Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84641 |
| ensemblid | ENSG00000148110.17 |
| hgncid | 23376 |
| symbol | MFSD14B |
| name | major facilitator superfamily domain containing 14B |
| refseq_nuc | NM_032558.3 |
| refseq_prot | NP_115947.2 |
| ensembl_nuc | ENST00000375344.8 |
| ensembl_prot | ENSP00000364493.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 94374569 |
| end | 94461042 |
| strand | + |
| ver | v1.2 |
| region | chr9:94374569-94461042 |
| region5000 | chr9:94369569-94466042 |
| regionname0 | MFSD14B_chr9_94374569_94461042 |
| regionname5000 | MFSD14B_chr9_94369569_94466042 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 506 | 349 | 78 | 69 | 144 | 16 | 40 | 106 | MFSD14B_chr9_94369569_94466042 | MFSD14B | MSVEP others(501): Show |
chr9 | 94369569 | 94466042 |
| a0002 | 0/0 | 506 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | MSVEP others(501): Show |
chr9 | 94369569 | 94466042 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1518 | 340 | 77 | 66 | 144 | 15 | 36 | MFSD14B_chr9_94369569_94466042 | MFSD14B | ATGAG others(1513): Show |
chr9 | 94369569 | 94466042 | ||
| a0001c0002 | 0/0 | 1518 | 8 | 0 | 3 | 0 | 1 | 4 | MFSD14B_chr9_94369569_94466042 | MFSD14B | ATGAG others(1513): Show |
chr9 | 94369569 | 94466042 | ||
| a0001c0003 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | ATGAG others(1513): Show |
chr9 | 94369569 | 94466042 | ||
| a0002c0004 | 0/0 | 1518 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | ATGAG others(1513): Show |
chr9 | 94369569 | 94466042 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3400 | 110 | 15 | 29 | 49 | 4 | 13 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3395): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0002 | 0/0 | 3401 | 75 | 28 | 6 | 36 | 4 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3396): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0003 | 1/0 | 3402 | 64 | 3 | 12 | 33 | 5 | 10 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3397): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0004 | 0/0 | 3401 | 35 | 5 | 6 | 16 | 0 | 8 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3396): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0005 | 0/0 | 3397 | 13 | 8 | 5 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3392): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0006 | 0/0 | 3400 | 11 | 7 | 2 | 1 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3395): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0007 | 0/0 | 3400 | 10 | 9 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3395): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0009 | 0/1 | 3402 | 4 | 0 | 2 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3397): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0010 | 0/0 | 3401 | 3 | 0 | 1 | 1 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3396): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0011 | 0/0 | 3402 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3397): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0012 | 0/0 | 3399 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3394): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0013 | 0/0 | 3399 | 2 | 0 | 0 | 1 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3394): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0014 | 0/0 | 3389 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3384): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0015 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3395): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0016 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3394): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0017 | 0/0 | 3401 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3396): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0018 | 0/0 | 3400 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3395): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0019 | 0/0 | 3401 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3396): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0021 | 0/0 | 3402 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3397): Show |
chr9 | 94369569 | 94466042 |
| a0001c0001t0022 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3395): Show |
chr9 | 94369569 | 94466042 |
| a0001c0002t0008 | 0/0 | 3400 | 7 | 0 | 3 | 0 | 1 | 3 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3395): Show |
chr9 | 94369569 | 94466042 |
| a0001c0002t0020 | 0/0 | 3401 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3396): Show |
chr9 | 94369569 | 94466042 |
| a0001c0003t0004 | 0/0 | 3401 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3396): Show |
chr9 | 94369569 | 94466042 |
| a0002c0004t0001 | 0/0 | 3400 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | GGTAA others(3395): Show |
chr9 | 94369569 | 94466042 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0009g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0009g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0009g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0009g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0010g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0010g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0011g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0012g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0012g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0013g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0013g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0014g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0016g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0017g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0018g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0019g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0021g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0022g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0008g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0008g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0008g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0008g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0008g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0008g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0008g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0020g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0003t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0002c0004t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | GBR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0206 | EUR | GBR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00140 | hp2 | a0001 | c0002 | t0008 | g0242 | EUR | GBR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0163 | EUR | FIN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00323 | hp2 | a0001 | c0001 | t0013 | g0331 | EUR | FIN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0254 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0026 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00741 | hp2 | a0001 | c0002 | t0008 | g0243 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01070 | hp1 | a0001 | c0001 | t0010 | g0150 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0015 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01255 | hp1 | a0001 | c0001 | t0019 | g0137 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01255 | hp2 | a0001 | c0002 | t0008 | g0240 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0141 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01257 | hp1 | a0001 | c0001 | t0009 | g0055 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01361 | hp1 | a0001 | c0002 | t0008 | g0244 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01361 | hp2 | a0001 | c0001 | t0018 | g0085 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0143 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0162 | EUR | IBS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | IBS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01517 | hp2 | a0001 | c0001 | t0010 | g0151 | EUR | IBS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02040 | hp2 | a0001 | c0001 | t0012 | g0024 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02132 | hp2 | a0001 | c0001 | t0012 | g0023 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02135 | hp2 | a0001 | c0001 | t0022 | g0287 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0065 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | CDX | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | CDX | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02293 | hp2 | a0002 | c0004 | t0001 | g0330 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02602 | hp1 | a0001 | c0002 | t0020 | g0246 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0025 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0108 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02647 | hp2 | a0001 | c0001 | t0016 | g0022 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02683 | hp1 | a0001 | c0001 | t0014 | g0006 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0046 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02698 | hp1 | a0001 | c0002 | t0008 | g0241 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02735 | hp1 | a0001 | c0001 | t0009 | g0050 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0251 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0071 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03139 | hp1 | a0001 | c0003 | t0004 | g0070 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03239 | hp1 | a0001 | c0002 | t0008 | g0239 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0053 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0072 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03704 | hp2 | a0001 | c0001 | t0017 | g0041 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0105 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0201 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0339 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0198 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04204 | hp2 | a0001 | c0002 | t0008 | g0245 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0064 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | CHB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | CHB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | YRI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | YRI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18966 | hp1 | a0001 | c0001 | t0021 | g0231 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18969 | hp2 | a0001 | c0001 | t0010 | g0188 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18970 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18992 | hp2 | a0001 | c0001 | t0013 | g0258 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19004 | hp2 | a0001 | c0001 | t0011 | g0197 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | LWK | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | LWK | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19058 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | YRI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | YRI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0208 | EUR | TSI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0144 | EUR | TSI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0142 | EUR | TSI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | GIH | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0056 | SAS | GIH | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | LWK | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0344 | AFR | LWK | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0062 | REF | REF | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0078 | REF | REF | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:94429217 | C | G | 1 | a0002 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.233C>G | p.Thr78Arg | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/12 | 484/3402 | 233/1521 | 78/506 | chr9 | 94429217 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:94446849 | T | C | 1 | a0001c0003 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.756T>C | p.Ser252Ser | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/12 | 1007/3402 | 756/1521 | 252/506 | chr9 | 94446849 | |||
| chr9:94459181 | G | A | 1 | a0001c0002 | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
synonymous_variant | LOW | c.1290G>A | p.Pro430Pro | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1541/3402 | 1290/1521 | 430/506 | chr9 | 94459181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:94374580 | G | C | 1 | a0001c0001t0014 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-240G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | 240 | chr9 | 94374580 | ||||||
| chr9:94374585 | G | C | 1 | a0001c0001t0015 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-235G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | 235 | chr9 | 94374585 | ||||||
| chr9:94374602 | A | C | 1 | a0001c0001t0014 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-218A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | 218 | chr9 | 94374602 | ||||||
| chr9:94374606 | G | C | 1 | a0001c0001t0016 | 1 | HG02647.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-214G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | chr9 | 94374606 | |||||||
| chr9:94374680 | CGGCGCCG others(5): Show |
C | 1 | a0001c0001t0014 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-128_-117delTGGCGC others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | 117 | INFO_REALIGN_3_PRIME | chr9 | 94374680 | |||||
| chr9:94374796 | G | A | 1 | a0001c0001t0014 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-24G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | 24 | chr9 | 94374796 | ||||||
| chr9:94459443 | C | T | 1 | a0001c0001t0022 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*31C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 31 | chr9 | 94459443 | ||||||
| chr9:94459572 | GT | G | 13 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(10): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*172delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 172 | INFO_REALIGN_3_PRIME | chr9 | 94459572 | |||||
| chr9:94459572 | GTT | G | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(3): Show |
55 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*171_*172delTT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 171 | INFO_REALIGN_3_PRIME | chr9 | 94459572 | |||||
| chr9:94459595 | C | CT | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(2): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*194dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 195 | INFO_REALIGN_3_PRIME | chr9 | 94459595 | |||||
| chr9:94459673 | G | A | 1 | a0001c0001t0016 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*261G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 261 | chr9 | 94459673 | ||||||
| chr9:94459674 | G | T | 1 | a0001c0001t0021 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*262G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 262 | chr9 | 94459674 | ||||||
| chr9:94459765 | G | A | 2 | a0001c0002t0008 a0001c0002t0020 |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*353G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 353 | chr9 | 94459765 | ||||||
| chr9:94460351 | A | G | 1 | a0001c0001t0011 | 3 | NA18970.hp1 NA19004.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*939A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 939 | chr9 | 94460351 | ||||||
| chr9:94460461 | A | C | 1 | a0001c0001t0017 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1049A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1049 | chr9 | 94460461 | ||||||
| chr9:94460497 | C | CTGAG | 4 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 others(1): Show |
40 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1087_*1090dupGAGT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1091 | INFO_REALIGN_3_PRIME | chr9 | 94460497 | |||||
| chr9:94460507 | C | T | 1 | a0001c0001t0007 | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1095C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1095 | chr9 | 94460507 | ||||||
| chr9:94460539 | T | C | 1 | a0001c0001t0018 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1127T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1127 | chr9 | 94460539 | ||||||
| chr9:94460606 | GGC | G | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(2): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1195_*1196delGC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1195 | chr9 | 94460606 | ||||||
| chr9:94460609 | C | T | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(2): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1197C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1197 | chr9 | 94460609 | ||||||
| chr9:94460610 | C | G | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(2): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1198C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1198 | chr9 | 94460610 | ||||||
| chr9:94460682 | AT | A | 4 | a0001c0001t0006 a0001c0001t0010 a0001c0002t0008 others(1): Show |
22 | HG00140.hp2 HG00544.hp1 HG00741.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1282delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1282 | INFO_REALIGN_3_PRIME | chr9 | 94460682 | |||||
| chr9:94460682 | ATT | A | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(11): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*1281_*1282delTT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1281 | INFO_REALIGN_3_PRIME | chr9 | 94460682 | |||||
| chr9:94460683 | T | A | 1 | a0001c0001t0002 | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1271T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1271 | chr9 | 94460683 | ||||||
| chr9:94460847 | A | G | 1 | a0001c0001t0019 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1435A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1435 | chr9 | 94460847 | ||||||
| chr9:94460931 | C | CT | 8 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(5): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1527dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1528 | INFO_REALIGN_3_PRIME | chr9 | 94460931 | |||||
| chr9:94461012 | C | G | 8 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(5): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1600C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1600 | chr9 | 94461012 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:94374951 | C | T | 1 | a0001c0001t0007g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.108+24C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94374951 | |||||||
| chr9:94374952 | T | G | 1 | a0001c0001t0014g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+25T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94374952 | |||||||
| chr9:94374961 | C | G | 1 | a0001c0001t0014g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+34C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94374961 | |||||||
| chr9:94374963 | C | A | 2 | a0001c0001t0003g0007 a0001c0001t0003g0008 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.108+36C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94374963 | |||||||
| chr9:94375051 | G | T | 33 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(30): Show |
33 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.108+124G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375051 | |||||||
| chr9:94375108 | G | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.108+181G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375108 | |||||||
| chr9:94375248 | A | C | 159 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(156): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.108+321A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375248 | |||||||
| chr9:94375263 | CAGGT | C | 11 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(8): Show |
11 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.108+340_108+343del others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94375263 | ||||||
| chr9:94375412 | A | G | 159 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(156): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.108+485A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375412 | |||||||
| chr9:94375467 | C | G | 1 | a0001c0001t0014g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+540C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375467 | |||||||
| chr9:94375486 | G | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(316): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.108+559G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375486 | |||||||
| chr9:94375553 | G | T | 1 | a0001c0001t0001g0343 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.108+626G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375553 | |||||||
| chr9:94375563 | A | G | 1 | a0001c0001t0014g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+636A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375563 | |||||||
| chr9:94375569 | C | G | 1 | a0001c0001t0014g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+642C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375569 | |||||||
| chr9:94375622 | A | AT | 57 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0002g0029 others(54): Show |
58 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+707dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94375622 | ||||||
| chr9:94375657 | A | G | 1 | a0001c0001t0014g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+730A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375657 | |||||||
| chr9:94375666 | C | G | 1 | a0001c0001t0003g0253 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.108+739C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375666 | |||||||
| chr9:94375733 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.108+806A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375733 | |||||||
| chr9:94375955 | C | T | 1 | a0001c0001t0003g0251 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.108+1028C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375955 | |||||||
| chr9:94375983 | A | G | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.108+1056A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375983 | |||||||
| chr9:94376194 | G | T | 1 | a0001c0001t0005g0077 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.108+1267G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376194 | |||||||
| chr9:94376452 | G | A | 1 | a0001c0001t0009g0026 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.108+1525G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376452 | |||||||
| chr9:94376738 | T | C | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+1811T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376738 | |||||||
