0002t0004 | 0/0 | 4796 | 6 | 0 | 5 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0002c0002t0005 | 0/0 | 4796 | 5 | 5 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0002c0002t0008 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0002c0002t0009 | 0/0 | 4796 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0002c0002t0013 | 0/0 | 4796 | 2 | 0 | 1 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0002c0002t0019 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0002c0011t0001 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0003c0003t0010 | 0/0 | 4794 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4789): Show |
chr2 | 190403355 | 190507314 |
| a0003c0003t0022 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4789): Show |
chr2 | 190403355 | 190507314 |
| a0004c0004t0001 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0005c0005t0001 | 0/0 | 4796 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0006c0008t0003 | 0/0 | 4796 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0007c0006t0001 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| a0008c0009t0015 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | GTCGC others(4791): Show |
chr2 | 190403355 | 190507314 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0006g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0006g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0008g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0011g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0012g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0014g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0016g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0017g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0018g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0020g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0021g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0001t0023g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0007t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0001c0010t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0306 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0009g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0009g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0009g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0013g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0013g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0002t0019g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0002c0011t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0003c0003t0010g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0003c0003t0010g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0003c0003t0022g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0004c0004t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0004c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0005c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0005c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0006c0008t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0007c0006t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| a0008c0009t0015g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0153 | EUR | GBR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | GBR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00323 | hp1 | a0001 | c0001 | t0016 | g0114 | EUR | FIN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0029 | EUR | FIN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00408 | hp2 | a0001 | c0001 | t0011 | g0037 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00639 | hp2 | a0002 | c0002 | t0013 | g0302 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0286 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01070 | hp2 | a0002 | c0002 | t0004 | g0163 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01071 | hp1 | a0002 | c0002 | t0004 | g0154 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01074 | hp1 | a0006 | c0008 | t0003 | g0028 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0307 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0269 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01256 | hp2 | a0002 | c0002 | t0004 | g0006 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0294 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01258 | hp2 | a0002 | c0002 | t0004 | g0006 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0259 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0117 | EUR | IBS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | IBS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0017 | EUR | IBS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | IBS | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01884 | hp2 | a0002 | c0011 | t0001 | g0320 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0266 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0303 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0152 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02015 | hp2 | a0001 | c0001 | t0018 | g0054 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0329 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02074 | hp2 | a0002 | c0002 | t0009 | g0305 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0247 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CDX | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | CDX | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02258 | hp2 | a0002 | c0002 | t0005 | g0200 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02280 | hp1 | a0002 | c0002 | t0005 | g0218 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0289 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PEL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0319 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | KHV | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0142 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02647 | hp1 | a0002 | c0002 | t0005 | g0205 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02818 | hp1 | a0001 | c0001 | t0021 | g0210 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0322 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0321 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03098 | hp1 | a0002 | c0002 | t0005 | g0187 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03195 | hp2 | a0003 | c0003 | t0022 | g0207 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0188 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03225 | hp1 | a0002 | c0002 | t0005 | g0149 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03239 | hp2 | a0002 | c0002 | t0013 | g0314 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03453 | hp1 | a0003 | c0003 | t0010 | g0331 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0203 | AFR | ESN | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03579 | hp1 | a0003 | c0003 | t0010 | g0330 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03654 | hp1 | a0002 | c0002 | t0004 | g0214 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0282 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03669 | hp1 | a0002 | c0002 | t0003 | g0066 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0300 | SAS | PJL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0217 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0287 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | BEB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0276 | SAS | STU | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | STU | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG04228 | hp1 | a0001 | c0001 | t0020 | g0248 | SAS | STU | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | STU | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18522 | hp1 | a0008 | c0009 | t0015 | g0208 | AFR | YRI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18522 | hp2 | a0002 | c0002 | t0008 | g0202 | AFR | YRI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | CHB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CHB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | YRI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0236 | AFR | YRI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18957 | hp2 | a0002 | c0002 | t0009 | g0296 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18963 | hp2 | a0001 | c0001 | t0017 | g0044 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18977 | hp1 | a0005 | c0005 | t0001 | g0272 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18986 | hp1 | a0001 | c0007 | t0001 | g0035 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18992 | hp1 | a0001 | c0001 | t0011 | g0043 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18993 | hp2 | a0001 | c0001 | t0023 | g0041 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19004 | hp2 | a0002 | c0002 | t0009 | g0317 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19007 | hp2 | a0005 | c0005 | t0001 | g0284 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19030 | hp2 | a0001 | c0010 | t0002 | g0098 | AFR | LWK | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19078 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19089 | hp1 | a0002 | c0002 | t0019 | g0295 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0024 | EUR | TSI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | TSI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01123 | hp1 | a0002 | c0002 | t0004 | g0213 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0219 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02559 | hp1 | a0007 | c0006 | t0001 | g0324 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03471 | hp1 | a0002 | c0002 | t0008 | g0211 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0332 | AFR | USA | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA21309 | hp1 | a0004 | c0004 | t0001 | g0323 | AFR | LWK | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | LWK | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0306 | REF | REF | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0014 | g0209 | REF | REF | MFSD6_chr2_190403355_190507314 | MFSD6 | chr2 | 190403355 | 190507314 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190436190 | T | C | 2 | a0004 a0007 |
3 | HG02559.hp1 HG02970.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.161T>C | p.Ile54Thr | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 485/4796 | 161/2376 | 54/791 | chr2 | 190436190 | |||
| chr2:190436567 | C | T | 1 | a0008 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.538C>T | p.Pro180Ser | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 862/4796 | 538/2376 | 180/791 | chr2 | 190436567 | |||
| chr2:190436597 | A | T | 1 | a0003 | 3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.568A>T | p.Thr190Ser | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 892/4796 | 568/2376 | 190/791 | chr2 | 190436597 | |||
| chr2:190436642 | A | G | 4 | a0002 a0004 a0005 others(1): Show |
161 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(158): Show |
missense_variant | MODERATE | c.613A>G | p.Arg205Gly | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 937/4796 | 613/2376 | 205/791 | chr2 | 190436642 | |||
| chr2:190436709 | A | C | 1 | a0007 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.680A>C | p.Gln227Pro | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 1004/4796 | 680/2376 | 227/791 | chr2 | 190436709 | |||
| chr2:190436768 | G | A | 1 | a0005 | 2 | NA18977.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.739G>A | p.Ala247Thr | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 1063/4796 | 739/2376 | 247/791 | chr2 | 190436768 | |||
| chr2:190500102 | C | T | 1 | a0006 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.2260C>T | p.Pro754Ser | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 2584/4796 | 2260/2376 | 754/791 | chr2 | 190500102 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190436119 | C | T | 1 | a0002c0011 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.90C>T | p.Ser30Ser | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 414/4796 | 90/2376 | 30/791 | chr2 | 190436119 | |||
| chr2:190436227 | C | T | 1 | a0001c0010 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.198C>T | p.Asn66Asn | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 522/4796 | 198/2376 | 66/791 | chr2 | 190436227 | |||
| chr2:190436566 | G | T | 1 | a0008c0009 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.537G>T | p.Leu179Leu | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/8 | 861/4796 | 537/2376 | 179/791 | chr2 | 190436566 | |||
| chr2:190500137 | C | T | 1 | a0001c0007 | 1 | NA18986.hp1 | synonymous_variant | LOW | c.2295C>T | p.Thr765Thr | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 2619/4796 | 2295/2376 | 765/791 | chr2 | 190500137 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190408382 | A | G | 1 | a0001c0001t0023 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-297A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/8 | 27648 | chr2 | 190408382 | ||||||
| chr2:190408424 | C | G | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
339 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(336): Show |
5_prime_UTR_variant | MODIFIER | c.-255C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/8 | 27606 | chr2 | 190408424 | ||||||
| chr2:190415331 | C | T | 1 | a0002c0002t0013 | 2 | HG00639.hp2 HG03239.hp2 |
5_prime_UTR_variant | MODIFIER | c.-136C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/8 | 20699 | chr2 | 190415331 | ||||||
| chr2:190415332 | G | A | 1 | a0001c0001t0016 | 1 | HG00323.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-135G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/8 | chr2 | 190415332 | |||||||
| chr2:190500317 | A | G | 1 | a0002c0002t0004 | 6 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*99A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 99 | chr2 | 190500317 | ||||||
| chr2:190500397 | G | A | 7 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0017 others(4): Show |
55 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*179G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 179 | chr2 | 190500397 | ||||||
| chr2:190500504 | GC | G | 1 | a0001c0001t0007 | 3 | HG02630.hp2 HG03453.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*288delC | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 288 | INFO_REALIGN_3_PRIME | chr2 | 190500504 | |||||
| chr2:190500568 | G | A | 1 | a0002c0002t0005 | 5 | HG02258.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*350G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 350 | chr2 | 190500568 | ||||||
| chr2:190500736 | T | C | 1 | a0001c0001t0006 | 4 | NA18982.hp1 NA19002.hp1 NA19007.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*518T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 518 | chr2 | 190500736 | ||||||
| chr2:190500964 | ATTTCAAA others(17): Show |
A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*748_*771delTTCAAA others(18): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 748 | INFO_REALIGN_3_PRIME | chr2 | 190500964 | |||||
| chr2:190501020 | A | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 802 | chr2 | 190501020 | ||||||
| chr2:190501021 | A | G | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*803A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 803 | chr2 | 190501021 | ||||||
| chr2:190501026 | A | G | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 808 | chr2 | 190501026 | ||||||
| chr2:190501029 | G | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 811 | chr2 | 190501029 | ||||||
| chr2:190501030 | A | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*812A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 812 | chr2 | 190501030 | ||||||
| chr2:190501031 | T | TTTTTGAA others(3): Show |
1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*813_*814insTTTTGA others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 814 | chr2 | 190501031 | ||||||
| chr2:190501033 | C | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 815 | chr2 | 190501033 | ||||||
| chr2:190501035 | G | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 817 | chr2 | 190501035 | ||||||
| chr2:190501040 | T | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 822 | chr2 | 190501040 | ||||||
| chr2:190501044 | C | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*826C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 826 | chr2 | 190501044 | ||||||
| chr2:190501048 | C | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*830C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 830 | chr2 | 190501048 | ||||||
| chr2:190501050 | C | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 832 | chr2 | 190501050 | ||||||
| chr2:190501054 | A | G | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*836A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 836 | chr2 | 190501054 | ||||||
| chr2:190501059 | C | G | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*841C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 841 | chr2 | 190501059 | ||||||
| chr2:190501062 | T | G | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*844T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 844 | chr2 | 190501062 | ||||||
| chr2:190501063 | C | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*845C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 845 | chr2 | 190501063 | ||||||
| chr2:190501065 | T | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*847T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 847 | chr2 | 190501065 | ||||||
| chr2:190501072 | A | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*854A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 854 | chr2 | 190501072 | ||||||
| chr2:190501085 | T | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*867T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 867 | chr2 | 190501085 | ||||||
| chr2:190501087 | A | T | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*869A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 869 | chr2 | 190501087 | ||||||
| chr2:190501088 | G | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*870G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 870 | chr2 | 190501088 | ||||||
| chr2:190501107 | C | A | 1 | a0001c0001t0017 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*889C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 889 | chr2 | 190501107 | ||||||
| chr2:190501127 | A | C | 1 | a0003c0003t0022 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 909 | chr2 | 190501127 | ||||||
| chr2:190501138 | A | G | 1 | a0001c0001t0021 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*920A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 920 | chr2 | 190501138 | ||||||
| chr2:190501255 | G | A | 2 | a0001c0001t0008 a0002c0002t0008 |
3 | HG03471.hp1 HG06807.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1037G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1037 | chr2 | 190501255 | ||||||
| chr2:190501292 | G | A | 1 | a0001c0001t0018 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1074G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1074 | chr2 | 190501292 | ||||||
| chr2:190501485 | G | A | 1 | a0002c0002t0009 | 3 | HG02074.hp2 NA18957.hp2 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1267G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1267 | chr2 | 190501485 | ||||||
| chr2:190501819 | G | A | 1 | a0002c0002t0019 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1601G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1601 | chr2 | 190501819 | ||||||
| chr2:190501853 | T | G | 8 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(5): Show |
57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1635T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1635 | chr2 | 190501853 | ||||||
| chr2:190501981 | A | G | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0016 others(3): Show |
88 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1763A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1763 | chr2 | 190501981 | ||||||
| chr2:190502110 | A | G | 2 | a0003c0003t0010 a0003c0003t0022 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1892A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1892 | chr2 | 190502110 | ||||||
| chr2:190502213 | G | A | 1 | a0001c0001t0020 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1995G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 1995 | chr2 | 190502213 | ||||||
| chr2:190502244 | G | A | 1 | a0001c0001t0012 | 2 | HG02145.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2026G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 2026 | chr2 | 190502244 | ||||||
| chr2:190502248 | CTT | C | 2 | a0003c0003t0010 a0003c0003t0022 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2034_*2035delTT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 8/8 | 2034 | INFO_REALIGN_3_PRIME | chr2 | 190502248 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190408511 | G | A | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG03453.hp2 HG03516.hp1 |
splice_region_variant&intron_variant | LOW | c.-176+8G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408511 | |||||||
| chr2:190408536 | C | T | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-176+33C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408536 | |||||||
| chr2:190408632 | C | T | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-176+129C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408632 | |||||||
| chr2:190408694 | G | GCTCC | 4 | a0002c0002t0001g0322 a0004c0004t0001g0321 a0004c0004t0001g0323 others(1): Show |
4 | HG02559.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176+209_-176+212d others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190408694 | ||||||
| chr2:190408694 | G | GCTCCCTC others(1): Show |
7 | a0001c0001t0002g0325 a0001c0001t0002g0326 a0001c0001t0002g0327 others(4): Show |
7 | HG02055.hp1 HG02622.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176+205_-176+212d others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190408694 | ||||||
| chr2:190408694 | GCTCCCTC others(1): Show |
G | 56 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(53): Show |
56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-176+205_-176+212d others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190408694 | ||||||
| chr2:190408754 | G | A | 85 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-176+251G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408754 | |||||||
| chr2:190408755 | G | C | 56 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(53): Show |
56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-176+252G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408755 | |||||||
| chr2:190408769 | T | A | 1 | a0001c0001t0003g0013 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-176+266T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190408769 | |||||||
| chr2:190409090 | G | C | 2 | a0002c0002t0001g0145 a0002c0002t0001g0146 |
2 | HG01255.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-176+587G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190409090 | |||||||
| chr2:190409267 | A | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-176+764A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190409267 | |||||||
| chr2:190409407 | A | G | 1 | a0002c0002t0001g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-176+904A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190409407 | |||||||
| chr2:190409483 | G | T | 1 | a0002c0002t0001g0318 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-176+980G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190409483 | |||||||
| chr2:190409543 | G | T | 1 | a0001c0001t0003g0068 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-176+1040G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190409543 | |||||||
| chr2:190410078 | C | T | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-176+1575C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410078 | |||||||
| chr2:190410368 | T | C | 1 | a0002c0002t0001g0147 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-176+1865T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410368 | |||||||
| chr2:190410525 | C | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG02135.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-176+2022C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410525 | |||||||
| chr2:190410537 | A | T | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-176+2034A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410537 | |||||||
| chr2:190410557 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-176+2054T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410557 | |||||||
| chr2:190410790 | G | A | 1 | a0002c0002t0005g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-176+2287G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410790 | |||||||
| chr2:190410801 | T | C | 4 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(1): Show |
4 | HG00741.hp2 HG01074.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-176+2298T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410801 | |||||||
| chr2:190410852 | T | TC | 68 | a0001c0001t0002g0313 a0001c0001t0003g0282 a0002c0002t0001g0010 others(65): Show |
69 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.-176+2350dupC | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190410852 | ||||||
| chr2:190410954 | G | T | 1 | a0001c0001t0002g0144 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-176+2451G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190410954 | |||||||
| chr2:190411009 | C | T | 68 | a0001c0001t0002g0313 a0001c0001t0003g0282 a0002c0002t0001g0010 others(65): Show |
69 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.-176+2506C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411009 | |||||||
| chr2:190411010 | G | A | 84 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0002g0001 others(81): Show |
89 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-176+2507G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411010 | |||||||
| chr2:190411011 | C | T | 34 | a0001c0001t0001g0148 a0001c0001t0001g0221 a0001c0001t0001g0222 others(31): Show |
35 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-176+2508C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411011 | |||||||
| chr2:190411074 | A | G | 1 | a0001c0001t0007g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-176+2571A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411074 | |||||||
| chr2:190411156 | CAGT | C | 9 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(6): Show |
9 | HG01433.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-176+2657_-176+265 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190411156 | ||||||
| chr2:190411158 | GTAGT | G | 75 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0002g0001 others(72): Show |
80 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-176+2657_-176+266 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190411158 | ||||||
| chr2:190411161 | G | GT | 30 | a0001c0001t0001g0242 a0001c0001t0001g0244 a0001c0001t0001g0245 others(27): Show |
30 | HG01169.hp2 HG01192.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.-176+2675dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190411161 | ||||||
| chr2:190411189 | C | G | 1 | a0002c0002t0001g0215 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-176+2686C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411189 | |||||||
| chr2:190411194 | T | C | 85 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-176+2691T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411194 | |||||||
| chr2:190411795 | C | T | 5 | a0001c0001t0001g0130 a0001c0001t0002g0129 a0001c0001t0002g0131 others(2): Show |
5 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176+3292C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411795 | |||||||
| chr2:190411885 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-176+3382C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411885 | |||||||
| chr2:190411944 | A | G | 2 | a0002c0002t0004g0213 a0002c0002t0004g0214 |
2 | HG01123.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-175-3348A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190411944 | |||||||
| chr2:190412495 | T | G | 1 | a0002c0002t0001g0150 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-175-2797T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190412495 | |||||||
| chr2:190412496 | A | T | 1 | a0002c0002t0001g0150 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-175-2796A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190412496 | |||||||
| chr2:190412565 | G | A | 1 | a0002c0002t0001g0252 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-175-2727G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190412565 | |||||||
| chr2:190412626 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-175-2666C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190412626 | |||||||
| chr2:190413184 | C | G | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-175-2108C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190413184 | |||||||
| chr2:190413615 | G | A | 234 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(231): Show |
245 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.-175-1677G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190413615 | |||||||
| chr2:190413671 | G | A | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-175-1621G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190413671 | |||||||
| chr2:190413692 | C | T | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-175-1600C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190413692 | |||||||
| chr2:190413912 | C | A | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-175-1380C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190413912 | |||||||
| chr2:190414005 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-175-1287G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190414005 | |||||||
| chr2:190414260 | A | G | 36 | a0001c0001t0001g0148 a0001c0001t0001g0221 a0001c0001t0001g0222 others(33): Show |
37 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.-175-1032A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190414260 | |||||||
| chr2:190414439 | G | A | 1 | a0002c0002t0001g0243 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-175-853G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190414439 | |||||||
| chr2:190414446 | T | TAAAAGAC others(30): Show |
1 | a0002c0002t0001g0243 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-175-836_-175-835i others(39): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 190414446 | ||||||
| chr2:190414640 | A | G | 2 | a0002c0002t0001g0310 a0002c0002t0001g0311 |
2 | NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-175-652A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 1/7 | chr2 | 190414640 | |||||||
| chr2:190415479 | A | G | 1 | a0001c0001t0003g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-54+66A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190415479 | |||||||
| chr2:190415709 | G | T | 329 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(326): Show |
341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.-54+296G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190415709 | |||||||
| chr2:190415943 | A | G | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-54+530A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190415943 | |||||||
| chr2:190416032 | A | C | 2 | a0002c0002t0001g0308 a0002c0002t0001g0309 |
2 | HG02040.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-54+619A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416032 | |||||||
| chr2:190416155 | A | G | 1 | a0002c0002t0001g0307 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-54+742A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416155 | |||||||
| chr2:190416306 | A | C | 32 | a0001c0001t0001g0148 a0001c0001t0001g0221 a0001c0001t0001g0222 others(29): Show |
33 | HG01192.hp1 HG01261.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.-54+893A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416306 | |||||||
| chr2:190416320 | C | G | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-54+907C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416320 | |||||||
| chr2:190416442 | A | C | 35 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0221 others(32): Show |
36 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.-54+1029A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416442 | |||||||
| chr2:190416594 | C | T | 56 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(53): Show |
56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-54+1181C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190416594 | |||||||
| chr2:190417182 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-54+1769A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417182 | |||||||
| chr2:190417268 | G | A | 329 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(326): Show |
341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.-54+1855G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417268 | |||||||
| chr2:190417465 | T | G | 2 | a0001c0001t0003g0016 a0001c0001t0003g0017 |
2 | HG01517.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-54+2052T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417465 | |||||||
| chr2:190417525 | A | G | 34 | a0001c0001t0001g0148 a0001c0001t0001g0221 a0001c0001t0001g0222 others(31): Show |
35 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-54+2112A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417525 | |||||||
| chr2:190417684 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-54+2271C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417684 | |||||||
| chr2:190417698 | T | C | 271 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(268): Show |
283 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.-54+2285T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417698 | |||||||
| chr2:190417703 | C | A | 151 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(148): Show |
157 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-54+2290C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190417703 | |||||||
| chr2:190417965 | G | GGT | 14 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0003g0016 others(11): Show |
15 | HG00140.hp2 HG01517.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.-54+2587_-54+2588d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | ||||||
| chr2:190417965 | G | GGTGT | 21 | a0001c0001t0001g0143 a0001c0001t0003g0059 a0001c0001t0021g0210 others(18): Show |
21 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.-54+2585_-54+2588d others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | ||||||
| chr2:190417965 | G | GGTGTGT | 57 | a0001c0001t0001g0148 a0001c0001t0001g0232 a0001c0001t0001g0233 others(54): Show |
60 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-54+2583_-54+2588d others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | ||||||
| chr2:190417965 | G | GGTGTGTG others(1): Show |
41 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(38): Show |
42 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-54+2581_-54+2588d others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | ||||||
| chr2:190417965 | G | GGTGTGTG others(3): Show |
12 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0002c0002t0001g0206 others(9): Show |
12 | HG01891.hp1 HG02486.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.-54+2579_-54+2588d others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | ||||||
| chr2:190417965 | G | GGTGTGTG others(5): Show |
5 | a0002c0002t0001g0303 a0002c0002t0001g0304 a0002c0002t0009g0305 others(2): Show |
5 | HG00639.hp2 HG01981.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+2577_-54+2588d others(14): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | ||||||
| chr2:190417965 | GGTGTGT | G | 4 | a0001c0001t0001g0221 a0001c0001t0001g0244 a0003c0003t0010g0330 others(1): Show |
4 | HG02717.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+2583_-54+2588d others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | ||||||
| chr2:190417965 | GGTGTGTG others(3): Show |
G | 75 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0003 others(72): Show |
80 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-54+2579_-54+2588d others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | ||||||
| chr2:190417965 | GGTGTGTG others(15): Show |
G | 1 | a0001c0001t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-54+2567_-54+2588d others(24): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417965 | ||||||
| chr2:190417998 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0012g0236 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+2588_-54+2589i others(14): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190417998 | ||||||
| chr2:190418000 | GTA | G | 4 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0058 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+2589_-54+2590d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190418000 | ||||||
| chr2:190418002 | A | G | 53 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-54+2589A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418002 | |||||||
| chr2:190418005 | T | A | 5 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(2): Show |
5 | HG02135.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+2592T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418005 | |||||||
| chr2:190418088 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-54+2675C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418088 | |||||||
| chr2:190418308 | T | C | 2 | a0001c0001t0003g0019 a0001c0001t0003g0061 |
2 | NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-54+2895T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418308 | |||||||
| chr2:190418523 | A | G | 2 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-54+3110A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418523 | |||||||
| chr2:190418752 | A | G | 329 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(326): Show |
341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.-54+3339A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418752 | |||||||
| chr2:190418774 | A | C | 1 | a0002c0002t0003g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-54+3361A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418774 | |||||||
| chr2:190418775 | A | G | 1 | a0002c0002t0001g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-54+3362A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418775 | |||||||
| chr2:190418982 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-54+3569C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190418982 | |||||||
| chr2:190419092 | A | G | 1 | a0001c0001t0003g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-54+3679A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419092 | |||||||
| chr2:190419181 | T | C | 1 | a0002c0002t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-54+3768T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419181 | |||||||
| chr2:190419244 | G | A | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-54+3831G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419244 | |||||||
| chr2:190419271 | C | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0251 |
2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-54+3858C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419271 | |||||||
| chr2:190419392 | C | T | 2 | a0002c0002t0001g0127 a0002c0002t0001g0128 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-54+3979C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419392 | |||||||
| chr2:190419625 | C | T | 1 | a0001c0001t0002g0126 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-54+4212C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419625 | |||||||
| chr2:190419840 | G | T | 1 | a0002c0002t0005g0200 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-54+4427G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419840 | |||||||
| chr2:190419929 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-54+4516A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190419929 | |||||||
| chr2:190420057 | CAA | C | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-54+4645_-54+4646d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420057 | |||||||
| chr2:190420139 | C | G | 44 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0073 others(41): Show |
48 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-54+4726C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420139 | |||||||
| chr2:190420172 | TATATAGC others(27): Show |
T | 329 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(326): Show |
341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.-54+4761_-54+4794d others(36): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190420172 | ||||||
| chr2:190420390 | T | G | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-54+4977T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420390 | |||||||
| chr2:190420391 | C | A | 1 | a0002c0002t0013g0314 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-54+4978C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420391 | |||||||
| chr2:190420531 | A | G | 1 | a0002c0002t0001g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-54+5118A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420531 | |||||||
| chr2:190420888 | T | C | 154 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(151): Show |
160 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.-54+5475T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190420888 | |||||||
| chr2:190421006 | A | G | 74 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0003 others(71): Show |
79 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-54+5593A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421006 | |||||||
| chr2:190421484 | A | G | 1 | a0001c0001t0003g0052 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-54+6071A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421484 | |||||||
| chr2:190421494 | G | GGTTT | 329 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(326): Show |
341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.-54+6084_-54+6085i others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190421494 | ||||||
| chr2:190421611 | C | A | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-54+6198C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421611 | |||||||
| chr2:190421658 | T | C | 329 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(326): Show |
341 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.-54+6245T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421658 | |||||||
| chr2:190421676 | A | C | 154 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(151): Show |
160 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.-54+6263A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421676 | |||||||
| chr2:190421725 | T | TAA | 114 | a0001c0001t0001g0097 a0001c0001t0001g0143 a0001c0001t0001g0148 others(111): Show |
120 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-54+6321_-54+6322d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190421725 | ||||||
| chr2:190421736 | T | A | 6 | a0001c0001t0001g0130 a0001c0001t0002g0129 a0001c0001t0002g0131 others(3): Show |
6 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54+6323T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421736 | |||||||
| chr2:190421758 | A | G | 270 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(267): Show |
282 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.-54+6345A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421758 | |||||||
| chr2:190421790 | A | C | 108 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(105): Show |
110 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.-54+6377A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421790 | |||||||
| chr2:190421932 | A | G | 271 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(268): Show |
283 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.-54+6519A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190421932 | |||||||
| chr2:190422065 | A | G | 56 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(53): Show |
56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-54+6652A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422065 | |||||||
| chr2:190422114 | C | T | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-54+6701C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422114 | |||||||
| chr2:190422396 | T | A | 154 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(151): Show |
160 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.-54+6983T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422396 | |||||||
| chr2:190422415 | T | A | 1 | a0001c0001t0002g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-54+7002T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422415 | |||||||
| chr2:190422651 | G | A | 1 | a0001c0001t0002g0325 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-54+7238G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422651 | |||||||
| chr2:190422656 | G | C | 117 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(114): Show |
123 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.-54+7243G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422656 | |||||||
| chr2:190422788 | T | C | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-54+7375T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422788 | |||||||
| chr2:190422861 | G | T | 1 | a0001c0001t0002g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-54+7448G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422861 | |||||||
| chr2:190422888 | C | CT | 8 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0126 others(5): Show |
10 | NA18949.hp1 NA18960.hp2 NA18980.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54+7484dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190422888 | ||||||
| chr2:190422957 | A | G | 80 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0002g0001 others(77): Show |
85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-54+7544A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422957 | |||||||
| chr2:190422959 | A | C | 80 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0002g0001 others(77): Show |
85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-54+7546A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190422959 | |||||||
| chr2:190423345 | G | T | 83 | a0001c0001t0003g0212 a0002c0002t0001g0002 a0002c0002t0001g0007 others(80): Show |
88 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-54+7932G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190423345 | |||||||
| chr2:190423688 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-54+8275G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190423688 | |||||||
| chr2:190423968 | T | C | 154 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(151): Show |
160 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.-54+8555T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190423968 | |||||||
| chr2:190424107 | A | G | 201 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(198): Show |
212 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.-54+8694A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190424107 | |||||||
| chr2:190424181 | C | T | 83 | a0001c0001t0003g0212 a0002c0002t0001g0002 a0002c0002t0001g0007 others(80): Show |
88 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-54+8768C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190424181 | |||||||
| chr2:190424235 | CT | C | 159 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0003 others(156): Show |
169 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.-54+8835delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190424235 | ||||||
| chr2:190424578 | G | A | 2 | a0001c0001t0001g0222 a0002c0002t0001g0206 |
2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-54+9165G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190424578 | |||||||
| chr2:190424706 | T | C | 3 | a0001c0001t0002g0003 a0001c0001t0002g0078 a0001c0001t0002g0125 |
4 | NA18986.hp2 NA18993.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+9293T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190424706 | |||||||
| chr2:190424785 | A | G | 70 | a0001c0001t0002g0313 a0001c0001t0003g0282 a0002c0002t0001g0010 others(67): Show |
71 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.-54+9372A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190424785 | |||||||
| chr2:190425290 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-54+9877C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425290 | |||||||
| chr2:190425408 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-54+9995C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425408 | |||||||
| chr2:190425473 | T | C | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-54+10060T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425473 | |||||||
| chr2:190425568 | T | G | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
10 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54+10155T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425568 | |||||||
| chr2:190425828 | T | C | 56 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(53): Show |
56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-53-10149T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425828 | |||||||
| chr2:190425886 | G | A | 1 | a0002c0002t0001g0276 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-53-10091G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190425886 | |||||||
| chr2:190426019 | A | T | 154 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(151): Show |
160 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.-53-9958A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190426019 | |||||||
| chr2:190426023 | T | C | 34 | a0001c0001t0001g0148 a0001c0001t0001g0221 a0001c0001t0001g0222 others(31): Show |
35 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-53-9954T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190426023 | |||||||
| chr2:190426555 | G | C | 1 | a0002c0002t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-53-9422G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190426555 | |||||||
| chr2:190426749 | G | A | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53-9228G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190426749 | |||||||
| chr2:190426828 | CTG | C | 34 | a0001c0001t0001g0148 a0001c0001t0001g0221 a0001c0001t0001g0222 others(31): Show |
35 | HG01168.hp1 HG01169.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-53-9146_-53-9145d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190426828 | ||||||
| chr2:190426914 | G | A | 1 | a0004c0004t0001g0321 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-53-9063G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190426914 | |||||||
| chr2:190427069 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-53-8908G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427069 | |||||||
| chr2:190427288 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-53-8689G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427288 | |||||||