| chr9:94376760 | C | G | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+1833C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376760 | |||||||
| chr9:94376848 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.108+1921C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376848 | |||||||
| chr9:94376879 | C | T | 338 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0083 others(335): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.108+1952C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376879 | |||||||
| chr9:94376880 | G | A | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+1953G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376880 | |||||||
| chr9:94376945 | G | T | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+2018G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376945 | |||||||
| chr9:94376946 | A | T | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+2019A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376946 | |||||||
| chr9:94377090 | A | T | 1 | a0001c0001t0003g0238 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.108+2163A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377090 | |||||||
| chr9:94377267 | T | G | 29 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(26): Show |
29 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.108+2340T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377267 | |||||||
| chr9:94377384 | GT | G | 119 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(116): Show |
120 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.108+2468delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377384 | ||||||
| chr9:94377385 | T | G | 1 | a0001c0001t0002g0170 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.108+2458T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377385 | |||||||
| chr9:94377498 | T | G | 4 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(1): Show |
4 | HG02818.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+2571T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377498 | |||||||
| chr9:94377530 | T | A | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+2603T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377530 | |||||||
| chr9:94377533 | C | CT | 31 | a0001c0001t0002g0109 a0001c0001t0002g0120 a0001c0001t0002g0121 others(28): Show |
31 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.108+2626dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377533 | ||||||
| chr9:94377533 | C | CTT | 14 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0112 others(11): Show |
14 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.108+2625_108+2626d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377533 | ||||||
| chr9:94377533 | CT | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0084 others(114): Show |
120 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.108+2626delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377533 | ||||||
| chr9:94377533 | CTT | C | 57 | a0001c0001t0001g0083 a0001c0001t0001g0256 a0001c0001t0002g0029 others(54): Show |
58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+2625_108+2626d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377533 | ||||||
| chr9:94377553 | T | A | 57 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(54): Show |
58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+2626T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377553 | |||||||
| chr9:94377553 | T | TA | 22 | a0001c0001t0002g0148 a0001c0001t0002g0248 a0001c0001t0002g0249 others(19): Show |
22 | HG00140.hp2 HG00544.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.108+2628dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377553 | ||||||
| chr9:94377553 | T | TTA | 85 | a0001c0001t0002g0004 a0001c0001t0002g0152 a0001c0001t0002g0157 others(82): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.108+2626_108+2627i others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377553 | |||||||
| chr9:94377553 | T | TTTA | 6 | a0001c0001t0002g0255 a0001c0001t0003g0232 a0001c0001t0003g0233 others(3): Show |
6 | HG01934.hp2 HG02055.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+2626_108+2627i others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377553 | |||||||
| chr9:94377724 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.108+2797C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377724 | |||||||
| chr9:94377808 | A | G | 2 | a0001c0001t0004g0073 a0001c0001t0004g0074 |
2 | HG00597.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.108+2881A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377808 | |||||||
| chr9:94377836 | G | A | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+2909G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377836 | |||||||
| chr9:94378018 | C | T | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+3091C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378018 | |||||||
| chr9:94378063 | CACTGCAC others(16): Show |
C | 11 | a0001c0001t0001g0082 a0001c0001t0007g0009 a0001c0001t0007g0010 others(8): Show |
11 | HG01081.hp1 HG01358.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.108+3161_108+3183d others(25): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94378063 | ||||||
| chr9:94378082 | G | A | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+3155G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378082 | |||||||
| chr9:94378113 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.108+3186G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378113 | |||||||
| chr9:94378126 | C | CA | 161 | a0001c0001t0001g0257 a0001c0001t0002g0004 a0001c0001t0002g0109 others(158): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.108+3212dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94378126 | ||||||
| chr9:94378260 | T | C | 216 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(213): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.108+3333T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378260 | |||||||
| chr9:94378387 | C | A | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+3460C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378387 | |||||||
| chr9:94378501 | A | G | 215 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(212): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.108+3574A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378501 | |||||||
| chr9:94378501 | A | T | 2 | a0001c0001t0003g0230 a0001c0001t0003g0235 |
2 | NA18983.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.108+3574A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378501 | |||||||
| chr9:94378559 | C | T | 3 | a0001c0001t0003g0142 a0001c0001t0006g0141 a0001c0001t0006g0143 |
3 | HG01256.hp2 HG01496.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.108+3632C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378559 | |||||||
| chr9:94378684 | C | G | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+3757C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378684 | |||||||
| chr9:94378792 | T | C | 1 | a0001c0001t0004g0027 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.108+3865T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378792 | |||||||
| chr9:94378937 | G | A | 1 | a0001c0001t0013g0258 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.108+4010G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378937 | |||||||
| chr9:94379052 | C | T | 1 | a0001c0001t0003g0229 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.108+4125C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379052 | |||||||
| chr9:94379089 | C | CTTTTTTT others(4): Show |
6 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0003g0153 others(3): Show |
6 | HG02273.hp2 HG02486.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+4166_108+4176d others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | ||||||
| chr9:94379089 | C | CTTTTTTT others(5): Show |
76 | a0001c0001t0002g0004 a0001c0001t0002g0157 a0001c0001t0002g0159 others(73): Show |
78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.108+4165_108+4176d others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | ||||||
| chr9:94379089 | C | CTTTTTTT others(6): Show |
30 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(27): Show |
30 | HG00597.hp2 HG00673.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.108+4164_108+4176d others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | ||||||
| chr9:94379089 | C | CTTTTTTT others(7): Show |
7 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0228 others(4): Show |
7 | HG02109.hp1 HG02135.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+4163_108+4176d others(16): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | ||||||
| chr9:94379089 | C | CTTTTTTT others(10): Show |
7 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(4): Show |
7 | HG00544.hp1 HG01884.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+4176_108+4177i others(19): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | ||||||
| chr9:94379089 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0006g0107 a0001c0001t0006g0108 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.108+4176_108+4177i others(20): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | ||||||
| chr9:94379089 | CTTTT | C | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.108+4173_108+4176d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | ||||||
| chr9:94379133 | C | T | 1 | a0001c0001t0003g0213 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.108+4206C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379133 | |||||||
| chr9:94379138 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.108+4211G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379138 | |||||||
| chr9:94379179 | C | T | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+4252C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379179 | |||||||
| chr9:94379180 | G | A | 1 | a0001c0001t0014g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+4253G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379180 | |||||||
| chr9:94379248 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.108+4321G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379248 | |||||||
| chr9:94379297 | G | A | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+4370G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379297 | |||||||
| chr9:94379323 | C | T | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+4396C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379323 | |||||||
| chr9:94379386 | C | CT | 14 | a0001c0001t0001g0082 a0001c0001t0003g0226 a0001c0001t0003g0238 others(11): Show |
14 | HG00544.hp1 HG01358.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.108+4476dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379386 | ||||||
| chr9:94379386 | CT | C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(19): Show |
23 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.108+4476delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379386 | ||||||
| chr9:94379422 | CTG | C | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+4497_108+4498d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379422 | ||||||
| chr9:94379442 | C | T | 1 | a0001c0001t0013g0258 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.108+4515C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379442 | |||||||
| chr9:94379443 | G | A | 216 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(213): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.108+4516G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379443 | |||||||
| chr9:94379843 | A | G | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.108+4916A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379843 | |||||||
| chr9:94379868 | C | T | 4 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(1): Show |
4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+4941C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379868 | |||||||
| chr9:94379935 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.108+5008G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379935 | |||||||
| chr9:94379962 | G | C | 1 | a0001c0001t0012g0023 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.108+5035G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379962 | |||||||
| chr9:94379984 | T | G | 2 | a0001c0001t0007g0009 a0001c0001t0007g0010 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.108+5057T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379984 | |||||||
| chr9:94380184 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.108+5257G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94380184 | |||||||
| chr9:94380463 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.108+5536G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94380463 | |||||||
| chr9:94380551 | G | A | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+5624G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94380551 | |||||||
| chr9:94380618 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.108+5691C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94380618 | |||||||
| chr9:94380696 | C | A | 1 | a0001c0001t0001g0262 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.108+5769C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94380696 | |||||||
| chr9:94380855 | G | GTA | 216 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(213): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.108+5929_108+5930i others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94380855 | ||||||
| chr9:94381040 | C | CT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(85): Show |
90 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.108+6126dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94381040 | ||||||
| chr9:94381040 | CT | C | 155 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(152): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.108+6126delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94381040 | ||||||
| chr9:94381248 | C | A | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+6321C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381248 | |||||||
| chr9:94381263 | C | T | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+6336C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381263 | |||||||
| chr9:94381352 | C | CT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0338 a0001c0001t0001g0340 others(3): Show |
8 | NA18944.hp2 NA18950.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.108+6439dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94381352 | ||||||
| chr9:94381361 | T | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.108+6434T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381361 | |||||||
| chr9:94381364 | T | G | 58 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(55): Show |
59 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.108+6437T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381364 | |||||||
| chr9:94381446 | T | TA | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.108+6520dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94381446 | ||||||
| chr9:94381459 | A | G | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+6532A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381459 | |||||||
| chr9:94381525 | T | C | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.108+6598T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381525 | |||||||
| chr9:94381615 | A | G | 2 | a0001c0001t0002g0210 a0001c0001t0003g0209 |
2 | HG00408.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.108+6688A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381615 | |||||||
| chr9:94381622 | T | A | 7 | a0001c0001t0005g0002 a0001c0001t0005g0030 a0001c0001t0005g0031 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+6695T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381622 | |||||||
| chr9:94381701 | T | C | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+6774T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381701 | |||||||
| chr9:94381902 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.108+6975T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381902 | |||||||
| chr9:94382037 | T | C | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+7110T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382037 | |||||||
| chr9:94382043 | T | C | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.108+7116T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382043 | |||||||
| chr9:94382045 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0335 a0001c0001t0001g0336 others(1): Show |
4 | HG00733.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+7118C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382045 | |||||||
| chr9:94382167 | C | T | 1 | a0001c0003t0004g0070 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108+7240C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382167 | |||||||
| chr9:94382172 | A | G | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+7245A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382172 | |||||||
| chr9:94382302 | C | G | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(1): Show |
4 | HG00140.hp1 HG01074.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+7375C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382302 | |||||||
| chr9:94382333 | A | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(303): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.108+7406A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382333 | |||||||
| chr9:94382363 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.108+7436C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382363 | |||||||
| chr9:94382390 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.108+7463A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382390 | |||||||
| chr9:94382471 | T | C | 1 | a0001c0001t0003g0158 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.108+7544T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382471 | |||||||
| chr9:94382718 | G | A | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+7791G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382718 | |||||||
| chr9:94382897 | G | A | 1 | a0001c0001t0004g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.108+7970G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382897 | |||||||
| chr9:94382906 | G | A | 10 | a0001c0001t0001g0257 a0001c0001t0001g0263 a0001c0001t0001g0264 others(7): Show |
10 | HG01069.hp2 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.108+7979G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382906 | |||||||
| chr9:94383096 | T | C | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+8169T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383096 | |||||||
| chr9:94383161 | C | CT | 58 | a0001c0001t0001g0257 a0001c0001t0001g0271 a0001c0001t0002g0029 others(55): Show |
59 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.108+8253dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94383161 | ||||||
| chr9:94383161 | C | CTT | 43 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(40): Show |
43 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.108+8252_108+8253d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94383161 | ||||||
| chr9:94383161 | C | CTTT | 112 | a0001c0001t0002g0004 a0001c0001t0002g0120 a0001c0001t0002g0121 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.108+8251_108+8253d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94383161 | ||||||
| chr9:94383161 | C | CTTTT | 6 | a0001c0001t0002g0140 a0001c0001t0002g0224 a0001c0001t0003g0203 others(3): Show |
6 | HG02027.hp2 HG02074.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+8250_108+8253d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94383161 | ||||||
| chr9:94383277 | C | T | 2 | a0001c0001t0003g0007 a0001c0001t0003g0008 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.108+8350C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383277 | |||||||
| chr9:94383370 | C | T | 1 | a0001c0001t0004g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108+8443C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383370 | |||||||
| chr9:94383451 | A | G | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+8524A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383451 | |||||||
| chr9:94383496 | A | G | 1 | a0001c0001t0001g0334 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.108+8569A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383496 | |||||||
| chr9:94383643 | A | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.108+8716A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383643 | |||||||
| chr9:94383754 | A | C | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+8827A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383754 | |||||||
| chr9:94383929 | A | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0034 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.108+9002A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383929 | |||||||
| chr9:94384133 | C | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+9206C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384133 | |||||||
| chr9:94384182 | A | G | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+9255A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384182 | |||||||
| chr9:94384336 | C | CT | 66 | a0001c0001t0001g0340 a0001c0001t0002g0183 a0001c0001t0002g0210 others(63): Show |
67 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.108+9426dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94384336 | ||||||
| chr9:94384478 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0272 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.108+9551T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384478 | |||||||
| chr9:94384581 | A | G | 1 | a0001c0001t0014g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+9654A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384581 | |||||||
| chr9:94384615 | C | G | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.108+9688C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384615 | |||||||
| chr9:94384620 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.108+9693A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384620 | |||||||
| chr9:94384670 | C | T | 1 | a0001c0001t0007g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+9743C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384670 | |||||||
| chr9:94384700 | C | A | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+9773C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384700 | |||||||
| chr9:94384744 | A | C | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.108+9817A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384744 | |||||||
| chr9:94384786 | G | T | 1 | a0001c0001t0007g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.108+9859G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384786 | |||||||
| chr9:94384933 | A | G | 1 | a0001c0001t0003g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.108+10006A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384933 | |||||||
| chr9:94384981 | C | G | 1 | a0001c0001t0003g0202 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.108+10054C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384981 | |||||||
| chr9:94385375 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.108+10448G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385375 | |||||||
| chr9:94385548 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.108+10621A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385548 | |||||||
| chr9:94385558 | G | A | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+10631G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385558 | |||||||
| chr9:94385569 | G | A | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+10642G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385569 | |||||||
| chr9:94385716 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.108+10789C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385716 | |||||||
| chr9:94385750 | G | A | 217 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(214): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.108+10823G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385750 | |||||||
| chr9:94385859 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108+10932C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385859 | |||||||
| chr9:94386246 | T | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.108+11319T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386246 | |||||||
| chr9:94386266 | T | A | 1 | a0001c0001t0002g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.108+11339T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386266 | |||||||
| chr9:94386267 | C | CAT | 249 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.108+11340_108+1134 others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386267 | |||||||
| chr9:94386407 | G | A | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+11480G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386407 | |||||||
| chr9:94386481 | G | GT | 4 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(1): Show |
4 | HG00741.hp1 NA18944.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+11556dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94386481 | ||||||
| chr9:94386536 | A | G | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+11609A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386536 | |||||||
| chr9:94386564 | C | G | 159 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(156): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.108+11637C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386564 | |||||||
| chr9:94386652 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.108+11725A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386652 | |||||||
| chr9:94387032 | A | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+12105A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387032 | |||||||
| chr9:94387066 | C | T | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.108+12139C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387066 | |||||||
| chr9:94387080 | T | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.108+12153T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387080 | |||||||
| chr9:94387081 | C | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0228 |
2 | NA18967.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.108+12154C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387081 | |||||||
| chr9:94387151 | A | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+12224A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387151 | |||||||
| chr9:94387281 | G | C | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+12354G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387281 | |||||||
| chr9:94387427 | A | AT | 57 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(54): Show |
58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+12510dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94387427 | ||||||
| chr9:94387427 | AT | A | 14 | a0001c0001t0002g0152 a0001c0001t0003g0162 a0001c0001t0003g0182 others(11): Show |
14 | HG01081.hp1 HG01192.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.108+12510delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94387427 | ||||||
| chr9:94387628 | G | C | 14 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(11): Show |
14 | HG00423.hp1 HG03239.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.108+12701G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387628 | |||||||
| chr9:94387880 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.108+12953G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387880 | |||||||
| chr9:94387923 | T | C | 4 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(1): Show |
4 | HG02818.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+12996T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387923 | |||||||
| chr9:94388066 | A | G | 36 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0042 others(33): Show |
36 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.108+13139A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388066 | |||||||
| chr9:94388122 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0036 |
2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.108+13195G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388122 | |||||||
| chr9:94388141 | A | AG | 217 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(214): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.108+13214_108+1321 others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388141 | |||||||
| chr9:94388206 | GAAAAAAG others(6): Show |
G | 4 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 others(1): Show |
4 | HG02698.hp2 HG02738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+13284_108+1329 others(17): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94388206 | ||||||
| chr9:94388321 | A | T | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+13394A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388321 | |||||||
| chr9:94388340 | T | G | 49 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.108+13413T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388340 | |||||||
| chr9:94388373 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.108+13446G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388373 | |||||||
| chr9:94388804 | A | G | 3 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 |
3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.108+13877A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388804 | |||||||
| chr9:94388912 | C | T | 217 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(214): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.108+13985C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388912 | |||||||
| chr9:94388961 | C | T | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+14034C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388961 | |||||||
| chr9:94388974 | A | C | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 |
3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.108+14047A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388974 | |||||||
| chr9:94389059 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.108+14132G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389059 | |||||||
| chr9:94389134 | ATAGT | A | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 |
3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.108+14211_108+1421 others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94389134 | ||||||
| chr9:94389203 | A | G | 1 | a0001c0001t0003g0251 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.108+14276A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389203 | |||||||
| chr9:94389271 | G | GT | 66 | a0001c0001t0001g0332 a0001c0001t0002g0029 a0001c0001t0002g0036 others(63): Show |
67 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.108+14356dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94389271 | ||||||
| chr9:94389450 | A | T | 53 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(50): Show |
54 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.108+14523A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389450 | |||||||
| chr9:94389452 | T | A | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+14525T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389452 | |||||||
| chr9:94389525 | C | T | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.108+14598C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389525 | |||||||
| chr9:94389526 | G | A | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+14599G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389526 | |||||||
| chr9:94389669 | C | T | 1 | a0002c0004t0001g0330 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.108+14742C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389669 | |||||||
| chr9:94389714 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.108+14787C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389714 | |||||||
| chr9:94389791 | A | G | 1 | a0001c0001t0004g0069 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.108+14864A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389791 | |||||||
| chr9:94389799 | G | T | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+14872G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389799 | |||||||
| chr9:94389923 | A | G | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+14996A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389923 | |||||||
| chr9:94390028 | C | T | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+15101C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390028 | |||||||
| chr9:94390082 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.108+15155C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390082 | |||||||
| chr9:94390093 | A | G | 1 | a0001c0001t0001g0332 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.108+15166A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390093 | |||||||
| chr9:94390103 | A | G | 49 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.108+15176A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390103 | |||||||
| chr9:94390123 | A | G | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+15196A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390123 | |||||||
| chr9:94390136 | C | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+15209C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390136 | |||||||
| chr9:94390169 | G | A | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+15242G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390169 | |||||||
| chr9:94390171 | G | C | 1 | a0001c0001t0001g0273 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.108+15244G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390171 | |||||||
| chr9:94390180 | T | C | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+15253T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390180 | |||||||
| chr9:94390275 | A | G | 217 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(214): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.108+15348A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390275 | |||||||
| chr9:94390322 | T | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+15395T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390322 | |||||||
| chr9:94390350 | G | A | 217 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(214): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.108+15423G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390350 | |||||||
| chr9:94390371 | G | C | 1 | a0001c0001t0002g0004 | 2 | HG02083.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.108+15444G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390371 | |||||||
| chr9:94390505 | C | T | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+15578C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390505 | |||||||
| chr9:94390515 | ACAGTCC | A | 4 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 others(1): Show |
4 | HG02698.hp2 HG02738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+15589_108+1559 others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390515 | |||||||
| chr9:94390525 | C | T | 1 | a0001c0001t0007g0011 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.108+15598C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390525 | |||||||
| chr9:94390553 | G | T | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+15626G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390553 | |||||||
| chr9:94390628 | A | G | 2 | a0001c0001t0007g0009 a0001c0001t0007g0010 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.108+15701A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390628 | |||||||
| chr9:94390804 | A | T | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+15877A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390804 | |||||||
| chr9:94390843 | G | A | 1 | a0001c0001t0017g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.108+15916G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390843 | |||||||
| chr9:94391076 | G | A | 1 | a0001c0001t0003g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.108+16149G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391076 | |||||||
| chr9:94391197 | C | CA | 13 | a0001c0001t0002g0110 a0001c0001t0002g0121 a0001c0001t0002g0123 others(10): Show |
13 | HG00741.hp1 HG01243.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.108+16292dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94391197 | ||||||
| chr9:94391197 | CA | C | 14 | a0001c0001t0001g0256 a0001c0001t0001g0270 a0001c0001t0001g0329 others(11): Show |
14 | HG01069.hp2 HG01255.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.108+16292delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94391197 | ||||||
| chr9:94391234 | C | T | 5 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.108+16307C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391234 | |||||||
| chr9:94391323 | A | G | 1 | a0001c0001t0004g0067 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.108+16396A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391323 | |||||||
| chr9:94391362 | TA | T | 9 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(6): Show |
9 | HG02040.hp2 HG02132.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.108+16450delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94391362 | ||||||
| chr9:94391377 | A | C | 1 | a0001c0001t0006g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.108+16450A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391377 | |||||||
| chr9:94391413 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.108+16486G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391413 | |||||||
| chr9:94391590 | C | T | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.108+16663C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391590 | |||||||
| chr9:94391651 | G | T | 1 | a0001c0001t0004g0045 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.108+16724G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391651 | |||||||
| chr9:94391652 | T | C | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+16725T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391652 | |||||||
| chr9:94391714 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.108+16787T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391714 | |||||||
| chr9:94391741 | C | T | 340 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0081 others(337): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.108+16814C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391741 | |||||||
| chr9:94391748 | G | A | 2 | a0001c0001t0006g0102 a0001c0001t0006g0107 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.108+16821G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391748 | |||||||
| chr9:94391847 | C | G | 7 | a0001c0001t0001g0273 a0001c0001t0001g0281 a0001c0001t0001g0282 others(4): Show |
7 | HG00423.hp1 NA18953.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+16920C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391847 | |||||||
| chr9:94391888 | T | A | 59 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(56): Show |
59 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.108+16961T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391888 | |||||||
| chr9:94392009 | C | T | 3 | a0001c0001t0003g0222 a0001c0001t0003g0223 a0001c0001t0003g0227 |
3 | HG00597.hp2 HG00673.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.108+17082C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392009 | |||||||
| chr9:94392025 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.108+17098C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392025 | |||||||
| chr9:94392125 | G | C | 7 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(4): Show |
7 | HG01884.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+17198G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392125 | |||||||
| chr9:94392244 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.108+17317T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392244 | |||||||
| chr9:94392444 | G | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(303): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.108+17517G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392444 | |||||||
| chr9:94392469 | G | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+17542G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392469 | |||||||
| chr9:94392506 | AT | A | 160 | a0001c0001t0001g0288 a0001c0001t0002g0004 a0001c0001t0002g0109 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+17592delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94392506 | ||||||
| chr9:94392586 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108+17659C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392586 | |||||||
| chr9:94392619 | G | A | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.108+17692G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392619 | |||||||
| chr9:94392756 | C | T | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.108+17829C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392756 | |||||||
| chr9:94392794 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.108+17867C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392794 | |||||||
| chr9:94392830 | GATC | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.108+17907_108+1790 others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94392830 | ||||||
| chr9:94392843 | A | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+17916A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392843 | |||||||
| chr9:94392971 | A | T | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.108+18044A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392971 | |||||||
| chr9:94393068 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.108+18141G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393068 | |||||||
| chr9:94393353 | G | C | 1 | a0001c0001t0002g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.108+18426G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393353 | |||||||
| chr9:94393442 | G | A | 2 | a0001c0001t0004g0035 a0001c0001t0004g0037 |
2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.108+18515G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393442 | |||||||
| chr9:94393452 | A | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+18525A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393452 | |||||||
| chr9:94393550 | T | C | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+18623T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393550 | |||||||
| chr9:94393658 | G | C | 10 | a0001c0001t0001g0259 a0001c0001t0001g0262 a0001c0001t0001g0289 others(7): Show |
10 | HG00621.hp1 HG01261.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.108+18731G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393658 | |||||||
| chr9:94393823 | G | A | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+18896G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393823 | |||||||
| chr9:94393860 | G | A | 5 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0015 others(2): Show |
5 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.108+18933G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393860 | |||||||
| chr9:94393911 | A | ATCCTGTT others(2): Show |
217 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(214): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.108+18986_108+1898 others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94393911 | ||||||
| chr9:94393995 | T | A | 1 | a0001c0001t0007g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.108+19068T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393995 | |||||||
| chr9:94394060 | T | A | 1 | a0001c0001t0003g0227 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.108+19133T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394060 | |||||||
| chr9:94394199 | G | C | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+19272G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394199 | |||||||
| chr9:94394337 | T | A | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+19410T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394337 | |||||||
| chr9:94394450 | AT | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(114): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.108+19537delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94394450 | ||||||
| chr9:94394595 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0272 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.108+19668G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394595 | |||||||
| chr9:94394636 | T | C | 1 | a0001c0001t0005g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.108+19709T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394636 | |||||||
| chr9:94394787 | T | A | 1 | a0001c0001t0001g0296 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.108+19860T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394787 | |||||||
| chr9:94394840 | T | C | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+19913T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394840 | |||||||
| chr9:94394887 | C | T | 1 | a0001c0001t0003g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.108+19960C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394887 | |||||||
| chr9:94394914 | T | G | 1 | a0001c0001t0002g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.108+19987T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394914 | |||||||
| chr9:94394915 | G | GT | 59 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(56): Show |
59 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.108+20004dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94394915 | ||||||