| chr2:190427360 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-53-8617C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427360 | |||||||
| chr2:190427412 | C | T | 82 | a0001c0001t0003g0212 a0002c0002t0001g0002 a0002c0002t0001g0007 others(79): Show |
87 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-53-8565C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427412 | |||||||
| chr2:190427657 | T | C | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-8320T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427657 | |||||||
| chr2:190427727 | CT | C | 116 | a0001c0001t0001g0148 a0001c0001t0001g0221 a0001c0001t0001g0222 others(113): Show |
122 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-53-8239delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190427727 | ||||||
| chr2:190427846 | C | A | 44 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0073 others(41): Show |
48 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-53-8131C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427846 | |||||||
| chr2:190427963 | C | T | 1 | a0002c0002t0001g0170 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-53-8014C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427963 | |||||||
| chr2:190427981 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-53-7996C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427981 | |||||||
| chr2:190427983 | C | T | 1 | a0001c0001t0003g0013 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-53-7994C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190427983 | |||||||
| chr2:190428027 | C | G | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-53-7950C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428027 | |||||||
| chr2:190428071 | T | C | 82 | a0001c0001t0003g0212 a0002c0002t0001g0002 a0002c0002t0001g0007 others(79): Show |
87 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-53-7906T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428071 | |||||||
| chr2:190428083 | C | G | 82 | a0001c0001t0003g0212 a0002c0002t0001g0002 a0002c0002t0001g0007 others(79): Show |
87 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-53-7894C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428083 | |||||||
| chr2:190428085 | A | G | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-7892A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428085 | |||||||
| chr2:190428228 | C | T | 1 | a0001c0001t0007g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-53-7749C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428228 | |||||||
| chr2:190428240 | T | G | 5 | a0001c0001t0001g0130 a0001c0001t0002g0129 a0001c0001t0002g0131 others(2): Show |
5 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-53-7737T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428240 | |||||||
| chr2:190428329 | A | G | 82 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(79): Show |
87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-53-7648A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428329 | |||||||
| chr2:190428558 | T | A | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-53-7419T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428558 | |||||||
| chr2:190428572 | T | G | 2 | a0001c0001t0002g0122 a0002c0002t0001g0123 |
2 | NA18960.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-53-7405T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428572 | |||||||
| chr2:190428647 | ATGCT | A | 32 | a0001c0001t0001g0245 a0001c0001t0002g0001 a0001c0001t0002g0003 others(29): Show |
35 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.-53-7324_-53-7321d others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190428647 | ||||||
| chr2:190428650 | C | CTTAT | 26 | a0001c0001t0002g0018 a0001c0001t0002g0069 a0001c0001t0002g0070 others(23): Show |
26 | HG00323.hp1 HG00741.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-53-7325_-53-7324i others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190428650 | ||||||
| chr2:190428650 | CTTGCTTA others(1): Show |
C | 140 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0221 others(137): Show |
143 | HG00621.hp1 HG00741.hp1 HG01069.hp2 others(140): Show |
intron_variant | MODIFIER | c.-53-7324_-53-7317d others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190428650 | ||||||
| chr2:190428650 | CTTGCTTA others(5): Show |
C | 1 | a0002c0002t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-53-7324_-53-7313d others(14): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190428650 | ||||||
| chr2:190428653 | G | A | 153 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0002g0015 others(150): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-53-7324G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428653 | |||||||
| chr2:190428654 | C | T | 153 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0002g0015 others(150): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-53-7323C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428654 | |||||||
| chr2:190428874 | C | T | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-53-7103C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428874 | |||||||
| chr2:190428875 | A | G | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-7102A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428875 | |||||||
| chr2:190428969 | A | G | 328 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(325): Show |
340 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.-53-7008A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190428969 | |||||||
| chr2:190429046 | G | A | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-53-6931G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429046 | |||||||
| chr2:190429086 | A | G | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-6891A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429086 | |||||||
| chr2:190429127 | T | C | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-53-6850T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429127 | |||||||
| chr2:190429227 | C | CGT | 182 | a0001c0001t0001g0148 a0001c0001t0001g0221 a0001c0001t0001g0222 others(179): Show |
188 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(185): Show |
intron_variant | MODIFIER | c.-53-6729_-53-6728d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190429227 | ||||||
| chr2:190429364 | C | T | 5 | a0002c0002t0001g0002 a0002c0002t0001g0179 a0002c0002t0001g0197 others(2): Show |
7 | NA18941.hp2 NA18956.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53-6613C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429364 | |||||||
| chr2:190429388 | C | T | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-6589C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429388 | |||||||
| chr2:190429443 | A | T | 2 | a0002c0002t0001g0127 a0002c0002t0001g0128 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-53-6534A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429443 | |||||||
| chr2:190429448 | C | T | 1 | a0001c0001t0003g0052 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-53-6529C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429448 | |||||||
| chr2:190429454 | C | A | 44 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0073 others(41): Show |
48 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-53-6523C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429454 | |||||||
| chr2:190429534 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-53-6443G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429534 | |||||||
| chr2:190429583 | A | G | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-6394A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429583 | |||||||
| chr2:190429803 | A | C | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-6174A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429803 | |||||||
| chr2:190429999 | T | C | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-5978T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190429999 | |||||||
| chr2:190430009 | C | G | 2 | a0001c0001t0001g0251 a0002c0002t0001g0275 |
2 | HG02523.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-53-5968C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430009 | |||||||
| chr2:190430026 | G | C | 20 | a0001c0001t0002g0001 a0001c0001t0002g0076 a0001c0001t0002g0077 others(17): Show |
22 | HG00408.hp1 HG00423.hp1 HG02165.hp1 others(19): Show |
intron_variant | MODIFIER | c.-53-5951G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430026 | |||||||
| chr2:190430207 | C | CT | 143 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(140): Show |
149 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.-53-5754dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430207 | ||||||
| chr2:190430207 | CT | C | 7 | a0001c0001t0001g0237 a0001c0001t0002g0094 a0001c0001t0003g0027 others(4): Show |
7 | HG00323.hp2 HG01074.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53-5754delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430207 | ||||||
| chr2:190430278 | T | C | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-5699T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430278 | |||||||
| chr2:190430320 | A | G | 1 | a0002c0002t0001g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-53-5657A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430320 | |||||||
| chr2:190430350 | C | T | 56 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(53): Show |
56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-53-5627C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430350 | |||||||
| chr2:190430359 | G | A | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-5618G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430359 | |||||||
| chr2:190430389 | T | G | 1 | a0001c0001t0003g0053 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-53-5588T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430389 | |||||||
| chr2:190430621 | A | G | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-53-5356A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430621 | |||||||
| chr2:190430631 | C | T | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-5346C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430631 | |||||||
| chr2:190430698 | C | A | 1 | a0002c0002t0001g0280 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-53-5279C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430698 | |||||||
| chr2:190430718 | GGGTACAC others(5): Show |
G | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-5258_-53-5247d others(14): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430718 | |||||||
| chr2:190430738 | G | A | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-5239G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430738 | |||||||
| chr2:190430769 | C | A | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-53-5208C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430769 | |||||||
| chr2:190430799 | C | CCCCCCCC others(88): Show |
1 | a0002c0002t0001g0153 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-53-5160_-53-5159i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430799 | ||||||
| chr2:190430799 | C | CCCCCCCC others(88): Show |
51 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(48): Show |
52 | HG00609.hp2 HG00621.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.-53-5160_-53-5159i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430799 | ||||||
| chr2:190430799 | C | CCCCCCCC others(88): Show |
1 | a0002c0002t0001g0252 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-53-5160_-53-5159i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430799 | ||||||
| chr2:190430799 | C | CCCCCCCC others(89): Show |
2 | a0002c0002t0001g0276 a0002c0002t0001g0316 |
2 | HG02056.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-53-5171_-53-5170i others(98): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430799 | ||||||
| chr2:190430800 | CCCCCCCA others(40): Show |
C | 6 | a0001c0001t0001g0130 a0001c0001t0002g0129 a0001c0001t0002g0131 others(3): Show |
6 | HG01106.hp1 HG02083.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-53-5147_-53-5101d others(49): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430800 | ||||||
| chr2:190430818 | G | C | 97 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(94): Show |
102 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-53-5159G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430818 | |||||||
| chr2:190430820 | A | G | 55 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(52): Show |
56 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-53-5157A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430820 | |||||||
| chr2:190430834 | C | T | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-53-5143C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430834 | |||||||
| chr2:190430855 | C | T | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-5122C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430855 | |||||||
| chr2:190430864 | C | CGGACGGG others(88): Show |
1 | a0002c0002t0001g0307 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | ||||||
| chr2:190430864 | C | CGGACGGG others(88): Show |
88 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(85): Show |
93 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-53-5101_-53-5100i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | ||||||
| chr2:190430864 | C | CGGACGGG others(89): Show |
1 | a0002c0002t0001g0274 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(98): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | ||||||
| chr2:190430864 | C | CGGACGGG others(71): Show |
1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(80): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | ||||||
| chr2:190430864 | C | CGGACGGG others(89): Show |
1 | a0002c0002t0001g0217 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(98): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | ||||||
| chr2:190430864 | C | CGGGCGGG others(40): Show |
3 | a0002c0002t0005g0149 a0002c0002t0005g0218 a0002c0002t0008g0211 |
3 | HG02280.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-53-5111_-53-5110i others(49): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430864 | ||||||
| chr2:190430864 | C | T | 58 | a0001c0001t0002g0313 a0001c0001t0003g0029 a0001c0001t0003g0049 others(55): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.-53-5113C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430864 | |||||||
| chr2:190430867 | A | ACGGGGCG others(41): Show |
1 | a0002c0002t0001g0176 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(50): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430867 | ||||||
| chr2:190430873 | C | CGGCCGGC others(88): Show |
1 | a0002c0002t0001g0275 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-53-5101_-53-5100i others(97): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190430873 | ||||||
| chr2:190430948 | C | T | 1 | a0002c0002t0001g0285 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-53-5029C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190430948 | |||||||
| chr2:190431006 | ACGCTCCT others(33): Show |
A | 46 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0073 others(43): Show |
50 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-53-4943_-53-4904d others(42): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190431006 | ||||||
| chr2:190431026 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-53-4951G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431026 | |||||||
| chr2:190431048 | G | A | 1 | a0002c0002t0001g0281 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-53-4929G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431048 | |||||||
| chr2:190431087 | C | T | 58 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0069 others(55): Show |
63 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-53-4890C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431087 | |||||||
| chr2:190431114 | G | A | 2 | a0002c0002t0001g0181 a0002c0002t0001g0185 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-53-4863G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431114 | |||||||
| chr2:190431143 | G | A | 3 | a0001c0001t0002g0325 a0001c0001t0002g0326 a0001c0001t0002g0327 |
3 | HG02622.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-53-4834G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431143 | |||||||
| chr2:190431194 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-53-4783G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431194 | |||||||
| chr2:190431244 | C | T | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53-4733C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431244 | |||||||
| chr2:190431297 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0245 |
2 | HG01261.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-53-4680C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431297 | |||||||
| chr2:190431382 | G | A | 2 | a0001c0001t0012g0236 a0001c0001t0012g0247 |
2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-53-4595G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431382 | |||||||
| chr2:190431453 | G | A | 2 | a0001c0001t0002g0122 a0002c0002t0001g0123 |
2 | NA18960.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-53-4524G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431453 | |||||||
| chr2:190431490 | A | G | 152 | a0001c0001t0002g0313 a0001c0001t0003g0212 a0001c0001t0003g0282 others(149): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.-53-4487A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431490 | |||||||
| chr2:190431506 | T | C | 296 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(293): Show |
307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-53-4471T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431506 | |||||||
| chr2:190431524 | G | C | 1 | a0002c0002t0001g0197 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-53-4453G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431524 | |||||||
| chr2:190431547 | A | G | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-53-4430A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431547 | |||||||
| chr2:190431570 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-53-4407C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431570 | |||||||
| chr2:190431690 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-53-4287G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431690 | |||||||
| chr2:190431695 | AAG | A | 58 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(55): Show |
58 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-53-4277_-53-4276d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190431695 | ||||||
| chr2:190431703 | G | A | 80 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0002g0001 others(77): Show |
85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-53-4274G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431703 | |||||||
| chr2:190431892 | T | A | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-53-4085T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190431892 | |||||||
| chr2:190431997 | TCTGATTT others(7): Show |
T | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-3974_-53-3961d others(16): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190431997 | ||||||
| chr2:190432245 | G | A | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-53-3732G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432245 | |||||||
| chr2:190432320 | C | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0244 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-53-3657C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432320 | |||||||
| chr2:190432394 | C | A | 1 | a0002c0002t0001g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-53-3583C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432394 | |||||||
| chr2:190432425 | T | G | 1 | a0002c0002t0001g0304 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-53-3552T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432425 | |||||||
| chr2:190432426 | G | T | 1 | a0002c0002t0001g0304 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-53-3551G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432426 | |||||||
| chr2:190432427 | T | G | 1 | a0002c0002t0001g0304 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-53-3550T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432427 | |||||||
| chr2:190432721 | T | C | 294 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(291): Show |
305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.-53-3256T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432721 | |||||||
| chr2:190432821 | C | T | 1 | a0002c0002t0001g0268 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-53-3156C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432821 | |||||||
| chr2:190432840 | A | T | 1 | a0006c0008t0003g0028 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-53-3137A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432840 | |||||||
| chr2:190432842 | T | A | 136 | a0001c0001t0003g0212 a0001c0001t0003g0282 a0002c0002t0001g0002 others(133): Show |
141 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.-53-3135T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432842 | |||||||
| chr2:190432869 | T | C | 1 | a0001c0001t0003g0016 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-53-3108T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190432869 | |||||||
| chr2:190433047 | C | T | 151 | a0001c0001t0003g0212 a0002c0002t0001g0002 a0002c0002t0001g0007 others(148): Show |
157 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-53-2930C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190433047 | |||||||
| chr2:190433183 | A | C | 1 | a0002c0002t0013g0314 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-53-2794A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190433183 | |||||||
| chr2:190433260 | AT | A | 4 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0030 others(1): Show |
4 | HG01069.hp1 HG01243.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-2713delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190433260 | ||||||
| chr2:190433812 | C | G | 1 | a0001c0001t0002g0093 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-53-2165C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190433812 | |||||||
| chr2:190433886 | C | T | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | NA18959.hp2 NA18997.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-53-2091C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190433886 | |||||||
| chr2:190434017 | C | A | 1 | a0001c0001t0003g0052 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-53-1960C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434017 | |||||||
| chr2:190434098 | G | C | 150 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(147): Show |
156 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.-53-1879G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434098 | |||||||
| chr2:190434182 | C | CA | 216 | a0001c0001t0001g0222 a0001c0001t0002g0014 a0001c0001t0002g0015 others(213): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.-53-1782dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190434182 | ||||||
| chr2:190434196 | G | A | 1 | a0002c0002t0001g0304 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-53-1781G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434196 | |||||||
| chr2:190434240 | G | A | 1 | a0002c0002t0001g0286 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-53-1737G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434240 | |||||||
| chr2:190434326 | A | G | 2 | a0003c0003t0022g0207 a0008c0009t0015g0208 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-53-1651A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434326 | |||||||
| chr2:190434576 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-53-1401C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434576 | |||||||
| chr2:190434580 | C | T | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-53-1397C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434580 | |||||||
| chr2:190434795 | G | A | 16 | a0002c0002t0001g0252 a0002c0002t0001g0253 a0002c0002t0001g0255 others(13): Show |
16 | HG01981.hp1 HG02015.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-53-1182G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434795 | |||||||
| chr2:190434983 | G | A | 1 | a0001c0001t0003g0031 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-53-994G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190434983 | |||||||
| chr2:190435171 | G | A | 296 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(293): Show |
307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-53-806G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435171 | |||||||
| chr2:190435270 | G | T | 296 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(293): Show |
307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-53-707G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435270 | |||||||
| chr2:190435392 | G | A | 215 | a0001c0001t0001g0143 a0001c0001t0002g0014 a0001c0001t0002g0015 others(212): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.-53-585G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435392 | |||||||
| chr2:190435452 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-53-525C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435452 | |||||||
| chr2:190435637 | AAC | A | 150 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(147): Show |
156 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.-53-338_-53-337del others(2): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 190435637 | ||||||