| chr9:94394915 | G | GTT | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.108+20003_108+2000 others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94394915 | ||||||
| chr9:94394915 | G | T | 1 | a0001c0001t0002g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.108+19988G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394915 | |||||||
| chr9:94394918 | T | TG | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+19991_108+1999 others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394918 | |||||||
| chr9:94394922 | T | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(85): Show |
90 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.108+19995T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394922 | |||||||
| chr9:94394953 | G | A | 2 | a0001c0001t0006g0105 a0001c0001t0006g0254 |
2 | HG00544.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.108+20026G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394953 | |||||||
| chr9:94395005 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0019g0137 |
2 | HG01255.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.108+20078C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395005 | |||||||
| chr9:94395059 | G | A | 5 | a0001c0001t0001g0261 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG00438.hp2 HG00673.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-20099G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395059 | |||||||
| chr9:94395068 | C | T | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-20090C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395068 | |||||||
| chr9:94395149 | A | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-20009A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395149 | |||||||
| chr9:94395189 | C | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-19969C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395189 | |||||||
| chr9:94395232 | A | G | 10 | a0001c0001t0001g0261 a0001c0001t0001g0297 a0001c0001t0001g0298 others(7): Show |
10 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.109-19926A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395232 | |||||||
| chr9:94395270 | A | G | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.109-19888A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395270 | |||||||
| chr9:94395290 | T | C | 19 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0126 others(16): Show |
19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.109-19868T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395290 | |||||||
| chr9:94395306 | T | C | 2 | a0001c0001t0002g0136 a0001c0001t0019g0137 |
2 | HG01255.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.109-19852T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395306 | |||||||
| chr9:94395443 | GC | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-19714delC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395443 | |||||||
| chr9:94395545 | G | T | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-19613G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395545 | |||||||
| chr9:94395722 | A | G | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-19436A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395722 | |||||||
| chr9:94395945 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.109-19213G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395945 | |||||||
| chr9:94396005 | T | C | 1 | a0001c0001t0003g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.109-19153T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396005 | |||||||
| chr9:94396141 | GATA | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-19012_109-1901 others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94396141 | ||||||
| chr9:94396203 | G | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(303): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.109-18955G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396203 | |||||||
| chr9:94396447 | G | A | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-18711G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396447 | |||||||
| chr9:94396492 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.109-18666G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396492 | |||||||
| chr9:94396517 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.109-18641C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396517 | |||||||
| chr9:94396563 | A | G | 1 | a0001c0001t0007g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109-18595A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396563 | |||||||
| chr9:94396596 | G | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(316): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.109-18562G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396596 | |||||||
| chr9:94396683 | C | T | 217 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(214): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.109-18475C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396683 | |||||||
| chr9:94396705 | T | C | 1 | a0001c0001t0001g0300 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.109-18453T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396705 | |||||||
| chr9:94396758 | C | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-18400C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396758 | |||||||
| chr9:94396801 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.109-18357G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396801 | |||||||
| chr9:94396957 | A | T | 1 | a0001c0002t0008g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.109-18201A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396957 | |||||||
| chr9:94397001 | C | T | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-18157C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397001 | |||||||
| chr9:94397144 | C | T | 65 | a0001c0001t0002g0183 a0001c0001t0002g0210 a0001c0001t0003g0149 others(62): Show |
66 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.109-18014C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397144 | |||||||
| chr9:94397354 | T | C | 1 | a0001c0001t0003g0235 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.109-17804T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397354 | |||||||
| chr9:94397404 | T | C | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-17754T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397404 | |||||||
| chr9:94397487 | GA | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0083 others(276): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.109-17660delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94397487 | ||||||
| chr9:94397501 | A | G | 3 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 |
3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.109-17657A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397501 | |||||||
| chr9:94397666 | C | T | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-17492C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397666 | |||||||
| chr9:94397693 | G | A | 4 | a0001c0001t0007g0014 a0001c0001t0007g0015 a0001c0001t0007g0016 others(1): Show |
4 | HG01081.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-17465G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397693 | |||||||
| chr9:94397700 | G | C | 217 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(214): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.109-17458G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397700 | |||||||
| chr9:94397756 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.109-17402G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397756 | |||||||
| chr9:94397869 | C | G | 2 | a0001c0001t0003g0234 a0001c0001t0004g0069 |
2 | HG02602.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.109-17289C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397869 | |||||||
| chr9:94397901 | G | T | 1 | a0001c0001t0004g0069 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.109-17257G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397901 | |||||||
| chr9:94398008 | C | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.109-17150C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398008 | |||||||
| chr9:94398043 | A | G | 217 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(214): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.109-17115A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398043 | |||||||
| chr9:94398070 | G | C | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-17088G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398070 | |||||||
| chr9:94398170 | A | G | 60 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(57): Show |
60 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.109-16988A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398170 | |||||||
| chr9:94398224 | G | GT | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-16925dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94398224 | ||||||
| chr9:94398233 | T | A | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-16925T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398233 | |||||||
| chr9:94398354 | G | T | 7 | a0001c0001t0005g0002 a0001c0001t0005g0030 a0001c0001t0005g0031 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-16804G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398354 | |||||||
| chr9:94398561 | A | G | 1 | a0001c0001t0007g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.109-16597A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398561 | |||||||
| chr9:94398591 | C | T | 1 | a0001c0001t0004g0076 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.109-16567C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398591 | |||||||
| chr9:94398831 | T | G | 57 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(54): Show |
58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-16327T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398831 | |||||||
| chr9:94398899 | C | T | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-16259C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398899 | |||||||
| chr9:94399042 | C | T | 4 | a0001c0001t0007g0014 a0001c0001t0007g0015 a0001c0001t0007g0016 others(1): Show |
4 | HG01081.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-16116C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399042 | |||||||
| chr9:94399047 | T | A | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-16111T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399047 | |||||||
| chr9:94399058 | C | T | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-16100C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399058 | |||||||
| chr9:94399116 | C | T | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-16042C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399116 | |||||||
| chr9:94399147 | C | G | 1 | a0001c0001t0001g0286 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.109-16011C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399147 | |||||||
| chr9:94399183 | C | T | 3 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0107 |
3 | HG02922.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.109-15975C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399183 | |||||||
| chr9:94399254 | A | G | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-15904A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399254 | |||||||
| chr9:94399301 | G | C | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-15857G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399301 | |||||||
| chr9:94399363 | C | T | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-15795C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399363 | |||||||
| chr9:94399399 | T | C | 4 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-15759T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399399 | |||||||
| chr9:94399428 | G | A | 1 | a0001c0001t0003g0154 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.109-15730G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399428 | |||||||
| chr9:94399538 | A | T | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-15620A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399538 | |||||||
| chr9:94399608 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.109-15550A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399608 | |||||||
| chr9:94399730 | C | T | 4 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(1): Show |
4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-15428C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399730 | |||||||
| chr9:94399784 | G | T | 216 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(213): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.109-15374G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399784 | |||||||
| chr9:94399807 | C | CT | 37 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(34): Show |
39 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.109-15336dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94399807 | ||||||
| chr9:94399807 | CT | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0083 others(181): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.109-15336delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94399807 | ||||||
| chr9:94399823 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.109-15335G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399823 | |||||||
| chr9:94399835 | C | T | 1 | a0001c0001t0004g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109-15323C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399835 | |||||||
| chr9:94399868 | C | T | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.109-15290C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399868 | |||||||
| chr9:94399906 | T | G | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-15252T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399906 | |||||||
| chr9:94399963 | G | A | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-15195G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399963 | |||||||
| chr9:94399975 | A | G | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-15183A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399975 | |||||||
| chr9:94400038 | T | C | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-15120T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400038 | |||||||
| chr9:94400055 | C | T | 8 | a0001c0001t0003g0156 a0001c0001t0003g0164 a0001c0001t0003g0165 others(5): Show |
8 | HG01070.hp1 HG01123.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-15103C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400055 | |||||||
| chr9:94400060 | C | G | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-15098C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400060 | |||||||
| chr9:94400171 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.109-14987C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400171 | |||||||
| chr9:94400186 | G | A | 1 | a0001c0001t0003g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.109-14972G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400186 | |||||||
| chr9:94400208 | TATGTACC others(10): Show |
T | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 |
3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.109-14944_109-1492 others(21): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94400208 | ||||||
| chr9:94400228 | G | T | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-14930G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400228 | |||||||
| chr9:94400234 | A | G | 1 | a0001c0001t0003g0155 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.109-14924A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400234 | |||||||
| chr9:94400496 | T | G | 45 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(42): Show |
45 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.109-14662T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400496 | |||||||
| chr9:94400509 | G | GA | 166 | a0001c0001t0001g0100 a0001c0001t0002g0004 a0001c0001t0002g0029 others(163): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.109-14637dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94400509 | ||||||
| chr9:94400544 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.109-14614A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400544 | |||||||
| chr9:94400567 | T | C | 2 | a0001c0001t0007g0009 a0001c0001t0007g0010 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.109-14591T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400567 | |||||||
| chr9:94400568 | G | GA | 197 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(194): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.109-14577dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94400568 | ||||||
| chr9:94400568 | G | GAAAAA | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-14581_109-1457 others(9): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94400568 | ||||||
| chr9:94400702 | G | A | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-14456G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400702 | |||||||
| chr9:94400848 | A | C | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-14310A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400848 | |||||||
| chr9:94400959 | C | CTT | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-14197_109-1419 others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94400959 | ||||||
| chr9:94401088 | C | CT | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-14058dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94401088 | ||||||
| chr9:94401088 | CT | C | 7 | a0001c0001t0004g0047 a0001c0001t0004g0048 a0001c0001t0004g0049 others(4): Show |
7 | NA18995.hp2 NA19000.hp2 NA19001.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-14058delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94401088 | ||||||
| chr9:94401151 | A | G | 1 | a0001c0001t0002g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.109-14007A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401151 | |||||||
| chr9:94401193 | C | T | 1 | a0001c0001t0007g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109-13965C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401193 | |||||||
| chr9:94401194 | G | A | 1 | a0001c0001t0001g0288 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.109-13964G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401194 | |||||||
| chr9:94401202 | A | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-13956A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401202 | |||||||
| chr9:94401305 | G | T | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-13853G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401305 | |||||||
| chr9:94401506 | T | A | 5 | a0001c0001t0005g0002 a0001c0001t0005g0030 a0001c0001t0005g0031 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-13652T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401506 | |||||||
| chr9:94401601 | G | C | 4 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(1): Show |
4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-13557G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401601 | |||||||
| chr9:94401639 | G | C | 3 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 |
3 | HG01081.hp1 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.109-13519G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401639 | |||||||
| chr9:94401650 | G | C | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-13508G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401650 | |||||||
| chr9:94401876 | G | A | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.109-13282G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401876 | |||||||
| chr9:94401915 | A | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-13243A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401915 | |||||||
| chr9:94401973 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.109-13185C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401973 | |||||||
| chr9:94401994 | G | A | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.109-13164G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401994 | |||||||
| chr9:94402032 | G | A | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-13126G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402032 | |||||||
| chr9:94402126 | C | A | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-13032C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402126 | |||||||
| chr9:94402198 | G | A | 1 | a0001c0001t0006g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.109-12960G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402198 | |||||||
| chr9:94402254 | G | A | 97 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-12904G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402254 | |||||||
| chr9:94402300 | A | G | 7 | a0001c0001t0005g0002 a0001c0001t0005g0030 a0001c0001t0005g0031 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-12858A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402300 | |||||||
| chr9:94402401 | G | GT | 49 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.109-12750dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94402401 | ||||||
| chr9:94402408 | T | A | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-12750T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402408 | |||||||
| chr9:94402826 | A | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-12332A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402826 | |||||||
| chr9:94402966 | A | G | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-12192A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402966 | |||||||
| chr9:94403263 | A | C | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-11895A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403263 | |||||||
| chr9:94403282 | G | A | 5 | a0001c0001t0005g0002 a0001c0001t0005g0030 a0001c0001t0005g0031 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-11876G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403282 | |||||||
| chr9:94403415 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.109-11743G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403415 | |||||||
| chr9:94403416 | G | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-11742G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403416 | |||||||
| chr9:94403503 | C | CT | 37 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(34): Show |
37 | HG00140.hp1 HG00639.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.109-11642dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94403503 | ||||||
| chr9:94403503 | CT | C | 8 | a0001c0001t0001g0289 a0001c0001t0001g0322 a0001c0001t0002g0167 others(5): Show |
8 | HG02165.hp1 HG02735.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-11642delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94403503 | ||||||
| chr9:94403535 | A | G | 2 | a0001c0001t0003g0207 a0001c0001t0003g0208 |