| chr2:190435676 | A | G | 151 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(148): Show |
157 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-53-301A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435676 | |||||||
| chr2:190435713 | A | G | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-53-264A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435713 | |||||||
| chr2:190435796 | G | A | 2 | a0002c0002t0001g0196 a0002c0002t0001g0319 |
2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-53-181G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 2/7 | chr2 | 190435796 | |||||||
| chr2:190437577 | C | T | 1 | a0002c0002t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1532+16C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190437577 | |||||||
| chr2:190438013 | C | T | 103 | a0001c0001t0001g0130 a0002c0002t0001g0008 a0002c0002t0001g0009 others(100): Show |
106 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1532+452C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438013 | |||||||
| chr2:190438025 | T | C | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+464T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438025 | |||||||
| chr2:190438061 | G | A | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1532+500G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438061 | |||||||
| chr2:190438176 | T | C | 1 | a0002c0002t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1532+615T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438176 | |||||||
| chr2:190438181 | C | G | 2 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1532+620C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438181 | |||||||
| chr2:190438215 | T | TA | 301 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0222 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.1532+665dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190438215 | ||||||
| chr2:190438215 | T | TAA | 8 | a0002c0002t0001g0123 a0002c0002t0001g0145 a0002c0002t0001g0146 others(5): Show |
8 | HG01255.hp2 HG03195.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1532+664_1532+665d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190438215 | ||||||
| chr2:190438305 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1532+744C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438305 | |||||||
| chr2:190438313 | C | T | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+752C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438313 | |||||||
| chr2:190438393 | G | A | 1 | a0001c0001t0002g0018 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1532+832G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438393 | |||||||
| chr2:190438520 | A | C | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+959A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438520 | |||||||
| chr2:190438531 | C | T | 1 | a0001c0001t0003g0052 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1532+970C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438531 | |||||||
| chr2:190438673 | G | A | 1 | a0002c0002t0001g0254 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1532+1112G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438673 | |||||||
| chr2:190438794 | T | G | 2 | a0001c0001t0003g0022 a0001c0001t0003g0023 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1532+1233T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438794 | |||||||
| chr2:190438799 | A | G | 61 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(58): Show |
61 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1532+1238A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438799 | |||||||
| chr2:190438986 | G | T | 2 | a0002c0002t0001g0173 a0002c0002t0013g0302 |
2 | HG00639.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.1532+1425G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438986 | |||||||
| chr2:190438987 | G | A | 2 | a0002c0002t0001g0173 a0002c0002t0013g0302 |
2 | HG00639.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.1532+1426G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190438987 | |||||||
| chr2:190439260 | C | T | 103 | a0001c0001t0001g0130 a0002c0002t0001g0008 a0002c0002t0001g0009 others(100): Show |
106 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1532+1699C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439260 | |||||||
| chr2:190439423 | A | G | 219 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0002g0014 others(216): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1532+1862A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439423 | |||||||
| chr2:190439533 | T | C | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+1972T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439533 | |||||||
| chr2:190439643 | T | G | 1 | a0002c0002t0001g0262 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1532+2082T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439643 | |||||||
| chr2:190439786 | T | C | 1 | a0005c0005t0001g0284 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1532+2225T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439786 | |||||||
| chr2:190439887 | T | A | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+2326T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190439887 | |||||||
| chr2:190440034 | T | C | 1 | a0002c0002t0001g0316 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1532+2473T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440034 | |||||||
| chr2:190440286 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1532+2725C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440286 | |||||||
| chr2:190440309 | A | G | 2 | a0002c0002t0008g0211 a0002c0011t0001g0320 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1532+2748A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440309 | |||||||
| chr2:190440760 | C | T | 2 | a0001c0001t0001g0230 a0002c0002t0001g0219 |
2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1532+3199C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440760 | |||||||
| chr2:190440808 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1532+3247T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440808 | |||||||
| chr2:190440821 | A | G | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1532+3260A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440821 | |||||||
| chr2:190440921 | C | T | 153 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0002c0002t0001g0002 others(150): Show |
160 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.1532+3360C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440921 | |||||||
| chr2:190440936 | G | A | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+3375G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190440936 | |||||||
| chr2:190441094 | C | G | 1 | a0001c0001t0002g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1532+3533C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441094 | |||||||
| chr2:190441098 | T | C | 215 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0002g0014 others(212): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1532+3537T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441098 | |||||||
| chr2:190441180 | T | A | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1532+3619T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441180 | |||||||
| chr2:190441257 | T | C | 218 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0002g0014 others(215): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1532+3696T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441257 | |||||||
| chr2:190441307 | G | A | 1 | a0002c0002t0001g0263 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1532+3746G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441307 | |||||||
| chr2:190441422 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1532+3861G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441422 | |||||||
| chr2:190441428 | C | A | 1 | a0001c0001t0002g0102 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1532+3867C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441428 | |||||||
| chr2:190441488 | G | A | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1532+3927G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441488 | |||||||
| chr2:190441813 | C | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1532+4252C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441813 | |||||||
| chr2:190441816 | C | T | 165 | a0001c0001t0001g0130 a0001c0001t0002g0014 a0001c0001t0002g0015 others(162): Show |
168 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1532+4255C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190441816 | |||||||
| chr2:190442000 | A | G | 219 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0002g0014 others(216): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1532+4439A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442000 | |||||||
| chr2:190442164 | C | G | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+4603C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442164 | |||||||
| chr2:190442374 | T | G | 2 | a0001c0001t0012g0236 a0001c0001t0012g0247 |
2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1532+4813T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442374 | |||||||
| chr2:190442493 | C | G | 215 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0002g0014 others(212): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1532+4932C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442493 | |||||||
| chr2:190442541 | T | C | 2 | a0002c0002t0001g0201 a0002c0002t0001g0322 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1532+4980T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442541 | |||||||
| chr2:190442614 | G | A | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+5053G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442614 | |||||||
| chr2:190442682 | G | T | 103 | a0001c0001t0001g0130 a0002c0002t0001g0008 a0002c0002t0001g0009 others(100): Show |
106 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1532+5121G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442682 | |||||||
| chr2:190442818 | T | A | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+5257T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442818 | |||||||
| chr2:190442821 | T | C | 2 | a0002c0002t0001g0181 a0002c0002t0001g0185 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1532+5260T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442821 | |||||||
| chr2:190442836 | C | T | 166 | a0001c0001t0001g0130 a0001c0001t0001g0222 a0001c0001t0002g0014 others(163): Show |
169 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1532+5275C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442836 | |||||||
| chr2:190442900 | G | A | 2 | a0001c0001t0003g0022 a0001c0001t0003g0023 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1532+5339G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190442900 | |||||||
| chr2:190443751 | G | T | 4 | a0001c0001t0002g0129 a0001c0001t0002g0131 a0001c0001t0002g0132 others(1): Show |
4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1532+6190G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190443751 | |||||||
| chr2:190443847 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1532+6286G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190443847 | |||||||
| chr2:190443906 | G | A | 1 | a0002c0002t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1532+6345G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190443906 | |||||||
| chr2:190444066 | G | T | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+6505G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444066 | |||||||
| chr2:190444124 | T | C | 1 | a0001c0001t0002g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1532+6563T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444124 | |||||||
| chr2:190444145 | T | C | 1 | a0002c0002t0009g0305 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1532+6584T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444145 | |||||||
| chr2:190444338 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1532+6777C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444338 | |||||||
| chr2:190444563 | T | C | 7 | a0001c0001t0002g0095 a0001c0001t0002g0120 a0001c0001t0002g0223 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1532+7002T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444563 | |||||||
| chr2:190444572 | C | T | 2 | a0002c0002t0008g0202 a0002c0002t0008g0211 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1532+7011C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444572 | |||||||
| chr2:190444663 | C | T | 3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0137 |
3 | HG02145.hp1 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1532+7102C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444663 | |||||||
| chr2:190444880 | A | G | 1 | a0002c0002t0001g0169 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1532+7319A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444880 | |||||||
| chr2:190444958 | A | G | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1532+7397A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444958 | |||||||
| chr2:190444997 | C | T | 2 | a0002c0002t0001g0220 a0002c0002t0001g0243 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1532+7436C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190444997 | |||||||
| chr2:190445129 | G | C | 1 | a0002c0002t0005g0187 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1532+7568G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445129 | |||||||
| chr2:190445281 | T | G | 2 | a0002c0002t0001g0269 a0002c0002t0001g0286 |
2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1532+7720T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445281 | |||||||
| chr2:190445343 | C | T | 2 | a0002c0002t0008g0202 a0002c0002t0008g0211 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1532+7782C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445343 | |||||||
| chr2:190445392 | A | G | 61 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(58): Show |
61 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1532+7831A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445392 | |||||||
| chr2:190445457 | C | CA | 79 | a0001c0001t0001g0097 a0001c0001t0001g0246 a0001c0001t0002g0001 others(76): Show |
84 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1532+7907dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445457 | ||||||
| chr2:190445457 | C | CAA | 63 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(60): Show |
63 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1532+7906_1532+790 others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445457 | ||||||
| chr2:190445457 | C | CAAAA | 32 | a0001c0001t0001g0130 a0002c0002t0001g0008 a0002c0002t0001g0009 others(29): Show |
34 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1532+7904_1532+790 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445457 | ||||||
| chr2:190445457 | C | CAAAAA | 60 | a0002c0002t0001g0010 a0002c0002t0001g0123 a0002c0002t0001g0127 others(57): Show |
61 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1532+7903_1532+790 others(9): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445457 | ||||||
| chr2:190445469 | C | A | 4 | a0001c0001t0002g0104 a0001c0001t0002g0105 a0001c0001t0002g0121 others(1): Show |
4 | HG00544.hp2 NA18747.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1532+7908C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445469 | |||||||
| chr2:190445473 | G | A | 164 | a0001c0001t0001g0130 a0001c0001t0002g0014 a0001c0001t0002g0015 others(161): Show |
167 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1532+7912G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445473 | |||||||
| chr2:190445497 | G | A | 1 | a0001c0001t0018g0054 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1532+7936G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445497 | |||||||
| chr2:190445499 | A | AT | 164 | a0001c0001t0001g0130 a0001c0001t0002g0014 a0001c0001t0002g0015 others(161): Show |
167 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1532+7948dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445499 | ||||||
| chr2:190445510 | C | T | 2 | a0001c0001t0002g0080 a0001c0001t0002g0090 |
2 | NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1532+7949C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445510 | |||||||
| chr2:190445704 | G | A | 61 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(58): Show |
61 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1532+8143G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445704 | |||||||
| chr2:190445743 | T | C | 3 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 |
3 | NA18959.hp2 NA18997.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1532+8182T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445743 | |||||||
| chr2:190445802 | CGTG | C | 99 | a0001c0001t0001g0130 a0002c0002t0001g0008 a0002c0002t0001g0009 others(96): Show |
102 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.1532+8244_1532+824 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445802 | ||||||
| chr2:190445858 | G | A | 9 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0101 others(6): Show |
9 | HG01891.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1532+8297G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190445858 | |||||||
| chr2:190445861 | A | AT | 14 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(11): Show |
14 | HG00323.hp1 HG00741.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1532+8308dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190445861 | ||||||
| chr2:190446270 | A | C | 1 | a0002c0002t0001g0215 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1532+8709A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446270 | |||||||
| chr2:190446286 | A | G | 218 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0002g0014 others(215): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1532+8725A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446286 | |||||||
| chr2:190446332 | C | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0118 |
2 | HG01243.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1532+8771C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446332 | |||||||
| chr2:190446333 | A | T | 1 | a0001c0001t0003g0050 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1532+8772A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446333 | |||||||
| chr2:190446594 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1532+9033G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446594 | |||||||
| chr2:190446684 | T | C | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1532+9123T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446684 | |||||||
| chr2:190446770 | A | T | 2 | a0001c0001t0003g0063 a0001c0001t0017g0044 |
2 | NA18963.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1532+9209A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446770 | |||||||
| chr2:190446857 | C | T | 1 | a0001c0001t0018g0054 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1532+9296C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190446857 | |||||||
| chr2:190447098 | A | AT | 62 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+9537_1532+953 others(5): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447098 | |||||||
| chr2:190447142 | C | T | 2 | a0002c0002t0001g0258 a0002c0002t0019g0295 |
2 | NA18940.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1532+9581C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447142 | |||||||
| chr2:190447158 | G | A | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+9597G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447158 | |||||||
| chr2:190447160 | C | G | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+9599C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447160 | |||||||
| chr2:190447161 | A | G | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+9600A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447161 | |||||||
| chr2:190447377 | T | C | 1 | a0002c0002t0001g0184 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1532+9816T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447377 | |||||||
| chr2:190447413 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1532+9852G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447413 | |||||||
| chr2:190447498 | GTCATAGC others(5): Show |
G | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+9939_1532+995 others(16): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190447498 | ||||||
| chr2:190447761 | G | C | 19 | a0001c0001t0001g0130 a0002c0002t0001g0008 a0002c0002t0001g0009 others(16): Show |
21 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1532+10200G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447761 | |||||||
| chr2:190447779 | G | T | 1 | a0001c0001t0003g0021 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1532+10218G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447779 | |||||||
| chr2:190447937 | A | C | 1 | a0001c0001t0002g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1532+10376A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190447937 | |||||||
| chr2:190448145 | C | A | 298 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(295): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1532+10584C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448145 | |||||||
| chr2:190448180 | T | C | 62 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+10619T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448180 | |||||||
| chr2:190448423 | T | C | 3 | a0002c0002t0004g0006 a0002c0002t0004g0154 a0002c0002t0004g0163 |
4 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1532+10862T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448423 | |||||||
| chr2:190448603 | G | A | 99 | a0001c0001t0001g0130 a0002c0002t0001g0008 a0002c0002t0001g0009 others(96): Show |
102 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.1532+11042G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448603 | |||||||
| chr2:190448669 | G | C | 4 | a0002c0002t0001g0002 a0002c0002t0001g0197 a0002c0002t0001g0198 others(1): Show |
6 | NA18941.hp2 NA18956.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.1532+11108G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448669 | |||||||
| chr2:190448918 | C | T | 2 | a0002c0002t0004g0154 a0002c0002t0004g0163 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1532+11357C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448918 | |||||||
| chr2:190448986 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1532+11425A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190448986 | |||||||
| chr2:190449172 | A | G | 62 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+11611A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449172 | |||||||
| chr2:190449176 | T | G | 59 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(56): Show |
59 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1532+11615T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449176 | |||||||
| chr2:190449178 | T | C | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+11617T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449178 | |||||||
| chr2:190449662 | A | AC | 68 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(65): Show |
68 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1532+12101_1532+12 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449662 | |||||||
| chr2:190449842 | C | T | 2 | a0002c0002t0001g0220 a0002c0002t0001g0243 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1532+12281C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449842 | |||||||
| chr2:190449878 | G | C | 61 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(58): Show |
61 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1532+12317G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449878 | |||||||
| chr2:190449878 | G | T | 1 | a0001c0001t0003g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1532+12317G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449878 | |||||||
| chr2:190449900 | A | G | 1 | a0002c0002t0001g0294 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1532+12339A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449900 | |||||||
| chr2:190449930 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1532+12369G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449930 | |||||||
| chr2:190449976 | G | A | 2 | a0002c0002t0001g0188 a0002c0002t0001g0204 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1532+12415G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190449976 | |||||||
| chr2:190450032 | A | T | 2 | a0001c0001t0003g0019 a0001c0001t0003g0061 |
2 | NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1532+12471A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450032 | |||||||
| chr2:190450153 | T | C | 3 | a0002c0002t0008g0202 a0002c0002t0008g0211 a0002c0011t0001g0320 |
3 | HG01884.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1532+12592T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450153 | |||||||
| chr2:190450291 | G | A | 1 | a0002c0002t0001g0260 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1532+12730G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450291 | |||||||
| chr2:190450312 | C | T | 1 | a0002c0002t0001g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1532+12751C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450312 | |||||||
| chr2:190450419 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1532+12858T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450419 | |||||||
| chr2:190450488 | C | CT | 68 | a0001c0001t0001g0143 a0001c0001t0001g0222 a0001c0001t0001g0224 others(65): Show |
72 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1532+12948dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450488 | ||||||
| chr2:190450488 | C | CTT | 160 | a0001c0001t0001g0130 a0001c0001t0002g0001 a0001c0001t0002g0003 others(157): Show |
168 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1532+12947_1532+12 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450488 | ||||||
| chr2:190450488 | C | CTTT | 17 | a0001c0001t0002g0072 a0001c0001t0002g0077 a0001c0001t0002g0088 others(14): Show |
17 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1532+12946_1532+12 others(9): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450488 | ||||||
| chr2:190450488 | C | CTTTT | 50 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0313 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1532+12945_1532+12 others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450488 | ||||||
| chr2:190450488 | C | CTTTTT | 9 | a0001c0001t0002g0018 a0001c0001t0003g0021 a0001c0001t0003g0025 others(6): Show |
9 | HG01243.hp2 HG02602.hp1 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.1532+12944_1532+12 others(11): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450488 | ||||||
| chr2:190450519 | G | T | 62 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+12958G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450519 | |||||||
| chr2:190450589 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1532+13028C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450589 | |||||||
| chr2:190450631 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1532+13070T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450631 | |||||||
| chr2:190450752 | G | A | 1 | a0002c0002t0003g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1532+13191G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450752 | |||||||
| chr2:190450803 | TTC | T | 6 | a0002c0002t0001g0008 a0002c0002t0001g0182 a0002c0002t0001g0183 others(3): Show |
7 | HG00423.hp2 HG00609.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1532+13244_1532+13 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190450803 | ||||||
| chr2:190450922 | T | C | 15 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0174 others(12): Show |
17 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1532+13361T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190450922 | |||||||
| chr2:190451069 | C | G | 1 | a0002c0002t0001g0304 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1532+13508C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451069 | |||||||
| chr2:190451072 | T | C | 1 | a0002c0002t0001g0304 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1532+13511T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451072 | |||||||
| chr2:190451073 | G | T | 1 | a0002c0002t0001g0304 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1532+13512G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451073 | |||||||
| chr2:190451149 | G | T | 62 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+13588G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451149 | |||||||
| chr2:190451307 | G | C | 1 | a0001c0001t0003g0282 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1532+13746G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451307 | |||||||
| chr2:190451322 | T | C | 62 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1532+13761T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190451322 | |||||||
| chr2:190452269 | T | C | 298 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(295): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1532+14708T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190452269 | |||||||
| chr2:190452639 | C | G | 1 | a0002c0002t0009g0296 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1532+15078C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190452639 | |||||||
| chr2:190452784 | T | C | 298 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(295): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1532+15223T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190452784 | |||||||
| chr2:190452950 | C | T | 218 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0002g0014 others(215): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1532+15389C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190452950 | |||||||
| chr2:190453069 | G | A | 3 | a0001c0001t0003g0034 a0001c0001t0003g0056 a0001c0001t0003g0057 |
3 | HG00735.hp2 HG01070.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1532+15508G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453069 | |||||||
| chr2:190453222 | C | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1532+15661C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453222 | |||||||
| chr2:190453270 | C | A | 2 | a0002c0002t0001g0127 a0002c0002t0001g0128 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1532+15709C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453270 | |||||||
| chr2:190453294 | G | C | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1532+15733G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453294 | |||||||
| chr2:190453332 | A | G | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1532+15771A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453332 | |||||||
| chr2:190453368 | T | C | 1 | a0007c0006t0001g0324 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1532+15807T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453368 | |||||||
| chr2:190453427 | T | C | 26 | a0001c0001t0001g0130 a0002c0002t0001g0008 a0002c0002t0001g0009 others(23): Show |
28 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+15866T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453427 | |||||||
| chr2:190453454 | C | G | 1 | a0001c0001t0003g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1532+15893C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453454 | |||||||
| chr2:190453530 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1532+15969C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453530 | |||||||
| chr2:190453756 | C | G | 3 | a0002c0002t0008g0202 a0002c0002t0008g0211 a0002c0011t0001g0320 |
3 | HG01884.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-16002C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190453756 | |||||||
| chr2:190454050 | T | C | 160 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0002g0122 others(157): Show |
169 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.1533-15708T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454050 | |||||||
| chr2:190454084 | G | A | 2 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1533-15674G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454084 | |||||||
| chr2:190454268 | C | G | 9 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0087 others(6): Show |
9 | NA18940.hp2 NA18956.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.1533-15490C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454268 | |||||||
| chr2:190454335 | T | C | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-15423T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454335 | |||||||
| chr2:190454358 | C | T | 1 | a0002c0002t0001g0162 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1533-15400C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454358 | |||||||
| chr2:190454383 | C | A | 1 | a0002c0002t0001g0307 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1533-15375C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454383 | |||||||
| chr2:190454513 | G | A | 2 | a0002c0002t0001g0073 a0002c0002t0001g0074 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1533-15245G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454513 | |||||||
| chr2:190454520 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1533-15238T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454520 | |||||||
| chr2:190454534 | CCCTTCCC others(15): Show |
C | 1 | a0002c0002t0001g0260 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1533-15221_1533-15 others(28): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454534 | ||||||
| chr2:190454687 | A | G | 1 | a0001c0001t0007g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1533-15071A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454687 | |||||||
| chr2:190454932 | G | GTATGTA | 44 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0229 others(41): Show |
45 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1533-14763_1533-14 others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | ||||||
| chr2:190454932 | G | GTATGTAT others(5): Show |
30 | a0001c0001t0001g0239 a0001c0001t0007g0011 a0002c0002t0001g0123 others(27): Show |
30 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1533-14769_1533-14 others(18): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | ||||||
| chr2:190454932 | G | GTATGTAT others(11): Show |
13 | a0001c0001t0001g0224 a0001c0001t0001g0230 a0001c0001t0001g0234 others(10): Show |
13 | HG01255.hp2 HG01261.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1533-14775_1533-14 others(24): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | ||||||
| chr2:190454932 | G | GTATGTAT others(17): Show |
3 | a0001c0001t0001g0225 a0001c0001t0001g0233 a0001c0001t0001g0241 |
3 | HG01496.hp1 HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1533-14781_1533-14 others(30): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | ||||||
| chr2:190454932 | G | GTATGTAT others(23): Show |
7 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0242 others(4): Show |
7 | HG01884.hp1 HG01981.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533-14787_1533-14 others(36): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | ||||||
| chr2:190454932 | GTATGTA | G | 24 | a0001c0001t0001g0130 a0001c0001t0001g0231 a0001c0001t0001g0238 others(21): Show |
25 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1533-14763_1533-14 others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | ||||||
| chr2:190454932 | GTATGTAT others(5): Show |
G | 33 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0074 others(30): Show |
36 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1533-14769_1533-14 others(18): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | ||||||
| chr2:190454932 | GTATGTAT others(11): Show |
G | 14 | a0002c0002t0001g0008 a0002c0002t0001g0155 a0002c0002t0001g0164 others(11): Show |
15 | HG00609.hp2 HG00621.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.1533-14775_1533-14 others(24): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | ||||||
| chr2:190454932 | GTATGTAT others(17): Show |
G | 3 | a0002c0002t0001g0182 a0002c0002t0001g0183 a0002c0002t0001g0184 |
3 | HG00423.hp2 NA18965.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1533-14781_1533-14 others(30): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454932 | ||||||
| chr2:190454963 | TATGTATA others(30): Show |
T | 3 | a0001c0001t0003g0052 a0001c0001t0003g0058 a0001c0001t0003g0212 |
3 | HG01081.hp2 HG02602.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1533-14772_1533-14 others(43): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454963 | ||||||
| chr2:190454967 | T | C | 1 | a0002c0002t0003g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1533-14791T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190454967 | |||||||
| chr2:190454969 | TATGTATA others(24): Show |
T | 25 | a0001c0001t0002g0003 a0001c0001t0003g0013 a0001c0001t0003g0016 others(22): Show |
25 | HG00735.hp2 HG01070.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1533-14766_1533-14 others(37): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454969 | ||||||
| chr2:190454975 | TATGTATA others(18): Show |
T | 20 | a0001c0001t0002g0003 a0001c0001t0002g0071 a0001c0001t0002g0072 others(17): Show |
20 | HG00408.hp2 HG00741.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1533-14760_1533-14 others(31): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454975 | ||||||
| chr2:190454981 | TATGTATA others(12): Show |
T | 15 | a0001c0001t0002g0018 a0001c0001t0002g0131 a0001c0001t0002g0313 others(12): Show |
15 | HG00140.hp2 HG00323.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1533-14757_1533-14 others(25): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454981 | ||||||
| chr2:190454987 | TATGTATA others(6): Show |
T | 14 | a0001c0001t0002g0015 a0001c0001t0002g0070 a0001c0001t0002g0089 others(11): Show |
14 | HG00544.hp1 HG01515.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1533-14757_1533-14 others(19): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454987 | ||||||
| chr2:190454993 | TATGTATA | T | 31 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0014 others(28): Show |
35 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1533-14757_1533-14 others(13): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454993 | ||||||
| chr2:190454999 | TA | T | 11 | a0001c0001t0002g0079 a0001c0001t0002g0081 a0001c0001t0002g0083 others(8): Show |
11 | HG02027.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1533-14757delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190454999 | ||||||
| chr2:190455000 | A | ATGTAT | 14 | a0001c0001t0002g0088 a0001c0001t0002g0091 a0001c0001t0002g0095 others(11): Show |
14 | HG00558.hp1 HG01123.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1533-14758_1533-14 others(11): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455000 | |||||||
| chr2:190455000 | A | ATGTATAT others(4): Show |
6 | a0001c0001t0002g0080 a0001c0001t0002g0090 a0001c0001t0002g0096 others(3): Show |
6 | HG01433.hp1 HG02622.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1533-14758_1533-14 others(17): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455000 | |||||||
| chr2:190455000 | A | ATGTATAT others(10): Show |
2 | a0001c0001t0002g0121 a0002c0002t0001g0277 |
2 | HG00544.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1533-14758_1533-14 others(23): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455000 | |||||||
| chr2:190455044 | A | G | 1 | a0002c0002t0001g0263 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1533-14714A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455044 | |||||||
| chr2:190455198 | A | G | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1533-14560A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455198 | |||||||
| chr2:190455252 | A | G | 5 | a0002c0002t0001g0008 a0002c0002t0001g0182 a0002c0002t0001g0183 others(2): Show |
6 | HG00423.hp2 HG00609.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1533-14506A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455252 | |||||||
| chr2:190455253 | TTATTAC | T | 3 | a0002c0002t0008g0202 a0002c0002t0008g0211 a0002c0011t0001g0320 |
3 | HG01884.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-14499_1533-14 others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455253 | ||||||
| chr2:190455280 | TATTA | T | 62 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1533-14472_1533-14 others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455280 | ||||||
| chr2:190455377 | T | A | 4 | a0001c0001t0002g0129 a0001c0001t0002g0131 a0001c0001t0002g0132 others(1): Show |
4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533-14381T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455377 | |||||||
| chr2:190455452 | G | A | 14 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(11): Show |
14 | HG00323.hp1 HG00741.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1533-14306G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455452 | |||||||
| chr2:190455519 | A | T | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1533-14239A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190455519 | |||||||
| chr2:190455934 | C | CT | 98 | a0001c0001t0001g0130 a0001c0001t0001g0224 a0001c0001t0001g0226 others(95): Show |
101 | HG00558.hp2 HG00609.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1533-13800dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455934 | ||||||
| chr2:190455934 | C | CTT | 95 | a0001c0001t0001g0143 a0001c0001t0001g0225 a0001c0001t0001g0245 others(92): Show |
97 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1533-13801_1533-13 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455934 | ||||||
| chr2:190455934 | C | CTTT | 28 | a0001c0001t0002g0015 a0001c0001t0002g0094 a0001c0001t0003g0017 others(25): Show |
30 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1533-13802_1533-13 others(9): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455934 | ||||||
| chr2:190455934 | C | CTTTT | 67 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0069 others(64): Show |
72 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1533-13803_1533-13 others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455934 | ||||||
| chr2:190455934 | C | CTTTTT | 14 | a0001c0001t0001g0097 a0001c0001t0002g0083 a0001c0001t0002g0084 others(11): Show |
14 | HG00735.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1533-13804_1533-13 others(11): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190455934 | ||||||
| chr2:190456035 | G | C | 49 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0073 others(46): Show |
53 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1533-13723G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190456035 | |||||||
| chr2:190456417 | G | A | 8 | a0002c0002t0001g0147 a0002c0002t0001g0150 a0002c0002t0001g0164 others(5): Show |
8 | NA18960.hp1 NA18961.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.1533-13341G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190456417 | |||||||
| chr2:190456499 | T | TA | 3 | a0002c0002t0008g0202 a0002c0002t0008g0211 a0002c0011t0001g0320 |
3 | HG01884.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-13258dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190456499 | ||||||
| chr2:190456527 | C | T | 4 | a0001c0001t0002g0129 a0001c0001t0002g0131 a0001c0001t0002g0132 others(1): Show |
4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533-13231C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190456527 | |||||||
| chr2:190456632 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1533-13126C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190456632 | |||||||
| chr2:190456901 | G | T | 3 | a0002c0002t0008g0202 a0002c0002t0008g0211 a0002c0011t0001g0320 |
3 | HG01884.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-12857G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190456901 | |||||||
| chr2:190457000 | G | A | 62 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1533-12758G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457000 | |||||||
| chr2:190457071 | G | A | 62 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1533-12687G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457071 | |||||||
| chr2:190457178 | C | T | 160 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0003g0034 others(157): Show |
167 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.1533-12580C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457178 | |||||||
| chr2:190457251 | G | T | 1 | a0002c0002t0005g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1533-12507G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457251 | |||||||
| chr2:190457411 | C | A | 1 | a0001c0001t0002g0105 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1533-12347C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457411 | |||||||
| chr2:190457546 | G | C | 62 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1533-12212G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457546 | |||||||
| chr2:190457888 | C | A | 1 | a0002c0002t0001g0278 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1533-11870C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190457888 | |||||||
| chr2:190458167 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1533-11591G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458167 | |||||||
| chr2:190458194 | CCCTGAAG others(21): Show |
C | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1533-11561_1533-11 others(34): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190458194 | ||||||
| chr2:190458412 | C | T | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-11346C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458412 | |||||||
| chr2:190458457 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1533-11301T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458457 | |||||||
| chr2:190458464 | CTT | C | 150 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0002c0002t0001g0002 others(147): Show |
157 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.1533-11291_1533-11 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190458464 | ||||||
| chr2:190458569 | C | T | 80 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0003 others(77): Show |
85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1533-11189C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458569 | |||||||
| chr2:190458603 | C | T | 59 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0018 others(56): Show |
59 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1533-11155C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458603 | |||||||
| chr2:190458975 | A | G | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1533-10783A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190458975 | |||||||
| chr2:190459477 | G | T | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1533-10281G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190459477 | |||||||
| chr2:190459489 | A | T | 298 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(295): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1533-10269A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190459489 | |||||||
| chr2:190459490 | A | C | 4 | a0001c0001t0002g0129 a0001c0001t0002g0131 a0001c0001t0002g0132 others(1): Show |
4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533-10268A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190459490 | |||||||
| chr2:190459490 | A | G | 1 | a0002c0002t0001g0290 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1533-10268A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190459490 | |||||||
| chr2:190459932 | T | C | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1533-9826T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190459932 | |||||||
| chr2:190460163 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1533-9595G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460163 | |||||||
| chr2:190460235 | A | C | 6 | a0002c0002t0001g0165 a0002c0002t0001g0297 a0002c0002t0001g0298 others(3): Show |
6 | NA18944.hp1 NA18997.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-9523A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460235 | |||||||
| chr2:190460267 | G | A | 1 | a0001c0001t0003g0013 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1533-9491G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460267 | |||||||
| chr2:190460326 | T | C | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-9432T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460326 | |||||||
| chr2:190460446 | C | T | 2 | a0002c0002t0008g0202 a0002c0002t0008g0211 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-9312C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460446 | |||||||
| chr2:190460477 | G | A | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1533-9281G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460477 | |||||||
| chr2:190460498 | A | G | 6 | a0002c0002t0001g0165 a0002c0002t0001g0297 a0002c0002t0001g0298 others(3): Show |
6 | NA18944.hp1 NA18997.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-9260A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460498 | |||||||
| chr2:190460529 | C | G | 219 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0002g0014 others(216): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1533-9229C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460529 | |||||||
| chr2:190460676 | C | T | 1 | a0002c0002t0001g0204 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1533-9082C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460676 | |||||||
| chr2:190460688 | A | G | 82 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0003 others(79): Show |
87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1533-9070A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460688 | |||||||
| chr2:190460875 | A | C | 79 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0003 others(76): Show |
84 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1533-8883A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460875 | |||||||
| chr2:190460899 | A | C | 1 | a0002c0002t0001g0262 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1533-8859A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190460899 | |||||||
| chr2:190461601 | G | A | 151 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0002c0002t0001g0002 others(148): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.1533-8157G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190461601 | |||||||
| chr2:190461622 | A | G | 299 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533-8136A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190461622 | |||||||
| chr2:190461975 | C | T | 306 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(303): Show |
318 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.1533-7783C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190461975 | |||||||
| chr2:190462215 | G | T | 1 | a0001c0010t0002g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1533-7543G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462215 | |||||||