2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.109-11623A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403535 | |||||||
| chr9:94403552 | T | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.109-11606T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403552 | |||||||
| chr9:94403585 | G | C | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-11573G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403585 | |||||||
| chr9:94404127 | A | G | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(1): Show |
4 | HG00140.hp1 HG01074.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-11031A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404127 | |||||||
| chr9:94404347 | A | G | 42 | a0001c0001t0001g0269 a0001c0001t0001g0318 a0001c0001t0002g0029 others(39): Show |
42 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.109-10811A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404347 | |||||||
| chr9:94404381 | C | T | 157 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(154): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.109-10777C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404381 | |||||||
| chr9:94404405 | T | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(20): Show |
24 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.109-10753T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404405 | |||||||
| chr9:94404525 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.109-10633A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404525 | |||||||
| chr9:94404563 | T | G | 1 | a0001c0001t0001g0297 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.109-10595T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404563 | |||||||
| chr9:94404567 | A | G | 2 | a0001c0001t0006g0105 a0001c0001t0006g0254 |
2 | HG00544.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.109-10591A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404567 | |||||||
| chr9:94404636 | G | A | 5 | a0001c0001t0005g0002 a0001c0001t0005g0030 a0001c0001t0005g0031 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-10522G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404636 | |||||||
| chr9:94404646 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.109-10512T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404646 | |||||||
| chr9:94404677 | TTTAA | T | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-10478_109-1047 others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94404677 | ||||||
| chr9:94405044 | A | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-10114A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405044 | |||||||
| chr9:94405217 | C | T | 7 | a0001c0001t0005g0002 a0001c0001t0005g0030 a0001c0001t0005g0031 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-9941C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405217 | |||||||
| chr9:94405240 | A | G | 1 | a0001c0001t0002g0175 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.109-9918A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405240 | |||||||
| chr9:94405267 | G | A | 3 | a0001c0001t0004g0051 a0001c0001t0004g0073 a0001c0001t0004g0074 |
3 | HG00597.hp1 NA19009.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.109-9891G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405267 | |||||||
| chr9:94405291 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.109-9867C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405291 | |||||||
| chr9:94405315 | G | GA | 7 | a0001c0001t0005g0002 a0001c0001t0005g0030 a0001c0001t0005g0031 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-9840dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94405315 | ||||||
| chr9:94405446 | C | T | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG03239.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.109-9712C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405446 | |||||||
| chr9:94405474 | G | C | 1 | a0001c0001t0001g0322 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.109-9684G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405474 | |||||||
| chr9:94405485 | C | T | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-9673C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405485 | |||||||
| chr9:94405493 | C | T | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0014g0006 |
3 | HG00639.hp1 HG01109.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.109-9665C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405493 | |||||||
| chr9:94405498 | C | CA | 49 | a0001c0001t0001g0086 a0001c0001t0001g0274 a0001c0001t0001g0301 others(46): Show |
49 | HG00639.hp1 HG00639.hp2 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.109-9640dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94405498 | ||||||
| chr9:94405498 | C | CAA | 6 | a0001c0001t0002g0124 a0001c0001t0002g0126 a0001c0001t0002g0128 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-9641_109-9640d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94405498 | ||||||
| chr9:94405498 | CA | C | 6 | a0001c0001t0001g0097 a0001c0001t0001g0278 a0001c0001t0003g0165 others(3): Show |
6 | HG00323.hp2 HG01167.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-9640delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94405498 | ||||||
| chr9:94405596 | T | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-9562T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405596 | |||||||
| chr9:94405640 | T | TTATTCTG others(9): Show |
1 | a0001c0001t0003g0177 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.109-9517_109-9502d others(18): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94405640 | ||||||
| chr9:94405737 | A | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-9421A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405737 | |||||||
| chr9:94406014 | C | G | 60 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(57): Show |
60 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.109-9144C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406014 | |||||||
| chr9:94406066 | A | AT | 9 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG00323.hp1 HG01358.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-9071dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | ||||||
| chr9:94406066 | A | ATT | 7 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0007g0010 others(4): Show |
7 | HG01975.hp1 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-9072_109-9071d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | ||||||
| chr9:94406066 | A | ATTT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0086 others(20): Show |
24 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.109-9073_109-9071d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | ||||||
| chr9:94406066 | A | ATTTT | 58 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0259 others(55): Show |
59 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.109-9074_109-9071d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | ||||||
| chr9:94406066 | A | ATTTTT | 167 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(164): Show |
171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.109-9075_109-9071d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | ||||||
| chr9:94406066 | A | ATTTTTT | 57 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0276 others(54): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-9076_109-9071d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | ||||||
| chr9:94406066 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0002g0248 a0001c0001t0002g0250 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-9081_109-9071d others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | ||||||
| chr9:94406066 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0002g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.109-9082_109-9071d others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | ||||||
| chr9:94406066 | AT | A | 7 | a0001c0001t0001g0299 a0001c0001t0001g0303 a0001c0001t0001g0304 others(4): Show |
7 | HG02165.hp2 HG02293.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-9071delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | ||||||
| chr9:94406156 | C | T | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-9002C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406156 | |||||||
| chr9:94406249 | A | AT | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-8907dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406249 | ||||||
| chr9:94406252 | A | T | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-8906A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406252 | |||||||
| chr9:94406365 | A | G | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.109-8793A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406365 | |||||||
| chr9:94406573 | A | G | 1 | a0001c0001t0006g0141 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.109-8585A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406573 | |||||||
| chr9:94406585 | A | G | 1 | a0001c0001t0004g0063 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.109-8573A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406585 | |||||||
| chr9:94406637 | C | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-8521C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406637 | |||||||
| chr9:94406907 | G | A | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | NA18998.hp2 NA19011.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.109-8251G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406907 | |||||||
| chr9:94406910 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.109-8248T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406910 | |||||||
| chr9:94407130 | GT | G | 52 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.109-8027delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407130 | |||||||
| chr9:94407211 | T | G | 1 | a0001c0001t0005g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.109-7947T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407211 | |||||||
| chr9:94407216 | T | C | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-7942T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407216 | |||||||
| chr9:94407381 | CT | C | 11 | a0001c0001t0001g0322 a0001c0001t0001g0340 a0001c0001t0002g0139 others(8): Show |
11 | HG02165.hp1 HG02451.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.109-7762delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94407381 | ||||||
| chr9:94407453 | A | T | 1 | a0001c0001t0002g0161 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.109-7705A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407453 | |||||||
| chr9:94407479 | A | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-7679A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407479 | |||||||
| chr9:94407535 | C | T | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.109-7623C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407535 | |||||||
| chr9:94407585 | G | T | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-7573G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407585 | |||||||
| chr9:94407626 | C | G | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-7532C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407626 | |||||||
| chr9:94407762 | G | A | 1 | a0001c0001t0005g0018 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.109-7396G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407762 | |||||||
| chr9:94407813 | A | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-7345A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407813 | |||||||
| chr9:94407836 | T | C | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-7322T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407836 | |||||||
| chr9:94408100 | A | G | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-7058A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408100 | |||||||
| chr9:94408140 | A | C | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-7018A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408140 | |||||||
| chr9:94408174 | T | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0318 |
2 | HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.109-6984T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408174 | |||||||
| chr9:94408222 | C | A | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-6936C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408222 | |||||||
| chr9:94408311 | C | G | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | NA18998.hp2 NA19011.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.109-6847C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408311 | |||||||
| chr9:94408504 | G | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-6654G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408504 | |||||||
| chr9:94408582 | G | A | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-6576G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408582 | |||||||
| chr9:94408665 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.109-6493A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408665 | |||||||
| chr9:94408825 | TTG | T | 28 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(25): Show |
28 | HG00140.hp2 HG00544.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.109-6331_109-6330d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94408825 | ||||||
| chr9:94408826 | TG | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(102): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.109-6331delG | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408826 | |||||||
| chr9:94408827 | G | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0256 others(188): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.109-6331G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408827 | |||||||
| chr9:94408829 | T | G | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-6329T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408829 | |||||||
| chr9:94408831 | G | GTTT | 6 | a0001c0001t0001g0259 a0001c0001t0001g0289 a0001c0001t0001g0293 others(3): Show |
6 | HG00621.hp1 HG01261.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-6326_109-6324d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94408831 | ||||||
| chr9:94408831 | G | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(89): Show |
93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.109-6327G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408831 | |||||||
| chr9:94408834 | T | G | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-6324T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408834 | |||||||
| chr9:94408835 | G | T | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-6323G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408835 | |||||||
| chr9:94408875 | T | C | 4 | a0001c0001t0007g0014 a0001c0001t0007g0015 a0001c0001t0007g0016 others(1): Show |
4 | HG01081.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-6283T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408875 | |||||||
| chr9:94408975 | C | T | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-6183C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408975 | |||||||
| chr9:94408992 | A | G | 1 | a0001c0001t0007g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.109-6166A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408992 | |||||||
| chr9:94409055 | G | A | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-6103G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409055 | |||||||
| chr9:94409129 | C | CT | 60 | a0001c0001t0002g0004 a0001c0001t0002g0110 a0001c0001t0002g0112 others(57): Show |
62 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.109-6002dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | C | CTT | 13 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0299 others(10): Show |
13 | HG01256.hp1 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.109-6003_109-6002d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | C | CTTT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(56): Show |
61 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.109-6004_109-6002d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | C | CTTTT | 20 | a0001c0001t0001g0268 a0001c0001t0001g0271 a0001c0001t0001g0277 others(17): Show |
20 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.109-6005_109-6002d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | C | CTTTTTT | 7 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-6007_109-6002d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | C | CTTTTTTT | 9 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0093 others(6): Show |
9 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-6008_109-6002d others(9): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0007g0011 a0001c0001t0007g0015 |
2 | HG01081.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.109-6011_109-6002d others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | C | CTTTTTTT others(4): Show |
5 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0013 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-6012_109-6002d others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0007g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.109-6014_109-6002d others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0007g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109-6017_109-6002d others(18): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | CT | C | 71 | a0001c0001t0002g0029 a0001c0001t0002g0039 a0001c0001t0002g0040 others(68): Show |
71 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.109-6002delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-6012_109-6002d others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409129 | CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0004g0047 a0001c0001t0004g0048 a0001c0001t0004g0049 others(4): Show |
7 | NA18995.hp2 NA19000.hp2 NA19001.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-6014_109-6002d others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | ||||||
| chr9:94409266 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0096 |
2 | HG02300.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.109-5892A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409266 | |||||||
| chr9:94409366 | GTCTTAAC others(1): Show |
G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(244): Show |
251 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.109-5783_109-5776d others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409366 | ||||||
| chr9:94409599 | A | G | 1 | a0001c0001t0005g0032 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.109-5559A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409599 | |||||||
| chr9:94409681 | T | G | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.109-5477T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409681 | |||||||
| chr9:94409703 | G | T | 1 | a0001c0001t0004g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.109-5455G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409703 | |||||||
| chr9:94409898 | G | GTT | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.109-5259_109-5258d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409898 | ||||||
| chr9:94409943 | T | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.109-5215T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409943 | |||||||
| chr9:94410247 | C | T | 1 | a0001c0001t0003g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.109-4911C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410247 | |||||||
| chr9:94410350 | A | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-4808A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410350 | |||||||
| chr9:94410404 | AT | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(177): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.109-4747delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94410404 | ||||||
| chr9:94410417 | C | T | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-4741C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410417 | |||||||
| chr9:94410458 | T | TG | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-4699dupG | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94410458 | ||||||
| chr9:94410506 | G | A | 2 | a0001c0001t0004g0028 a0001c0001t0004g0067 |
2 | HG00639.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.109-4652G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410506 | |||||||
| chr9:94410519 | C | T | 1 | a0001c0001t0003g0158 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.109-4639C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410519 | |||||||
| chr9:94410664 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.109-4494C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410664 | |||||||
| chr9:94410750 | C | G | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-4408C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410750 | |||||||
| chr9:94410922 | C | T | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-4236C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410922 | |||||||
| chr9:94411067 | T | C | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-4091T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411067 | |||||||
| chr9:94411170 | T | C | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-3988T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411170 | |||||||
| chr9:94411585 | G | A | 2 | a0001c0001t0007g0009 a0001c0001t0007g0010 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.109-3573G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411585 | |||||||
| chr9:94411593 | A | AT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(25): Show |
29 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.109-3551dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94411593 | ||||||
| chr9:94411593 | AT | A | 15 | a0001c0001t0001g0303 a0001c0001t0002g0109 a0001c0001t0002g0110 others(12): Show |
15 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.109-3551delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94411593 | ||||||
| chr9:94411651 | C | G | 1 | a0001c0001t0003g0177 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.109-3507C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411651 | |||||||
| chr9:94411652 | G | C | 1 | a0001c0001t0003g0177 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.109-3506G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411652 | |||||||
| chr9:94411719 | T | A | 1 | a0001c0001t0002g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.109-3439T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411719 | |||||||
| chr9:94411877 | C | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-3281C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411877 | |||||||
| chr9:94411933 | A | G | 1 | a0001c0001t0006g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.109-3225A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411933 | |||||||