| chr2:190462421 | T | C | 82 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0003 others(79): Show |
87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1533-7337T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462421 | |||||||
| chr2:190462505 | C | T | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1533-7253C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462505 | |||||||
| chr2:190462545 | A | T | 1 | a0002c0002t0001g0307 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1533-7213A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462545 | |||||||
| chr2:190462785 | T | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1533-6973T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462785 | |||||||
| chr2:190462989 | G | C | 2 | a0002c0002t0008g0202 a0002c0002t0008g0211 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-6769G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190462989 | |||||||
| chr2:190463126 | A | G | 79 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0003 others(76): Show |
84 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1533-6632A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463126 | |||||||
| chr2:190463183 | G | C | 2 | a0001c0001t0002g0085 a0001c0001t0002g0134 |
2 | NA19004.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1533-6575G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463183 | |||||||
| chr2:190463314 | A | G | 1 | a0001c0001t0003g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1533-6444A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463314 | |||||||
| chr2:190463354 | T | C | 1 | a0002c0002t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1533-6404T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463354 | |||||||
| chr2:190463493 | T | A | 298 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(295): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1533-6265T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463493 | |||||||
| chr2:190463576 | T | C | 1 | a0002c0002t0008g0202 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1533-6182T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463576 | |||||||
| chr2:190463714 | G | T | 78 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0069 others(75): Show |
83 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1533-6044G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190463714 | |||||||
| chr2:190464454 | G | A | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1533-5304G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190464454 | |||||||
| chr2:190464642 | T | A | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1533-5116T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190464642 | |||||||
| chr2:190464680 | G | A | 99 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0002c0002t0001g0008 others(96): Show |
102 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.1533-5078G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190464680 | |||||||
| chr2:190464711 | T | C | 1 | a0001c0001t0003g0045 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1533-5047T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190464711 | |||||||
| chr2:190464903 | T | G | 9 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0024 others(6): Show |
9 | HG00735.hp2 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533-4855T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190464903 | |||||||
| chr2:190465063 | A | G | 299 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533-4695A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465063 | |||||||
| chr2:190465298 | T | C | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-4460T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465298 | |||||||
| chr2:190465425 | CT | C | 49 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0073 others(46): Show |
53 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1533-4324delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190465425 | ||||||
| chr2:190465436 | A | G | 196 | a0001c0001t0001g0143 a0001c0001t0002g0001 a0001c0001t0002g0003 others(193): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1533-4322A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465436 | |||||||
| chr2:190465571 | G | T | 59 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(56): Show |
59 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1533-4187G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465571 | |||||||
| chr2:190465630 | C | G | 6 | a0001c0001t0001g0097 a0002c0002t0001g0196 a0002c0002t0001g0201 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-4128C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465630 | |||||||
| chr2:190465632 | G | T | 151 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(148): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.1533-4126G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465632 | |||||||
| chr2:190465728 | C | CA | 14 | a0002c0002t0001g0002 a0002c0002t0001g0165 a0002c0002t0001g0176 others(11): Show |
16 | NA18941.hp2 NA18944.hp1 NA18955.hp1 others(13): Show |
intron_variant | MODIFIER | c.1533-4029dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190465728 | ||||||
| chr2:190465756 | G | T | 1 | a0001c0001t0018g0054 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1533-4002G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465756 | |||||||
| chr2:190465850 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1533-3908G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190465850 | |||||||
| chr2:190466004 | G | A | 2 | a0002c0002t0005g0187 a0002c0002t0005g0205 |
2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1533-3754G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466004 | |||||||
| chr2:190466060 | C | G | 163 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0003g0013 others(160): Show |
166 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1533-3698C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466060 | |||||||
| chr2:190466111 | C | T | 246 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0002g0001 others(243): Show |
254 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.1533-3647C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466111 | |||||||
| chr2:190466130 | G | T | 216 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(213): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1533-3628G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466130 | |||||||
| chr2:190466135 | A | T | 154 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(151): Show |
161 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.1533-3623A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466135 | |||||||
| chr2:190466301 | A | G | 299 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533-3457A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466301 | |||||||
| chr2:190466338 | A | G | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1533-3420A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466338 | |||||||
| chr2:190466407 | C | A | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-3351C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466407 | |||||||
| chr2:190466488 | C | T | 149 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(146): Show |
156 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.1533-3270C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466488 | |||||||
| chr2:190466578 | G | C | 78 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(75): Show |
83 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1533-3180G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466578 | |||||||
| chr2:190466658 | A | C | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-3100A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466658 | |||||||
| chr2:190466892 | G | A | 1 | a0001c0001t0023g0041 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1533-2866G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466892 | |||||||
| chr2:190466905 | C | G | 1 | a0002c0002t0008g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1533-2853C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466905 | |||||||
| chr2:190466925 | G | C | 1 | a0001c0001t0002g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1533-2833G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190466925 | |||||||
| chr2:190467321 | C | T | 2 | a0001c0001t0003g0022 a0001c0001t0003g0023 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1533-2437C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190467321 | |||||||
| chr2:190467376 | GC | G | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533-2380delC | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190467376 | ||||||
| chr2:190467443 | T | A | 87 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(84): Show |
92 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1533-2315T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190467443 | |||||||
| chr2:190467620 | G | T | 4 | a0002c0002t0001g0151 a0002c0002t0001g0175 a0002c0002t0001g0177 others(1): Show |
4 | HG00609.hp1 HG00621.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533-2138G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190467620 | |||||||
| chr2:190467914 | A | G | 2 | a0002c0002t0001g0201 a0002c0002t0001g0322 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1533-1844A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190467914 | |||||||
| chr2:190468011 | C | T | 8 | a0002c0002t0001g0165 a0002c0002t0001g0176 a0002c0002t0001g0180 others(5): Show |
8 | NA18944.hp1 NA18955.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.1533-1747C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190468011 | |||||||
| chr2:190468453 | A | AT | 60 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(57): Show |
60 | HG00408.hp2 HG00544.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1533-1288dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190468453 | ||||||
| chr2:190468453 | AT | A | 6 | a0001c0001t0001g0233 a0001c0001t0002g0095 a0001c0001t0002g0099 others(3): Show |
6 | HG01496.hp1 HG02451.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-1288delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190468453 | ||||||
| chr2:190468619 | A | AT | 9 | a0001c0001t0001g0148 a0001c0001t0001g0232 a0001c0001t0001g0233 others(6): Show |
9 | HG01361.hp1 HG01496.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1533-1120dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190468619 | ||||||
| chr2:190468619 | AT | A | 221 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(218): Show |
233 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1533-1120delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190468619 | ||||||
| chr2:190468619 | ATT | A | 9 | a0001c0001t0002g0117 a0002c0002t0001g0188 a0002c0002t0001g0204 others(6): Show |
9 | HG01515.hp1 HG02486.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533-1121_1533-112 others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190468619 | ||||||
| chr2:190468626 | T | A | 1 | a0002c0002t0001g0266 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1533-1132T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190468626 | |||||||
| chr2:190468647 | C | T | 2 | a0002c0002t0008g0202 a0002c0002t0008g0211 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-1111C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190468647 | |||||||
| chr2:190468807 | A | G | 299 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1533-951A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190468807 | |||||||
| chr2:190469002 | C | T | 211 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(208): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1533-756C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469002 | |||||||
| chr2:190469143 | T | C | 1 | a0002c0002t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1533-615T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469143 | |||||||
| chr2:190469305 | G | C | 100 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0002c0002t0001g0008 others(97): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1533-453G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469305 | |||||||
| chr2:190469310 | T | C | 1 | a0002c0002t0001g0177 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1533-448T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469310 | |||||||
| chr2:190469326 | T | A | 2 | a0002c0002t0008g0202 a0002c0002t0008g0211 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-432T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469326 | |||||||
| chr2:190469698 | G | A | 150 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(147): Show |
157 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.1533-60G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469698 | |||||||
| chr2:190469727 | T | A | 1 | a0002c0002t0004g0006 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1533-31T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469727 | |||||||
| chr2:190469733 | A | ATTTTTAT | 298 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(295): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
splice_region_variant&intron_variant | LOW | c.1533-12_1533-6dupA others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 190469733 | ||||||
| chr2:190469733 | A | T | 1 | a0002c0002t0001g0289 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1533-25A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 3/7 | chr2 | 190469733 | |||||||
| chr2:190469867 | G | T | 1 | a0005c0005t0001g0284 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1630+12G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190469867 | |||||||
| chr2:190470011 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1630+156G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470011 | |||||||
| chr2:190470232 | A | G | 1 | a0002c0002t0009g0296 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1630+377A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470232 | |||||||
| chr2:190470331 | T | C | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630+476T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470331 | |||||||
| chr2:190470357 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1630+502T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470357 | |||||||
| chr2:190470381 | T | A | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1630+526T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470381 | |||||||
| chr2:190470586 | C | T | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1630+731C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470586 | |||||||
| chr2:190470703 | G | A | 2 | a0002c0002t0005g0187 a0002c0002t0005g0205 |
2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1630+848G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470703 | |||||||
| chr2:190470757 | T | A | 60 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(57): Show |
60 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1630+902T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470757 | |||||||
| chr2:190470903 | G | GTA | 49 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0015 others(46): Show |
50 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1630+1061_1630+106 others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190470903 | ||||||
| chr2:190470903 | G | GTATA | 29 | a0001c0001t0002g0001 a0001c0001t0002g0076 a0001c0001t0002g0077 others(26): Show |
33 | HG00408.hp1 HG00423.hp1 HG02165.hp1 others(30): Show |
intron_variant | MODIFIER | c.1630+1059_1630+106 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190470903 | ||||||
| chr2:190470970 | A | G | 2 | a0001c0001t0021g0210 a0002c0011t0001g0320 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1630+1115A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190470970 | |||||||
| chr2:190471208 | G | A | 60 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(57): Show |
60 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1630+1353G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471208 | |||||||
| chr2:190471226 | A | C | 1 | a0001c0001t0003g0013 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1630+1371A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471226 | |||||||
| chr2:190471247 | G | C | 2 | a0002c0002t0001g0201 a0002c0002t0001g0322 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1630+1392G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471247 | |||||||
| chr2:190471288 | G | A | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1630+1433G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471288 | |||||||
| chr2:190471525 | C | T | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1630+1670C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471525 | |||||||
| chr2:190471596 | A | G | 1 | a0005c0005t0001g0284 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1630+1741A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471596 | |||||||
| chr2:190471717 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1630+1862T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471717 | |||||||
| chr2:190471812 | G | A | 6 | a0001c0001t0001g0097 a0002c0002t0001g0196 a0002c0002t0001g0201 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1630+1957G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471812 | |||||||
| chr2:190471904 | C | T | 2 | a0002c0002t0001g0269 a0002c0002t0001g0286 |
2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1630+2049C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471904 | |||||||
| chr2:190471973 | C | G | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630+2118C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190471973 | |||||||
| chr2:190472203 | G | A | 299 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1630+2348G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472203 | |||||||
| chr2:190472421 | C | T | 1 | a0001c0001t0012g0247 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1630+2566C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472421 | |||||||
| chr2:190472555 | C | T | 1 | a0002c0002t0003g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1630+2700C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472555 | |||||||
| chr2:190472622 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1630+2767G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472622 | |||||||
| chr2:190472692 | A | G | 3 | a0001c0001t0003g0034 a0001c0001t0003g0056 a0001c0001t0003g0057 |
3 | HG00735.hp2 HG01070.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1630+2837A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190472692 | |||||||
| chr2:190473272 | A | G | 1 | a0002c0002t0001g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1630+3417A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190473272 | |||||||
| chr2:190473490 | G | T | 62 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1630+3635G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190473490 | |||||||
| chr2:190473497 | G | A | 1 | a0001c0010t0002g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1630+3642G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190473497 | |||||||
| chr2:190473785 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1630+3930C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190473785 | |||||||
| chr2:190474131 | C | T | 1 | a0002c0002t0001g0262 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1630+4276C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474131 | |||||||
| chr2:190474159 | G | C | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630+4304G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474159 | |||||||
| chr2:190474173 | AAC | A | 59 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(56): Show |
59 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1630+4322_1630+432 others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190474173 | ||||||
| chr2:190474210 | A | T | 55 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(52): Show |
55 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1630+4355A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474210 | |||||||
| chr2:190474314 | G | A | 3 | a0001c0001t0002g0124 a0001c0001t0006g0004 a0001c0001t0006g0005 |
5 | NA18982.hp1 NA19002.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630+4459G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474314 | |||||||
| chr2:190474407 | A | G | 78 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(75): Show |
83 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1630+4552A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474407 | |||||||
| chr2:190474411 | A | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1630+4556A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474411 | |||||||
| chr2:190474682 | G | T | 1 | a0002c0002t0001g0191 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1630+4827G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474682 | |||||||
| chr2:190474791 | G | T | 1 | a0002c0002t0001g0273 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1630+4936G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474791 | |||||||
| chr2:190474797 | G | C | 149 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(146): Show |
154 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1630+4942G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474797 | |||||||
| chr2:190474876 | G | C | 1 | a0001c0001t0003g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1630+5021G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474876 | |||||||
| chr2:190474915 | T | C | 1 | a0002c0002t0005g0187 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1630+5060T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190474915 | |||||||
| chr2:190475169 | C | G | 74 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(71): Show |
79 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1630+5314C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475169 | |||||||
| chr2:190475537 | A | G | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1630+5682A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475537 | |||||||
| chr2:190475670 | G | C | 4 | a0001c0001t0001g0097 a0002c0002t0001g0196 a0002c0002t0001g0206 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630+5815G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475670 | |||||||
| chr2:190475725 | C | T | 1 | a0002c0002t0001g0203 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1630+5870C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475725 | |||||||
| chr2:190475821 | C | G | 1 | a0002c0002t0005g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1630+5966C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475821 | |||||||
| chr2:190475937 | A | G | 1 | a0002c0002t0008g0202 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1630+6082A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190475937 | |||||||
| chr2:190476114 | A | G | 100 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0002c0002t0001g0008 others(97): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1630+6259A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476114 | |||||||
| chr2:190476160 | T | G | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1630+6305T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476160 | |||||||
| chr2:190476298 | A | G | 49 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0073 others(46): Show |
53 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1630+6443A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476298 | |||||||
| chr2:190476346 | C | G | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1630+6491C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476346 | |||||||
| chr2:190476469 | G | C | 55 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(52): Show |
55 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1630+6614G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476469 | |||||||
| chr2:190476528 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1630+6673G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476528 | |||||||
| chr2:190476529 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1630+6674G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476529 | |||||||
| chr2:190476640 | G | C | 100 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0002c0002t0001g0008 others(97): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1630+6785G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476640 | |||||||
| chr2:190476646 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1630+6791C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476646 | |||||||
| chr2:190476774 | A | G | 1 | a0001c0001t0003g0013 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1630+6919A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476774 | |||||||
| chr2:190476777 | C | A | 2 | a0001c0001t0002g0080 a0001c0001t0002g0090 |
2 | NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1630+6922C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476777 | |||||||
| chr2:190476852 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1630+6997C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476852 | |||||||
| chr2:190476876 | A | C | 1 | a0002c0002t0001g0262 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1630+7021A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190476876 | |||||||
| chr2:190477035 | C | T | 4 | a0001c0001t0001g0097 a0002c0002t0001g0196 a0002c0002t0001g0206 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1630+7180C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477035 | |||||||