| chr9:94412318 | G | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-2840G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94412318 | |||||||
| chr9:94412568 | C | A | 2 | a0001c0001t0001g0333 a0002c0004t0001g0330 |
2 | HG02293.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.109-2590C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94412568 | |||||||
| chr9:94412619 | G | A | 2 | a0001c0001t0004g0027 a0001c0001t0004g0052 |
2 | NA19079.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.109-2539G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94412619 | |||||||
| chr9:94412791 | A | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-2367A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94412791 | |||||||
| chr9:94412890 | T | A | 1 | a0001c0001t0006g0106 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-2268T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94412890 | |||||||
| chr9:94413006 | T | A | 1 | a0001c0001t0001g0328 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.109-2152T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413006 | |||||||
| chr9:94413007 | A | T | 25 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(22): Show |
25 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.109-2151A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413007 | |||||||
| chr9:94413008 | A | T | 1 | a0001c0001t0001g0276 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.109-2150A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413008 | |||||||
| chr9:94413013 | T | A | 30 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(27): Show |
30 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.109-2145T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413013 | |||||||
| chr9:94413101 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.109-2057A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413101 | |||||||
| chr9:94413192 | A | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-1966A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413192 | |||||||
| chr9:94413492 | G | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.109-1666G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413492 | |||||||
| chr9:94413605 | A | ATCCCAG | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-1553_109-1552i others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413605 | |||||||
| chr9:94413659 | C | CA | 101 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0111 others(98): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.109-1481dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94413659 | ||||||
| chr9:94413659 | C | CAA | 18 | a0001c0001t0002g0224 a0001c0001t0002g0228 a0001c0001t0004g0060 others(15): Show |
18 | HG00140.hp2 HG00741.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.109-1482_109-1481d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94413659 | ||||||
| chr9:94413659 | C | CAAA | 49 | a0001c0001t0001g0294 a0001c0001t0001g0299 a0001c0001t0002g0029 others(46): Show |
49 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.109-1483_109-1481d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94413659 | ||||||
| chr9:94413659 | C | CAAAA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0079 a0001c0001t0001g0080 others(99): Show |
105 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.109-1484_109-1481d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94413659 | ||||||
| chr9:94413659 | C | CAAAAA | 24 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(21): Show |
25 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.109-1485_109-1481d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94413659 | ||||||
| chr9:94413719 | A | G | 1 | a0001c0001t0006g0254 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.109-1439A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413719 | |||||||
| chr9:94413810 | T | A | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.109-1348T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413810 | |||||||
| chr9:94413818 | C | T | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-1340C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413818 | |||||||
| chr9:94413865 | A | G | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-1293A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413865 | |||||||
| chr9:94413943 | G | T | 1 | a0001c0001t0002g0171 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.109-1215G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413943 | |||||||
| chr9:94414086 | T | C | 2 | a0001c0001t0011g0005 a0001c0001t0011g0197 |
3 | NA18970.hp1 NA19004.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.109-1072T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414086 | |||||||
| chr9:94414443 | G | A | 1 | a0001c0001t0004g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.109-715G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414443 | |||||||
| chr9:94414446 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(123): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.109-712C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414446 | |||||||
| chr9:94414683 | A | G | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.109-475A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414683 | |||||||
| chr9:94414686 | G | A | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.109-472G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414686 | |||||||
| chr9:94414728 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.109-430C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414728 | |||||||
| chr9:94414786 | A | G | 19 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0126 others(16): Show |
19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.109-372A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414786 | |||||||
| chr9:94414831 | A | G | 42 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(39): Show |
42 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.109-327A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414831 | |||||||
| chr9:94414948 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.109-210A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414948 | |||||||
| chr9:94414950 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(241): Show |
248 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.109-208A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414950 | |||||||
| chr9:94414952 | C | T | 1 | a0001c0001t0003g0203 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.109-206C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414952 | |||||||
| chr9:94414956 | C | G | 1 | a0001c0001t0001g0302 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.109-202C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414956 | |||||||
| chr9:94414966 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.109-192G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414966 | |||||||
| chr9:94414978 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.109-180C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414978 | |||||||
| chr9:94415020 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.109-138G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94415020 | |||||||
| chr9:94415321 | G | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+68G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415321 | |||||||
| chr9:94415359 | A | G | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.204+106A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415359 | |||||||
| chr9:94415385 | G | GT | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(176): Show |
183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.204+144dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94415385 | ||||||
| chr9:94415387 | T | G | 1 | a0001c0001t0002g0228 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.204+134T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415387 | |||||||
| chr9:94415471 | T | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.204+218T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415471 | |||||||
| chr9:94415544 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.204+291C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415544 | |||||||
| chr9:94415571 | A | G | 6 | a0001c0001t0002g0122 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01255.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+318A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415571 | |||||||
| chr9:94415707 | A | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(188): Show |
195 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.204+454A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415707 | |||||||
| chr9:94416009 | C | T | 2 | a0001c0001t0005g0002 a0001c0001t0016g0022 |
3 | HG01069.hp1 HG01071.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.204+756C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416009 | |||||||
| chr9:94416020 | T | C | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.204+767T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416020 | |||||||
| chr9:94416061 | G | C | 1 | a0001c0001t0002g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.204+808G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416061 | |||||||
| chr9:94416081 | T | C | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+828T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416081 | |||||||
| chr9:94416086 | C | T | 11 | a0001c0001t0003g0212 a0001c0001t0007g0009 a0001c0001t0007g0010 others(8): Show |
11 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+833C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416086 | |||||||
| chr9:94416242 | C | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.204+989C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416242 | |||||||
| chr9:94416432 | C | T | 19 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(16): Show |
19 | HG00140.hp2 HG00741.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.204+1179C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416432 | |||||||
| chr9:94416466 | G | A | 1 | a0001c0001t0001g0284 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.204+1213G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416466 | |||||||
| chr9:94416507 | C | T | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.204+1254C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416507 | |||||||
| chr9:94416570 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(53): Show |
58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.204+1317T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416570 | |||||||
| chr9:94416673 | G | C | 1 | a0001c0001t0003g0177 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.204+1420G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416673 | |||||||
| chr9:94416784 | G | T | 1 | a0001c0001t0003g0185 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.204+1531G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416784 | |||||||
| chr9:94416791 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.204+1538T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416791 | |||||||
| chr9:94416827 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.204+1574T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416827 | |||||||
| chr9:94416854 | C | CA | 6 | a0001c0001t0002g0152 a0001c0001t0002g0216 a0001c0001t0002g0228 others(3): Show |
6 | HG00408.hp1 HG04204.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+1617dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94416854 | ||||||
| chr9:94416854 | CA | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(190): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.204+1617delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94416854 | ||||||
| chr9:94417106 | T | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+1853T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417106 | |||||||
| chr9:94417141 | A | G | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+1888A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417141 | |||||||
| chr9:94417344 | T | C | 46 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(43): Show |
46 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.204+2091T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417344 | |||||||
| chr9:94417354 | G | A | 1 | a0001c0001t0004g0061 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.204+2101G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417354 | |||||||
| chr9:94417433 | C | T | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 |
3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.204+2180C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417433 | |||||||
| chr9:94417456 | A | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.204+2203A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417456 | |||||||
| chr9:94417566 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.204+2313A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417566 | |||||||
| chr9:94417666 | T | C | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.204+2413T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417666 | |||||||
| chr9:94417688 | A | G | 1 | a0001c0001t0007g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.204+2435A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417688 | |||||||
| chr9:94417790 | T | C | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+2537T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417790 | |||||||
| chr9:94417808 | C | T | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+2555C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417808 | |||||||
| chr9:94417833 | C | A | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+2580C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417833 | |||||||
| chr9:94417849 | T | TCCCGCCC others(3): Show |
1 | a0001c0001t0002g0138 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.204+2599_204+2600i others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417849 | ||||||
| chr9:94417849 | TCCCACCC others(4): Show |
T | 7 | a0001c0001t0002g0124 a0001c0001t0002g0128 a0001c0001t0002g0129 others(4): Show |
7 | HG01256.hp2 HG02015.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+2600_204+2610d others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417849 | ||||||
| chr9:94417849 | TCCCACCC others(5): Show |
T | 1 | a0001c0001t0002g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.204+2600_204+2611d others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417849 | ||||||
| chr9:94417853 | A | C | 8 | a0001c0001t0002g0126 a0001c0001t0002g0131 a0001c0001t0002g0132 others(5): Show |
8 | HG01109.hp2 HG01496.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+2600A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417853 | |||||||
| chr9:94417853 | ACCCCACC others(3): Show |
A | 3 | a0001c0001t0002g0125 a0001c0001t0002g0135 a0001c0001t0019g0137 |
3 | HG01255.hp1 HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.204+2605_204+2614d others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417853 | ||||||
| chr9:94417858 | A | C | 18 | a0001c0001t0002g0121 a0001c0001t0002g0126 a0001c0001t0002g0127 others(15): Show |
18 | HG00639.hp1 HG01109.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.204+2605A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417858 | |||||||
| chr9:94417858 | AC | A | 23 | a0001c0001t0002g0179 a0001c0001t0002g0183 a0001c0001t0002g0210 others(20): Show |
23 | HG00408.hp1 HG00544.hp2 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.204+2623delC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417858 | ||||||
| chr9:94417858 | ACCCCCC | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0093 others(16): Show |
20 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+2618_204+2623d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417858 | ||||||
| chr9:94417858 | ACCCCCCC | A | 20 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0086 others(17): Show |
20 | HG00099.hp2 HG00733.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+2617_204+2623d others(9): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417858 | ||||||
| chr9:94417858 | ACCCCCCC others(1): Show |
A | 25 | a0001c0001t0001g0267 a0001c0001t0001g0288 a0001c0001t0001g0297 others(22): Show |
25 | HG00323.hp2 HG00673.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.204+2616_204+2623d others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417858 | ||||||
| chr9:94417858 | ACCCCCCC others(2): Show |
A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(129): Show |
135 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.204+2615_204+2623d others(11): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417858 | ||||||
| chr9:94417862 | C | A | 1 | a0001c0001t0002g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.204+2609C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417862 | |||||||
| chr9:94417864 | C | G | 3 | a0001c0001t0002g0183 a0001c0001t0003g0149 a0001c0001t0003g0202 |
3 | HG00544.hp2 NA18747.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.204+2611C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417864 | |||||||
| chr9:94417872 | C | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.204+2619C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417872 | |||||||
| chr9:94417874 | C | G | 10 | a0001c0001t0002g0210 a0001c0001t0003g0153 a0001c0001t0003g0190 others(7): Show |
10 | HG00408.hp1 HG00621.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.204+2621C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417874 | |||||||
| chr9:94417917 | C | T | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.204+2664C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417917 | |||||||
| chr9:94417920 | G | A | 1 | a0001c0001t0003g0235 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.204+2667G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417920 | |||||||
| chr9:94418002 | T | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.204+2749T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418002 | |||||||
| chr9:94418017 | C | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.204+2764C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418017 | |||||||
| chr9:94418048 | C | T | 5 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(2): Show |
5 | HG02818.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+2795C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418048 | |||||||
| chr9:94418049 | G | A | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.204+2796G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418049 | |||||||
| chr9:94418052 | A | G | 215 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(212): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.204+2799A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418052 | |||||||
| chr9:94418107 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(123): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.204+2854C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418107 | |||||||
| chr9:94418279 | T | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(53): Show |
58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.204+3026T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418279 | |||||||
| chr9:94418287 | G | T | 25 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(22): Show |
25 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.204+3034G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418287 | |||||||
| chr9:94418338 | T | G | 1 | a0001c0002t0020g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.204+3085T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418338 | |||||||
| chr9:94418361 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.204+3108A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418361 | |||||||
| chr9:94418395 | T | C | 45 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(42): Show |
45 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.204+3142T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418395 | |||||||
| chr9:94418424 | C | T | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.204+3171C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418424 | |||||||
| chr9:94418435 | G | A | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.204+3182G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418435 | |||||||
| chr9:94418443 | C | T | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+3190C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418443 | |||||||
| chr9:94418450 | T | G | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+3197T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418450 | |||||||
| chr9:94418537 | G | T | 1 | a0001c0001t0003g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.204+3284G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418537 | |||||||
| chr9:94418656 | G | A | 5 | a0001c0002t0008g0239 a0001c0002t0008g0241 a0001c0002t0008g0242 others(2): Show |
5 | HG00140.hp2 HG00741.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+3403G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418656 | |||||||
| chr9:94418687 | C | T | 1 | a0001c0001t0003g0213 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.204+3434C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418687 | |||||||
| chr9:94418713 | T | G | 1 | a0001c0001t0004g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.204+3460T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418713 | |||||||
| chr9:94418754 | A | T | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.204+3501A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418754 | |||||||
| chr9:94418757 | C | CT | 22 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(19): Show |
22 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.204+3522dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94418757 | ||||||
| chr9:94418757 | CT | C | 55 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(52): Show |
56 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.204+3522delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94418757 | ||||||
| chr9:94418772 | T | G | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.204+3519T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418772 | |||||||
| chr9:94418773 | T | C | 2 | a0001c0001t0002g0248 a0001c0001t0002g0250 |
2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.204+3520T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418773 | |||||||
| chr9:94418775 | T | TC | 3 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 |
3 | HG02818.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.204+3523dupC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94418775 | ||||||
| chr9:94418775 | T | TTC | 19 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.204+3522_204+3523i others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418775 | |||||||
| chr9:94418919 | C | T | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.204+3666C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418919 | |||||||
| chr9:94419115 | T | G | 3 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 |
3 | HG02818.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.204+3862T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419115 | |||||||
| chr9:94419172 | G | A | 25 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(22): Show |
25 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.204+3919G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419172 | |||||||
| chr9:94419275 | G | A | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.204+4022G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419275 | |||||||
| chr9:94419298 | C | CT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(120): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.204+4061dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94419298 | ||||||
| chr9:94419298 | CT | C | 62 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(59): Show |
63 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.204+4061delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94419298 | ||||||
| chr9:94419302 | T | TC | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+4049_204+4050i others(3): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419302 | |||||||
| chr9:94419369 | C | T | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+4116C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419369 | |||||||
| chr9:94419428 | G | C | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.204+4175G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419428 | |||||||
| chr9:94419442 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.204+4189C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419442 | |||||||
| chr9:94419464 | T | G | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.204+4211T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419464 | |||||||
| chr9:94419464 | T | TTTTTG | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+4223_204+4227d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94419464 | ||||||
| chr9:94419492 | T | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.204+4239T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419492 | |||||||
| chr9:94419512 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.204+4259A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419512 | |||||||
| chr9:94419547 | C | T | 1 | a0001c0001t0004g0059 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.204+4294C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419547 | |||||||
| chr9:94419549 | C | G | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.204+4296C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419549 | |||||||
| chr9:94419559 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.204+4306C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419559 | |||||||
| chr9:94419698 | C | A | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+4445C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419698 | |||||||
| chr9:94419756 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.204+4503T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419756 | |||||||
| chr9:94419980 | T | C | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+4727T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419980 | |||||||
| chr9:94420055 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.204+4802T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420055 | |||||||
| chr9:94420357 | G | C | 2 | a0001c0001t0006g0106 a0001c0001t0006g0108 |
2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.204+5104G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420357 | |||||||
| chr9:94420381 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.204+5128G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420381 | |||||||
| chr9:94420539 | G | T | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.204+5286G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420539 | |||||||
| chr9:94420595 | C | CT | 32 | a0001c0001t0001g0083 a0001c0001t0001g0290 a0001c0001t0001g0334 others(29): Show |
32 | HG00639.hp1 HG01255.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.204+5357dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94420595 | ||||||
| chr9:94420595 | CT | C | 8 | a0001c0001t0001g0270 a0001c0001t0002g0175 a0001c0001t0003g0158 others(5): Show |
8 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+5357delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94420595 | ||||||
| chr9:94420623 | A | T | 2 | a0001c0001t0003g0207 a0001c0001t0003g0208 |
2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.204+5370A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420623 | |||||||
| chr9:94420747 | A | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.204+5494A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420747 | |||||||
| chr9:94420823 | C | A | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+5570C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420823 | |||||||
| chr9:94420857 | C | A | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.204+5604C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420857 | |||||||
| chr9:94421071 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.204+5818T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421071 | |||||||
| chr9:94421116 | T | C | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+5863T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421116 | |||||||
| chr9:94421132 | G | GT | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.204+5880dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94421132 | ||||||
| chr9:94421392 | G | A | 1 | a0001c0002t0008g0240 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.204+6139G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421392 | |||||||
| chr9:94421430 | T | A | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+6177T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421430 | |||||||
| chr9:94421784 | G | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.204+6531G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421784 | |||||||
| chr9:94421880 | C | T | 5 | a0001c0001t0004g0035 a0001c0001t0004g0037 a0001c0001t0004g0038 others(2): Show |
5 | HG02896.hp1 HG02970.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+6627C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421880 | |||||||
| chr9:94421930 | C | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+6677C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421930 | |||||||
| chr9:94422114 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.204+6861C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422114 | |||||||
| chr9:94422399 | A | G | 2 | a0001c0001t0001g0312 a0001c0001t0001g0323 |
2 | HG00408.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.205-6790A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422399 | |||||||
| chr9:94422469 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.205-6720G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422469 | |||||||
| chr9:94422481 | G | C | 1 | a0001c0001t0002g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.205-6708G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422481 | |||||||
| chr9:94422520 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.205-6669G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422520 | |||||||
| chr9:94422545 | A | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.205-6644A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422545 | |||||||
| chr9:94422935 | C | CT | 32 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(29): Show |
33 | HG00099.hp1 HG00558.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.205-6239dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94422935 | ||||||
| chr9:94422935 | CT | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.205-6239delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94422935 | ||||||
| chr9:94422943 | T | C | 49 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.205-6246T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422943 | |||||||
| chr9:94422999 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.205-6190C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422999 | |||||||
| chr9:94423029 | C | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
2 | HG00099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.205-6160C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423029 | |||||||
| chr9:94423055 | G | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-6134G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423055 | |||||||
| chr9:94423265 | CT | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.205-5909delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94423265 | ||||||
| chr9:94423267 | T | C | 2 | a0001c0001t0007g0015 a0001c0001t0022g0287 |
2 | HG01081.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.205-5922T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423267 | |||||||
| chr9:94423268 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(120): Show |
126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.205-5921T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423268 | |||||||
| chr9:94423269 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.205-5920T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423269 | |||||||
| chr9:94423270 | T | C | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.205-5919T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423270 | |||||||
| chr9:94423290 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.205-5899C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423290 | |||||||
| chr9:94423330 | T | TG | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.205-5859_205-5858i others(3): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423330 | |||||||
| chr9:94423415 | G | T | 1 | a0001c0001t0003g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.205-5774G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423415 | |||||||
| chr9:94423445 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.205-5744G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423445 | |||||||
| chr9:94423670 | C | A | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.205-5519C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423670 | |||||||
| chr9:94423676 | T | A | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.205-5513T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423676 | |||||||
| chr9:94423942 | CT | C | 45 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(42): Show |
45 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.205-5242delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94423942 | ||||||
| chr9:94423971 | A | G | 4 | a0001c0001t0002g0159 a0001c0001t0002g0166 a0001c0001t0002g0218 others(1): Show |
4 | NA18951.hp1 NA18967.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-5218A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423971 | |||||||
| chr9:94424135 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.205-5054G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424135 | |||||||
| chr9:94424231 | T | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.205-4958T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424231 | |||||||
| chr9:94424242 | C | CG | 24 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(21): Show |
24 | HG00323.hp1 HG00544.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.205-4945dupG | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424242 | ||||||
| chr9:94424245 | A | C | 7 | a0001c0001t0005g0002 a0001c0001t0005g0030 a0001c0001t0005g0031 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-4944A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424245 | |||||||
| chr9:94424245 | A | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(144): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.205-4944A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424245 | |||||||
| chr9:94424245 | A | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.205-4944A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424245 | |||||||
| chr9:94424298 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.205-4891G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424298 | |||||||
| chr9:94424496 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(178): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.205-4693A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424496 | |||||||
| chr9:94424658 | G | C | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.205-4531G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424658 | |||||||
| chr9:94424664 | A | G | 1 | a0001c0001t0002g0123 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.205-4525A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424664 | |||||||
| chr9:94424709 | T | A | 4 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(1): Show |
4 | HG02818.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-4480T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424709 | |||||||
| chr9:94424717 | T | C | 11 | a0001c0001t0001g0308 a0001c0001t0007g0009 a0001c0001t0007g0010 others(8): Show |
11 | HG01081.hp1 HG01106.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.205-4472T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424717 | |||||||
| chr9:94424727 | C | CT | 53 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(50): Show |
53 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.205-4439dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424727 | ||||||
| chr9:94424727 | C | CTT | 15 | a0001c0001t0002g0138 a0001c0001t0002g0144 a0001c0001t0002g0248 others(12): Show |
15 | HG00544.hp1 HG00741.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.205-4440_205-4439d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424727 | ||||||
| chr9:94424727 | CT | C | 36 | a0001c0001t0002g0004 a0001c0001t0002g0148 a0001c0001t0002g0152 others(33): Show |
37 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.205-4439delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424727 | ||||||
| chr9:94424727 | CTTTTT | C | 56 | a0001c0001t0001g0260 a0001c0001t0001g0303 a0001c0001t0001g0341 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.205-4443_205-4439d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424727 | ||||||
| chr9:94424727 | CTTTTTT | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(118): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.205-4444_205-4439d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424727 | ||||||
| chr9:94424856 | C | T | 1 | a0001c0001t0004g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.205-4333C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424856 | |||||||
| chr9:94424857 | G | A | 1 | a0001c0001t0003g0187 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.205-4332G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424857 | |||||||
| chr9:94424915 | T | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(17): Show |
21 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.205-4274T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424915 | |||||||
| chr9:94424916 | T | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0083 others(56): Show |
62 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.205-4273T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424916 | |||||||
| chr9:94424917 | T | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0083 others(108): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.205-4272T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424917 | |||||||
| chr9:94424918 | T | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.205-4271T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424918 | |||||||
| chr9:94424918 | TA | T | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.205-4268delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424918 | ||||||
| chr9:94424919 | A | T | 10 | a0001c0001t0002g0119 a0001c0001t0002g0140 a0001c0002t0008g0239 others(7): Show |
10 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.205-4270A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424919 | |||||||
| chr9:94424932 | C | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.205-4257C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424932 | |||||||
| chr9:94425038 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.205-4151A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425038 | |||||||
| chr9:94425091 | G | C | 217 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0036 others(214): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.205-4098G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425091 | |||||||
| chr9:94425145 | A | C | 160 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(157): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.205-4044A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425145 | |||||||
| chr9:94425182 | T | C | 1 | a0001c0001t0002g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.205-4007T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425182 | |||||||
| chr9:94425204 | T | G | 2 | a0001c0001t0007g0009 a0001c0001t0007g0010 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.205-3985T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425204 | |||||||
| chr9:94425231 | G | C | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.205-3958G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425231 | |||||||
| chr9:94425253 | G | A | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.205-3936G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425253 | |||||||
| chr9:94425380 | C | T | 7 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0133 others(4): Show |
7 | HG02015.hp1 HG03834.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-3809C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425380 | |||||||
| chr9:94425723 | TA | T | 3 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0107 |
3 | HG02922.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.205-3464delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94425723 | ||||||
| chr9:94426077 | C | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.205-3112C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94426077 | |||||||
| chr9:94426208 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.205-2981G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94426208 | |||||||
| chr9:94426268 | A | G | 1 | a0001c0001t0007g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.205-2921A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94426268 | |||||||
| chr9:94426587 | G | T | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.205-2602G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94426587 | |||||||
| chr9:94426738 | A | AT | 8 | a0001c0001t0001g0300 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
8 | HG00408.hp2 HG00438.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-2444dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94426738 | ||||||
| chr9:94426757 | CATTTT | C | 52 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.205-2424_205-2420d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94426757 | ||||||
| chr9:94427190 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.205-1999T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427190 | |||||||
| chr9:94427582 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.205-1607T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427582 | |||||||
| chr9:94427619 | C | T | 1 | a0001c0001t0004g0063 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.205-1570C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427619 | |||||||
| chr9:94427662 | G | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-1527G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427662 | |||||||
| chr9:94427692 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0302 a0001c0001t0001g0314 others(2): Show |
7 | NA18944.hp2 NA18950.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-1497A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427692 | |||||||
| chr9:94427768 | T | A | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.205-1421T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427768 | |||||||
| chr9:94427798 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.205-1391G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427798 | |||||||
| chr9:94427852 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.205-1337A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427852 | |||||||
| chr9:94427976 | G | T | 1 | a0001c0001t0004g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.205-1213G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427976 | |||||||
| chr9:94428039 | C | A | 1 | a0001c0001t0002g0004 | 2 | HG02083.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.205-1150C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428039 | |||||||
| chr9:94428139 | G | T | 2 | a0001c0001t0007g0009 a0001c0001t0007g0010 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.205-1050G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428139 | |||||||
| chr9:94428244 | A | C | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.205-945A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428244 | |||||||
| chr9:94428370 | A | G | 1 | a0001c0001t0007g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.205-819A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428370 | |||||||
| chr9:94428380 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(274): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.205-809G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428380 | |||||||
| chr9:94428421 | C | A | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.205-768C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428421 | |||||||
| chr9:94428488 | G | A | 3 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 |
3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.205-701G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428488 | |||||||
| chr9:94428590 | A | AC | 28 | a0001c0001t0001g0081 a0001c0001t0001g0267 a0001c0001t0001g0303 others(25): Show |
28 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.205-589dupC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94428590 | ||||||
| chr9:94428590 | AC | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(68): Show |
73 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.205-589delC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94428590 | ||||||
| chr9:94428600 | CT | C | 42 | a0001c0001t0001g0260 a0001c0001t0001g0273 a0001c0001t0001g0274 others(39): Show |
42 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.205-577delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94428600 | ||||||
| chr9:94428601 | T | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(54): Show |