| chr2:190477101 | GT | G | 4 | a0001c0001t0002g0129 a0001c0001t0002g0131 a0001c0001t0002g0132 others(1): Show |
4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630+7248delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190477101 | ||||||
| chr2:190477145 | G | A | 1 | a0002c0002t0001g0009 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1630+7290G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477145 | |||||||
| chr2:190477151 | A | G | 2 | a0002c0002t0008g0202 a0002c0002t0008g0211 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1630+7296A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477151 | |||||||
| chr2:190477199 | TATA | T | 8 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(5): Show |
8 | HG01099.hp1 HG01123.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1630+7358_1630+736 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190477199 | ||||||
| chr2:190477218 | A | G | 60 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(57): Show |
60 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1630+7363A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477218 | |||||||
| chr2:190477487 | G | T | 1 | a0006c0008t0003g0028 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1630+7632G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477487 | |||||||
| chr2:190477491 | C | G | 2 | a0002c0002t0001g0254 a0002c0002t0001g0266 |
2 | HG01261.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1630+7636C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477491 | |||||||
| chr2:190477606 | A | G | 1 | a0001c0001t0003g0024 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1630+7751A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477606 | |||||||
| chr2:190477671 | C | G | 2 | a0001c0001t0003g0019 a0001c0001t0003g0061 |
2 | NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1630+7816C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477671 | |||||||
| chr2:190477684 | A | C | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1630+7829A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477684 | |||||||
| chr2:190477703 | A | C | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630+7848A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477703 | |||||||
| chr2:190477739 | C | T | 2 | a0002c0011t0001g0320 a0008c0009t0015g0208 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1630+7884C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477739 | |||||||
| chr2:190477946 | TG | T | 56 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(53): Show |
56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.1630+8096delG | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190477946 | ||||||
| chr2:190477989 | G | A | 100 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0002c0002t0001g0008 others(97): Show |
103 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.1630+8134G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190477989 | |||||||
| chr2:190478001 | A | G | 1 | a0002c0002t0001g0195 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1630+8146A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478001 | |||||||
| chr2:190478112 | T | A | 2 | a0002c0002t0008g0202 a0002c0002t0008g0211 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1630+8257T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478112 | |||||||
| chr2:190478172 | G | A | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630+8317G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478172 | |||||||
| chr2:190478214 | T | G | 1 | a0003c0003t0010g0331 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1630+8359T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478214 | |||||||
| chr2:190478384 | A | C | 1 | a0001c0001t0016g0114 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1630+8529A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478384 | |||||||
| chr2:190478442 | T | G | 1 | a0001c0001t0003g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1630+8587T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478442 | |||||||
| chr2:190478599 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1630+8744G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478599 | |||||||
| chr2:190478728 | A | AGGCTGGG others(9): Show |
1 | a0002c0002t0001g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1630+8875_1630+889 others(20): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190478728 | ||||||
| chr2:190478835 | T | TA | 298 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(295): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1630+8990dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190478835 | ||||||
| chr2:190478980 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1630+9125C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190478980 | |||||||
| chr2:190479011 | T | C | 1 | a0002c0002t0001g0268 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1630+9156T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479011 | |||||||
| chr2:190479037 | T | C | 151 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(148): Show |
158 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.1630+9182T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479037 | |||||||
| chr2:190479087 | A | T | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1630+9232A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479087 | |||||||
| chr2:190479406 | C | T | 101 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0007t0001g0035 others(98): Show |
104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1631-9251C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479406 | |||||||
| chr2:190479511 | C | G | 1 | a0002c0002t0001g0290 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1631-9146C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479511 | |||||||
| chr2:190479522 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1631-9135T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479522 | |||||||
| chr2:190479602 | G | A | 1 | a0005c0005t0001g0284 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1631-9055G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479602 | |||||||
| chr2:190479807 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1631-8850C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479807 | |||||||
| chr2:190479823 | A | G | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-8834A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479823 | |||||||
| chr2:190479910 | G | A | 4 | a0002c0002t0001g0278 a0002c0002t0001g0285 a0002c0002t0001g0310 others(1): Show |
4 | NA18965.hp2 NA19058.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1631-8747G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479910 | |||||||
| chr2:190479916 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1631-8741C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190479916 | |||||||
| chr2:190480025 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1631-8632T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480025 | |||||||
| chr2:190480052 | A | T | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1631-8605A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480052 | |||||||
| chr2:190480161 | T | C | 57 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(54): Show |
57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1631-8496T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480161 | |||||||
| chr2:190480380 | ATAGT | A | 101 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0007t0001g0035 others(98): Show |
104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1631-8272_1631-826 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190480380 | ||||||
| chr2:190480443 | T | A | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1631-8214T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480443 | |||||||
| chr2:190480518 | C | T | 54 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(51): Show |
54 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1631-8139C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480518 | |||||||
| chr2:190480548 | T | A | 299 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1631-8109T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480548 | |||||||
| chr2:190480771 | A | G | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1631-7886A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480771 | |||||||
| chr2:190480820 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1631-7837A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190480820 | |||||||
| chr2:190481277 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1631-7380T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481277 | |||||||
| chr2:190481356 | C | T | 9 | a0001c0001t0003g0031 a0001c0001t0003g0038 a0001c0001t0003g0040 others(6): Show |
9 | NA18947.hp1 NA18949.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.1631-7301C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481356 | |||||||
| chr2:190481440 | C | T | 57 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(54): Show |
57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1631-7217C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481440 | |||||||
| chr2:190481567 | G | A | 51 | a0001c0001t0001g0143 a0001c0001t0021g0210 a0002c0002t0001g0002 others(48): Show |
55 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1631-7090G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481567 | |||||||
| chr2:190481673 | T | C | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1631-6984T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481673 | |||||||
| chr2:190481713 | A | G | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1631-6944A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481713 | |||||||
| chr2:190481811 | T | C | 2 | a0002c0002t0001g0123 a0002c0002t0001g0145 |
2 | NA18946.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1631-6846T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190481811 | |||||||
| chr2:190482058 | TAGG | T | 104 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0007t0001g0035 others(101): Show |
107 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1631-6594_1631-659 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482058 | ||||||
| chr2:190482076 | C | T | 5 | a0001c0001t0001g0097 a0002c0002t0001g0192 a0002c0002t0001g0196 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1631-6581C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482076 | |||||||
| chr2:190482109 | T | G | 1 | a0001c0001t0002g0133 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1631-6548T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482109 | |||||||
| chr2:190482157 | G | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0227 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1631-6500G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482157 | |||||||
| chr2:190482399 | CT | C | 6 | a0001c0001t0001g0230 a0001c0001t0002g0091 a0001c0001t0002g0095 others(3): Show |
6 | HG01255.hp1 HG01256.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1631-6243delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482399 | ||||||
| chr2:190482458 | G | A | 141 | a0001c0001t0001g0143 a0001c0001t0002g0001 a0001c0001t0002g0003 others(138): Show |
150 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1631-6199G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482458 | |||||||
| chr2:190482554 | A | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1631-6103A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482554 | |||||||
| chr2:190482584 | G | T | 101 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0007t0001g0035 others(98): Show |
104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1631-6073G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482584 | |||||||
| chr2:190482672 | CT | C | 84 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(81): Show |
89 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1631-5978delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482672 | ||||||
| chr2:190482719 | G | A | 1 | a0003c0003t0010g0330 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1631-5938G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482719 | |||||||
| chr2:190482770 | G | A | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1631-5887G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482770 | |||||||
| chr2:190482868 | C | CT | 6 | a0001c0001t0001g0234 a0001c0001t0001g0239 a0001c0001t0001g0240 others(3): Show |
6 | HG01192.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1631-5754dupT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | ||||||
| chr2:190482868 | CT | C | 11 | a0001c0001t0001g0221 a0001c0001t0001g0232 a0001c0001t0001g0235 others(8): Show |
11 | HG01361.hp1 HG02145.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1631-5754delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | ||||||
| chr2:190482868 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0002g0111 a0001c0001t0021g0210 |
2 | HG01099.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1631-5764_1631-575 others(15): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | ||||||
| chr2:190482868 | CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0001g0146 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1631-5768_1631-575 others(19): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | ||||||
| chr2:190482868 | CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0002g0099 |
3 | HG02451.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1631-5770_1631-575 others(21): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | ||||||
| chr2:190482868 | CTTTTTTT others(15): Show |
C | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-5775_1631-575 others(26): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190482868 | ||||||
| chr2:190482903 | T | G | 71 | a0001c0001t0001g0143 a0001c0001t0002g0070 a0001c0001t0002g0099 others(68): Show |
75 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1631-5754T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTG | 39 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0133 others(36): Show |
40 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(8): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTG | 35 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 others(32): Show |
36 | HG00609.hp2 HG00741.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(9): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTG | 42 | a0001c0001t0002g0100 a0001c0001t0002g0137 a0001c0001t0002g0223 others(39): Show |
43 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(10): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTG | 30 | a0001c0001t0002g0079 a0001c0001t0002g0327 a0001c0001t0003g0017 others(27): Show |
30 | HG01069.hp1 HG01074.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(11): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(1): Show |
10 | a0001c0001t0002g0071 a0001c0001t0002g0313 a0001c0001t0003g0023 others(7): Show |
10 | HG00544.hp1 HG01074.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(12): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(2): Show |
18 | a0001c0001t0001g0097 a0001c0001t0002g0001 a0001c0001t0002g0072 others(15): Show |
20 | HG00323.hp1 HG00408.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(13): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(3): Show |
22 | a0001c0001t0001g0130 a0001c0001t0002g0014 a0001c0001t0002g0069 others(19): Show |
23 | HG00735.hp2 HG01243.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(14): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(4): Show |
11 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0106 others(8): Show |
13 | HG02027.hp1 HG02071.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(15): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(5): Show |
3 | a0001c0001t0003g0029 a0001c0001t0003g0049 a0002c0002t0001g0196 |
3 | HG00323.hp2 HG02615.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(16): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(6): Show |
3 | a0001c0001t0002g0125 a0001c0001t0003g0055 a0002c0002t0001g0329 |
3 | HG00140.hp2 HG02055.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(17): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(7): Show |
3 | a0001c0001t0002g0078 a0001c0001t0002g0080 a0001c0001t0002g0090 |
3 | NA18969.hp2 NA18988.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(18): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(8): Show |
1 | a0001c0001t0002g0084 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1631-5754_1631-575 others(19): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(9): Show |
2 | a0001c0001t0002g0018 a0002c0002t0001g0206 |
2 | HG01891.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(20): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(10): Show |
1 | a0001c0001t0002g0082 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1631-5754_1631-575 others(21): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(14): Show |
1 | a0001c0001t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1631-5754_1631-575 others(25): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(17): Show |
3 | a0001c0001t0002g0102 a0001c0001t0002g0108 a0001c0001t0002g0109 |
3 | NA18941.hp1 NA18942.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1631-5754_1631-575 others(28): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482903 | T | TTTTTTTT others(18): Show |
1 | a0001c0001t0002g0110 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1631-5754_1631-575 others(29): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482903 | |||||||
| chr2:190482932 | C | T | 1 | a0002c0002t0001g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1631-5725C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482932 | |||||||
| chr2:190482939 | C | A | 1 | a0001c0001t0002g0125 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1631-5718C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482939 | |||||||
| chr2:190482940 | G | A | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-5717G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190482940 | |||||||
| chr2:190483037 | G | A | 4 | a0001c0001t0002g0129 a0001c0001t0002g0131 a0001c0001t0002g0132 others(1): Show |
4 | HG01106.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1631-5620G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483037 | |||||||
| chr2:190483047 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1631-5610G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483047 | |||||||
| chr2:190483083 | G | A | 52 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(49): Show |
56 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1631-5574G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483083 | |||||||
| chr2:190483171 | C | T | 1 | a0006c0008t0003g0028 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1631-5486C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483171 | |||||||
| chr2:190483283 | A | G | 2 | a0001c0001t0021g0210 a0002c0011t0001g0320 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1631-5374A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483283 | |||||||
| chr2:190483350 | C | A | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-5307C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483350 | |||||||
| chr2:190483619 | G | C | 78 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(75): Show |
83 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1631-5038G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483619 | |||||||
| chr2:190483696 | G | A | 3 | a0002c0002t0001g0146 a0002c0002t0008g0202 a0002c0002t0008g0211 |
3 | HG01255.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1631-4961G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483696 | |||||||
| chr2:190483775 | C | T | 1 | a0002c0002t0001g0329 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1631-4882C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190483775 | |||||||
| chr2:190483835 | C | CA | 68 | a0001c0001t0002g0111 a0002c0002t0001g0010 a0002c0002t0001g0127 others(65): Show |
69 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.1631-4801dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190483835 | ||||||
| chr2:190483835 | CA | C | 11 | a0001c0001t0002g0109 a0001c0001t0002g0117 a0001c0001t0002g0144 others(8): Show |
11 | HG01168.hp2 HG01515.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1631-4801delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190483835 | ||||||
| chr2:190483835 | CAAA | C | 32 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0007t0001g0035 others(29): Show |
34 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1631-4803_1631-480 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190483835 | ||||||
| chr2:190484027 | T | G | 117 | a0001c0001t0001g0097 a0001c0001t0001g0148 a0001c0001t0001g0221 others(114): Show |
122 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1631-4630T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484027 | |||||||
| chr2:190484345 | T | A | 27 | a0001c0001t0001g0130 a0001c0007t0001g0035 a0002c0002t0001g0008 others(24): Show |
29 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1631-4312T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484345 | |||||||
| chr2:190484351 | A | G | 60 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(57): Show |
60 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1631-4306A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484351 | |||||||
| chr2:190484436 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1631-4221A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484436 | |||||||
| chr2:190484646 | T | A | 1 | a0001c0001t0002g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1631-4011T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484646 | |||||||
| chr2:190484746 | T | G | 3 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0137 |
3 | HG02145.hp1 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1631-3911T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484746 | |||||||
| chr2:190484802 | G | C | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1631-3855G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484802 | |||||||
| chr2:190484956 | T | G | 298 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(295): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1631-3701T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484956 | |||||||
| chr2:190484957 | C | G | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-3700C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190484957 | |||||||
| chr2:190485274 | T | A | 3 | a0001c0001t0008g0332 a0002c0002t0008g0202 a0002c0002t0008g0211 |
3 | HG03471.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1631-3383T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485274 | |||||||
| chr2:190485661 | T | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1631-2996T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485661 | |||||||
| chr2:190485703 | G | A | 57 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(54): Show |
57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1631-2954G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485703 | |||||||
| chr2:190485803 | TA | T | 103 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0002g0079 others(100): Show |
107 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1631-2840delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190485803 | ||||||
| chr2:190485819 | C | A | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2838C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485819 | |||||||
| chr2:190485852 | C | A | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2805C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485852 | |||||||
| chr2:190485855 | A | T | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2802A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485855 | |||||||
| chr2:190485856 | A | T | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2801A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485856 | |||||||
| chr2:190485857 | G | A | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2800G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485857 | |||||||
| chr2:190485858 | A | G | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-2799A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190485858 | |||||||
| chr2:190486251 | G | A | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1631-2406G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190486251 | |||||||
| chr2:190486293 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1631-2364G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190486293 | |||||||
| chr2:190486410 | C | A | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-2247C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190486410 | |||||||
| chr2:190486432 | G | A | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1631-2225G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190486432 | |||||||
| chr2:190486969 | T | A | 1 | a0002c0002t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1631-1688T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190486969 | |||||||
| chr2:190487015 | T | C | 235 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(232): Show |
247 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1631-1642T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487015 | |||||||
| chr2:190487172 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1631-1485C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487172 | |||||||
| chr2:190487198 | G | A | 9 | a0001c0001t0003g0031 a0001c0001t0003g0038 a0001c0001t0003g0040 others(6): Show |
9 | NA18947.hp1 NA18949.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.1631-1459G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487198 | |||||||
| chr2:190487209 | C | G | 82 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(79): Show |
87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1631-1448C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487209 | |||||||
| chr2:190487209 | C | T | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1631-1448C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487209 | |||||||
| chr2:190487239 | G | T | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-1418G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487239 | |||||||
| chr2:190487253 | A | T | 1 | a0001c0001t0003g0024 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1631-1404A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487253 | |||||||
| chr2:190487517 | G | A | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-1140G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487517 | |||||||
| chr2:190487518 | A | T | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-1139A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487518 | |||||||
| chr2:190487519 | T | G | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-1138T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487519 | |||||||
| chr2:190487613 | AAAG | A | 3 | a0002c0002t0001g0253 a0002c0002t0001g0255 a0002c0002t0001g0283 |
3 | NA18953.hp1 NA18967.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1631-1039_1631-103 others(7): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190487613 | ||||||
| chr2:190487903 | AT | A | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-745delT | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 190487903 | ||||||
| chr2:190487906 | T | A | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-751T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487906 | |||||||
| chr2:190487914 | T | C | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-743T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487914 | |||||||
| chr2:190487998 | G | T | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-659G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190487998 | |||||||
| chr2:190488000 | T | C | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-657T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488000 | |||||||
| chr2:190488001 | C | A | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-656C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488001 | |||||||
| chr2:190488028 | G | A | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1631-629G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488028 | |||||||
| chr2:190488047 | C | T | 2 | a0001c0007t0001g0035 a0002c0002t0001g0195 |
2 | NA18986.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1631-610C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488047 | |||||||
| chr2:190488059 | C | T | 1 | a0001c0001t0003g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1631-598C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488059 | |||||||
| chr2:190488128 | C | A | 1 | a0002c0002t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1631-529C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488128 | |||||||
| chr2:190488148 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1631-509G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488148 | |||||||
| chr2:190488162 | A | C | 1 | a0002c0002t0001g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1631-495A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488162 | |||||||
| chr2:190488190 | T | C | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1631-467T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488190 | |||||||
| chr2:190488240 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1631-417A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488240 | |||||||
| chr2:190488282 | A | G | 1 | a0001c0001t0003g0212 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1631-375A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488282 | |||||||
| chr2:190488403 | A | G | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1631-254A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488403 | |||||||
| chr2:190488501 | C | T | 2 | a0003c0003t0010g0330 a0003c0003t0010g0331 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1631-156C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488501 | |||||||
| chr2:190488510 | A | T | 1 | a0002c0002t0004g0213 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1631-147A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488510 | |||||||
| chr2:190488646 | T | C | 1 | a0002c0002t0001g0161 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1631-11T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 4/7 | chr2 | 190488646 | |||||||
| chr2:190489335 | T | G | 1 | a0001c0001t0008g0332 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1793-433T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489335 | |||||||
| chr2:190489446 | A | G | 2 | a0002c0002t0008g0202 a0002c0002t0008g0211 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1793-322A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489446 | |||||||
| chr2:190489471 | T | C | 1 | a0001c0001t0003g0042 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1793-297T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489471 | |||||||
| chr2:190489499 | A | T | 1 | a0002c0002t0008g0202 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1793-269A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489499 | |||||||
| chr2:190489574 | T | C | 1 | a0001c0001t0012g0247 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1793-194T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489574 | |||||||
| chr2:190489698 | C | T | 6 | a0001c0001t0008g0332 a0002c0002t0008g0202 a0002c0002t0008g0211 others(3): Show |
6 | HG03195.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1793-70C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489698 | |||||||
| chr2:190489703 | G | A | 1 | a0002c0002t0001g0283 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1793-65G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489703 | |||||||
| chr2:190489765 | T | C | 101 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0007t0001g0035 others(98): Show |
104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
splice_region_variant&intron_variant | LOW | c.1793-3T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 5/7 | chr2 | 190489765 | |||||||
| chr2:190489932 | C | CCT | 299 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1891+66_1891+67ins others(2): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190489932 | |||||||
| chr2:190490097 | GTT | G | 54 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(51): Show |
54 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1891+234_1891+235d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190490097 | ||||||
| chr2:190490237 | C | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(80): Show |
88 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1891+371C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490237 | |||||||
| chr2:190490245 | T | C | 1 | a0002c0002t0001g0292 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1891+379T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490245 | |||||||
| chr2:190490257 | A | G | 2 | a0001c0001t0002g0116 a0001c0001t0016g0114 |
2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1891+391A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490257 | |||||||
| chr2:190490263 | T | TA | 7 | a0002c0002t0001g0002 a0002c0002t0001g0179 a0002c0002t0001g0197 others(4): Show |
9 | HG01884.hp2 HG02559.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1891+411dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190490263 | ||||||
| chr2:190490263 | TA | T | 62 | a0001c0001t0001g0234 a0001c0001t0002g0144 a0001c0001t0003g0013 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1891+411delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190490263 | ||||||
| chr2:190490307 | T | C | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1891+441T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490307 | |||||||
| chr2:190490334 | C | T | 1 | a0002c0002t0001g0312 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1891+468C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490334 | |||||||
| chr2:190490562 | C | CA | 51 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(48): Show |
55 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1891+706dupA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190490562 | ||||||
| chr2:190490655 | C | A | 71 | a0001c0001t0001g0222 a0001c0001t0001g0225 a0001c0001t0001g0226 others(68): Show |
71 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1891+789C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490655 | |||||||
| chr2:190490807 | G | A | 9 | a0001c0001t0001g0148 a0001c0001t0001g0231 a0001c0001t0001g0232 others(6): Show |
9 | HG01361.hp1 HG01496.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1891+941G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490807 | |||||||
| chr2:190490889 | T | A | 3 | a0001c0001t0003g0026 a0001c0001t0003g0042 a0001c0001t0003g0048 |
3 | HG00544.hp1 NA18962.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1891+1023T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190490889 | |||||||
| chr2:190491574 | C | T | 299 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1891+1708C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190491574 | |||||||
| chr2:190491940 | A | G | 2 | a0002c0002t0001g0201 a0002c0002t0001g0322 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1891+2074A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190491940 | |||||||
| chr2:190491994 | C | T | 5 | a0002c0002t0005g0149 a0002c0002t0005g0187 a0002c0002t0005g0200 others(2): Show |
5 | HG02258.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1891+2128C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190491994 | |||||||
| chr2:190492017 | C | G | 1 | a0001c0001t0002g0094 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1891+2151C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492017 | |||||||
| chr2:190492061 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1891+2195T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492061 | |||||||
| chr2:190492103 | A | G | 6 | a0001c0001t0008g0332 a0002c0002t0008g0202 a0002c0002t0008g0211 others(3): Show |
6 | HG03195.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1891+2237A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492103 | |||||||
| chr2:190492123 | A | G | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0014 others(80): Show |
88 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1891+2257A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492123 | |||||||
| chr2:190492561 | A | G | 1 | a0002c0011t0001g0320 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1891+2695A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492561 | |||||||
| chr2:190492762 | C | CACTACCA others(16): Show |
2 | a0001c0001t0001g0238 a0001c0001t0001g0250 |
2 | HG01192.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1891+2933_1891+295 others(27): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190492762 | ||||||
| chr2:190492822 | A | C | 1 | a0002c0002t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1891+2956A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492822 | |||||||
| chr2:190492826 | A | C | 1 | a0002c0002t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1891+2960A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492826 | |||||||
| chr2:190492968 | A | T | 158 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(155): Show |
165 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.1891+3102A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190492968 | |||||||
| chr2:190493036 | C | T | 1 | a0002c0002t0001g0198 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1891+3170C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493036 | |||||||
| chr2:190493074 | A | C | 1 | a0002c0002t0001g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1891+3208A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493074 | |||||||
| chr2:190493143 | A | G | 234 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(231): Show |
246 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.1891+3277A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493143 | |||||||
| chr2:190493414 | T | C | 6 | a0002c0002t0001g0008 a0002c0002t0001g0182 a0002c0002t0001g0183 others(3): Show |
7 | HG00423.hp2 HG00609.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1891+3548T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493414 | |||||||
| chr2:190493441 | G | A | 101 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0007t0001g0035 others(98): Show |
104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1891+3575G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493441 | |||||||
| chr2:190493571 | G | T | 2 | a0001c0001t0011g0037 a0001c0001t0011g0043 |
2 | HG00408.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1891+3705G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493571 | |||||||
| chr2:190493685 | A | G | 3 | a0001c0001t0002g0124 a0001c0001t0006g0004 a0001c0001t0006g0005 |
5 | NA18982.hp1 NA19002.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.1892-3754A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493685 | |||||||
| chr2:190493720 | C | A | 1 | a0002c0002t0001g0319 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1892-3719C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493720 | |||||||
| chr2:190493771 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1892-3668T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493771 | |||||||
| chr2:190493787 | A | C | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-3652A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493787 | |||||||
| chr2:190493885 | T | C | 68 | a0002c0002t0001g0010 a0002c0002t0001g0123 a0002c0002t0001g0127 others(65): Show |
69 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.1892-3554T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190493885 | |||||||
| chr2:190494010 | G | C | 1 | a0003c0003t0022g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1892-3429G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494010 | |||||||
| chr2:190494062 | A | T | 1 | a0001c0001t0021g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1892-3377A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494062 | |||||||
| chr2:190494198 | C | T | 57 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(54): Show |
57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1892-3241C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494198 | |||||||
| chr2:190494253 | C | G | 101 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0007t0001g0035 others(98): Show |
104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1892-3186C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494253 | |||||||
| chr2:190494289 | T | C | 68 | a0002c0002t0001g0010 a0002c0002t0001g0123 a0002c0002t0001g0127 others(65): Show |
69 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.1892-3150T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494289 | |||||||
| chr2:190494425 | GA | G | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-3012delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190494425 | ||||||
| chr2:190494829 | C | T | 5 | a0002c0002t0001g0196 a0002c0002t0001g0201 a0002c0002t0001g0206 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1892-2610C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190494829 | |||||||
| chr2:190495018 | G | A | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0229 others(3): Show |
6 | HG01261.hp1 HG02886.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1892-2421G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495018 | |||||||
| chr2:190495063 | G | A | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-2376G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495063 | |||||||
| chr2:190495082 | A | T | 3 | a0001c0001t0008g0332 a0002c0002t0008g0202 a0002c0002t0008g0211 |
3 | HG03471.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1892-2357A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495082 | |||||||
| chr2:190495199 | A | AC | 68 | a0002c0002t0001g0010 a0002c0002t0001g0123 a0002c0002t0001g0127 others(65): Show |
69 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.1892-2238dupC | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190495199 | ||||||
| chr2:190495368 | C | T | 241 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(238): Show |
253 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1892-2071C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495368 | |||||||
| chr2:190495426 | A | C | 13 | a0002c0002t0001g0002 a0002c0002t0001g0176 a0002c0002t0001g0179 others(10): Show |
15 | NA18941.hp2 NA18944.hp1 NA18955.hp1 others(12): Show |
intron_variant | MODIFIER | c.1892-2013A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495426 | |||||||
| chr2:190495612 | A | G | 4 | a0001c0001t0003g0033 a0001c0001t0003g0036 a0001c0001t0003g0045 others(1): Show |
4 | NA18942.hp1 NA18944.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1892-1827A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495612 | |||||||
| chr2:190495736 | AG | A | 9 | a0001c0001t0003g0031 a0001c0001t0003g0038 a0001c0001t0003g0040 others(6): Show |
9 | NA18947.hp1 NA18949.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.1892-1698delG | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190495736 | ||||||
| chr2:190495745 | G | A | 9 | a0001c0001t0003g0031 a0001c0001t0003g0038 a0001c0001t0003g0040 others(6): Show |
9 | NA18947.hp1 NA18949.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.1892-1694G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495745 | |||||||
| chr2:190495826 | G | T | 299 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.1892-1613G>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495826 | |||||||
| chr2:190495840 | A | C | 59 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(56): Show |
59 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1892-1599A>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495840 | |||||||
| chr2:190495860 | T | A | 1 | a0002c0002t0001g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1892-1579T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495860 | |||||||
| chr2:190495916 | T | C | 101 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0007t0001g0035 others(98): Show |
104 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.1892-1523T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495916 | |||||||
| chr2:190495942 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1892-1497G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190495942 | |||||||
| chr2:190496028 | A | G | 3 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0088 |
3 | HG00423.hp1 HG02165.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1892-1411A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496028 | |||||||
| chr2:190496122 | C | G | 3 | a0001c0001t0008g0332 a0002c0002t0008g0202 a0002c0002t0008g0211 |
3 | HG03471.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1892-1317C>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496122 | |||||||
| chr2:190496143 | GA | G | 8 | a0001c0001t0003g0033 a0001c0001t0003g0036 a0001c0001t0003g0045 others(5): Show |
8 | HG03195.hp2 HG03453.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.1892-1285delA | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190496143 | ||||||
| chr2:190496218 | C | A | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1892-1221C>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496218 | |||||||
| chr2:190496231 | A | G | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-1208A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496231 | |||||||
| chr2:190496254 | G | C | 1 | a0003c0003t0022g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1892-1185G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496254 | |||||||
| chr2:190496522 | C | T | 57 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(54): Show |
57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1892-917C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496522 | |||||||
| chr2:190496611 | A | G | 1 | a0001c0001t0003g0046 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1892-828A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496611 | |||||||
| chr2:190496658 | ATGTG | A | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-775_1892-772d others(6): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190496658 | ||||||
| chr2:190496678 | G | GTA | 3 | a0001c0001t0008g0332 a0002c0002t0008g0202 a0002c0002t0008g0211 |
3 | HG03471.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1892-756_1892-755d others(4): Show |
MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 190496678 | ||||||
| chr2:190496779 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1892-660G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496779 | |||||||
| chr2:190496824 | A | G | 54 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(51): Show |
54 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1892-615A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190496824 | |||||||
| chr2:190497018 | C | T | 214 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0001g0143 others(211): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.1892-421C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497018 | |||||||
| chr2:190497071 | A | T | 1 | a0001c0001t0003g0063 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1892-368A>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497071 | |||||||
| chr2:190497107 | G | A | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1892-332G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497107 | |||||||
| chr2:190497132 | T | C | 3 | a0001c0001t0007g0011 a0001c0001t0007g0012 a0001c0001t0007g0142 |
3 | HG02630.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1892-307T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497132 | |||||||
| chr2:190497161 | A | G | 1 | a0002c0002t0003g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1892-278A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497161 | |||||||
| chr2:190497198 | T | A | 1 | a0008c0009t0015g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1892-241T>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 6/7 | chr2 | 190497198 | |||||||
| chr2:190497827 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2172+108G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190497827 | |||||||
| chr2:190497862 | T | G | 2 | a0002c0002t0008g0202 a0002c0002t0008g0211 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2172+143T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190497862 | |||||||
| chr2:190497931 | C | T | 1 | a0002c0002t0001g0074 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2172+212C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190497931 | |||||||
| chr2:190498051 | A | G | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0237 |
3 | HG01496.hp1 HG03942.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2172+332A>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190498051 | |||||||
| chr2:190498266 | T | G | 1 | a0001c0001t0003g0026 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2172+547T>G | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190498266 | |||||||
| chr2:190498482 | G | C | 2 | a0001c0001t0003g0032 a0001c0001t0003g0065 |
2 | HG02698.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2172+763G>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190498482 | |||||||
| chr2:190498770 | T | C | 58 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(55): Show |
58 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.2172+1051T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190498770 | |||||||
| chr2:190498826 | C | T | 1 | a0002c0002t0001g0267 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2172+1107C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190498826 | |||||||
| chr2:190499134 | T | C | 6 | a0001c0001t0008g0332 a0002c0002t0008g0202 a0002c0002t0008g0211 others(3): Show |
6 | HG03195.hp2 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2173-881T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190499134 | |||||||
| chr2:190499583 | C | T | 50 | a0001c0001t0001g0143 a0002c0002t0001g0002 a0002c0002t0001g0007 others(47): Show |
54 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.2173-432C>T | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190499583 | |||||||
| chr2:190499977 | T | C | 1 | a0001c0001t0003g0036 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2173-38T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190499977 | |||||||
| chr2:190499982 | G | A | 57 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(54): Show |
57 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.2173-33G>A | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190499982 | |||||||
| chr2:190500003 | T | C | 3 | a0003c0003t0010g0330 a0003c0003t0010g0331 a0003c0003t0022g0207 |
3 | HG03195.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2173-12T>C | MFSD6 | ENSG00000151690.15 | transcript | ENST00000392328.6 | protein_coding | 7/7 | chr2 | 190500003 |