59 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.205-588T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428601 | |||||||
| chr9:94428602 | T | C | 8 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(5): Show |
8 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-587T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428602 | |||||||
| chr9:94428815 | G | C | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.205-374G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428815 | |||||||
| chr9:94428959 | A | G | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.205-230A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428959 | |||||||
| chr9:94428992 | A | G | 1 | a0001c0001t0003g0177 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.205-197A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428992 | |||||||
| chr9:94429097 | G | A | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.205-92G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94429097 | |||||||
| chr9:94429336 | T | C | 1 | a0001c0001t0007g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.267+85T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429336 | |||||||
| chr9:94429428 | G | C | 1 | a0001c0001t0001g0332 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.267+177G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429428 | |||||||
| chr9:94429578 | A | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.267+327A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429578 | |||||||
| chr9:94429734 | C | A | 1 | a0001c0001t0002g0152 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267+483C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429734 | |||||||
| chr9:94429736 | G | C | 1 | a0001c0001t0002g0152 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267+485G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429736 | |||||||
| chr9:94429737 | T | G | 1 | a0001c0001t0002g0152 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267+486T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429737 | |||||||
| chr9:94429909 | A | AT | 21 | a0001c0001t0002g0121 a0001c0001t0002g0123 a0001c0001t0002g0124 others(18): Show |
21 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.267+672dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94429909 | ||||||
| chr9:94429909 | A | ATT | 50 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(47): Show |
51 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.267+671_267+672dup others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94429909 | ||||||
| chr9:94429909 | A | T | 1 | a0001c0001t0003g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.267+658A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429909 | |||||||
| chr9:94429912 | T | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.267+661T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429912 | |||||||
| chr9:94429914 | T | A | 15 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(12): Show |
15 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.267+663T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429914 | |||||||
| chr9:94429929 | G | A | 60 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(57): Show |
60 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.267+678G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429929 | |||||||
| chr9:94429992 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.267+741C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429992 | |||||||
| chr9:94430157 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.267+906C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430157 | |||||||
| chr9:94430161 | C | A | 1 | a0001c0001t0002g0216 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.267+910C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430161 | |||||||
| chr9:94430221 | TA | T | 4 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(1): Show |
4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+972delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94430221 | ||||||
| chr9:94430223 | A | AT | 23 | a0001c0001t0001g0090 a0001c0001t0001g0093 a0001c0001t0001g0302 others(20): Show |
23 | HG01243.hp2 HG01496.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.267+989dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94430223 | ||||||
| chr9:94430223 | AT | A | 74 | a0001c0001t0001g0264 a0001c0001t0001g0273 a0001c0001t0002g0029 others(71): Show |
75 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.267+989delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94430223 | ||||||
| chr9:94430325 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.267+1074T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430325 | |||||||
| chr9:94430424 | T | G | 1 | a0001c0002t0020g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.267+1173T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430424 | |||||||
| chr9:94430443 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.267+1192G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430443 | |||||||
| chr9:94430472 | C | T | 3 | a0001c0001t0001g0305 a0001c0001t0001g0333 a0002c0004t0001g0330 |
3 | HG02165.hp2 HG02293.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.267+1221C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430472 | |||||||
| chr9:94430476 | G | A | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.267+1225G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430476 | |||||||
| chr9:94430650 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.267+1399C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430650 | |||||||
| chr9:94430662 | C | G | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.267+1411C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430662 | |||||||
| chr9:94430787 | C | T | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.267+1536C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430787 | |||||||
| chr9:94430856 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+1605G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430856 | |||||||
| chr9:94430888 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.267+1637A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430888 | |||||||
| chr9:94430920 | T | C | 5 | a0001c0001t0001g0261 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG00438.hp2 HG00673.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+1669T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430920 | |||||||
| chr9:94430921 | A | C | 1 | a0001c0001t0004g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.267+1670A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430921 | |||||||
| chr9:94430932 | T | A | 1 | a0001c0001t0002g0152 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267+1681T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430932 | |||||||
| chr9:94431050 | C | T | 2 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
2 | NA18968.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.267+1799C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431050 | |||||||
| chr9:94431051 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.267+1800G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431051 | |||||||
| chr9:94431172 | T | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.267+1921T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431172 | |||||||
| chr9:94431271 | C | T | 17 | a0001c0001t0002g0183 a0001c0001t0002g0210 a0001c0001t0003g0149 others(14): Show |
17 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.267+2020C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431271 | |||||||
| chr9:94431312 | CA | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(20): Show |
24 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.267+2077delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94431312 | ||||||
| chr9:94431321 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.267+2070A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431321 | |||||||
| chr9:94431329 | T | A | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.267+2078T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431329 | |||||||
| chr9:94431369 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.267+2118G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431369 | |||||||
| chr9:94431430 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.267+2179A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431430 | |||||||
| chr9:94431516 | C | CT | 50 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(47): Show |
50 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.267+2275dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94431516 | ||||||
| chr9:94431576 | A | T | 1 | a0001c0001t0001g0332 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.267+2325A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431576 | |||||||
| chr9:94431719 | A | G | 40 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(37): Show |
40 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.267+2468A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431719 | |||||||
| chr9:94431752 | A | AC | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.267+2506dupC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94431752 | ||||||
| chr9:94431753 | C | A | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.267+2502C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431753 | |||||||
| chr9:94431941 | T | C | 1 | a0001c0001t0004g0071 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.267+2690T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431941 | |||||||
| chr9:94432032 | C | T | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.267+2781C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432032 | |||||||
| chr9:94432095 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(179): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.267+2844G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432095 | |||||||
| chr9:94432194 | A | G | 1 | a0001c0001t0004g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.267+2943A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432194 | |||||||
| chr9:94432238 | C | G | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.267+2987C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432238 | |||||||
| chr9:94432252 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(89): Show |
94 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.267+3001G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432252 | |||||||
| chr9:94432378 | T | A | 1 | a0001c0001t0003g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.267+3127T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432378 | |||||||
| chr9:94432399 | C | G | 1 | a0001c0001t0005g0018 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.267+3148C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432399 | |||||||
| chr9:94432454 | C | G | 1 | a0001c0001t0007g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.267+3203C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432454 | |||||||
| chr9:94432480 | A | G | 19 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0126 others(16): Show |
19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.267+3229A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432480 | |||||||
| chr9:94432710 | G | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.267+3459G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432710 | |||||||
| chr9:94432837 | C | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.267+3586C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432837 | |||||||
| chr9:94432852 | C | T | 4 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(1): Show |
4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+3601C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432852 | |||||||
| chr9:94432997 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.267+3746G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432997 | |||||||
| chr9:94433031 | T | C | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.267+3780T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433031 | |||||||
| chr9:94433035 | G | A | 1 | a0001c0001t0003g0211 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.267+3784G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433035 | |||||||
| chr9:94433134 | CTG | C | 56 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(53): Show |
57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.267+3884_267+3885d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433134 | |||||||
| chr9:94433251 | C | T | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.267+4000C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433251 | |||||||
| chr9:94433347 | A | G | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(1): Show |
4 | HG00140.hp1 HG01074.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+4096A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433347 | |||||||
| chr9:94433372 | T | TA | 91 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(88): Show |
93 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.267+4129dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94433372 | ||||||
| chr9:94433381 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(241): Show |
248 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.267+4130G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433381 | |||||||
| chr9:94433394 | C | T | 32 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.267+4143C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433394 | |||||||
| chr9:94433491 | C | T | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.267+4240C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433491 | |||||||
| chr9:94433539 | G | A | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.267+4288G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433539 | |||||||
| chr9:94433612 | A | G | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.267+4361A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433612 | |||||||
| chr9:94433617 | C | T | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.267+4366C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433617 | |||||||
| chr9:94433697 | T | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+4446T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433697 | |||||||
| chr9:94433950 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.268-4451A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433950 | |||||||
| chr9:94434084 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0097 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.268-4317A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434084 | |||||||
| chr9:94434475 | C | A | 1 | a0001c0001t0001g0333 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.268-3926C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434475 | |||||||
| chr9:94434479 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.268-3922G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434479 | |||||||
| chr9:94434505 | C | T | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.268-3896C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434505 | |||||||
| chr9:94434560 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.268-3841C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434560 | |||||||
| chr9:94434580 | G | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.268-3821G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434580 | |||||||
| chr9:94434605 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.268-3796G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434605 | |||||||
| chr9:94434697 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.268-3704A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434697 | |||||||
| chr9:94434708 | C | A | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.268-3693C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434708 | |||||||
| chr9:94434728 | T | C | 3 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 |
3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.268-3673T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434728 | |||||||
| chr9:94434987 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.268-3414A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434987 | |||||||
| chr9:94434998 | C | A | 1 | a0001c0001t0001g0268 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.268-3403C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434998 | |||||||
| chr9:94435267 | A | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.268-3134A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435267 | |||||||
| chr9:94435427 | C | T | 19 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0126 others(16): Show |
19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.268-2974C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435427 | |||||||
| chr9:94435510 | A | G | 1 | a0001c0001t0005g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.268-2891A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435510 | |||||||
| chr9:94435643 | CCTT | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0256 others(52): Show |
58 | HG00323.hp2 HG00673.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.268-2751_268-2749d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435643 | ||||||
| chr9:94435647 | CTTCTTTT others(2): Show |
C | 8 | a0001c0001t0001g0273 a0001c0001t0001g0281 a0001c0001t0001g0282 others(5): Show |
8 | HG00423.hp1 HG00423.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.268-2751_268-2743d others(11): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435647 | ||||||
| chr9:94435648 | TTC | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(105): Show |
109 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.268-2751_268-2750d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435648 | ||||||
| chr9:94435649 | TC | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-2751delC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435649 | |||||||
| chr9:94435650 | C | CT | 22 | a0001c0001t0002g0109 a0001c0001t0002g0126 a0001c0001t0002g0127 others(19): Show |
22 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.268-2730dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435650 | ||||||
| chr9:94435650 | C | CTT | 9 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0113 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.268-2731_268-2730d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435650 | ||||||
| chr9:94435650 | C | T | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.268-2751C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435650 | |||||||
| chr9:94435650 | CT | C | 6 | a0001c0001t0002g0135 a0001c0001t0002g0167 a0001c0001t0006g0106 others(3): Show |
6 | HG01256.hp2 HG01517.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-2730delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435650 | ||||||
| chr9:94435740 | C | T | 5 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0015 others(2): Show |
5 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-2661C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435740 | |||||||
| chr9:94435741 | G | A | 1 | a0001c0001t0004g0045 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.268-2660G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435741 | |||||||
| chr9:94435779 | C | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.268-2622C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435779 | |||||||
| chr9:94435933 | G | C | 1 | a0001c0001t0007g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.268-2468G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435933 | |||||||
| chr9:94435970 | GCTTT | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.268-2426_268-2423d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435970 | ||||||
| chr9:94436102 | T | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.268-2299T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436102 | |||||||
| chr9:94436510 | T | G | 52 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.268-1891T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436510 | |||||||
| chr9:94436533 | T | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0088 |
3 | HG00642.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.268-1868T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436533 | |||||||
| chr9:94436691 | C | A | 1 | a0001c0001t0003g0199 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.268-1710C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436691 | |||||||
| chr9:94436831 | T | A | 1 | a0001c0001t0002g0152 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.268-1570T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436831 | |||||||
| chr9:94436890 | A | G | 1 | a0001c0001t0003g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.268-1511A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436890 | |||||||
| chr9:94437265 | C | G | 52 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.268-1136C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437265 | |||||||
| chr9:94437357 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.268-1044C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437357 | |||||||
| chr9:94437364 | G | A | 1 | a0001c0001t0004g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.268-1037G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437364 | |||||||
| chr9:94437370 | C | T | 60 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(57): Show |
60 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.268-1031C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437370 | |||||||
| chr9:94437464 | T | C | 1 | a0001c0001t0001g0341 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.268-937T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437464 | |||||||
| chr9:94437571 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.268-830C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437571 | |||||||
| chr9:94437803 | G | A | 7 | a0001c0001t0005g0002 a0001c0001t0005g0030 a0001c0001t0005g0031 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.268-598G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437803 | |||||||
| chr9:94437817 | T | C | 1 | a0001c0001t0002g0168 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.268-584T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437817 | |||||||
| chr9:94437928 | T | C | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268-473T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437928 | |||||||
| chr9:94438132 | T | A | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.268-269T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94438132 | |||||||
| chr9:94438135 | A | G | 1 | a0001c0001t0007g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.268-266A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94438135 | |||||||
| chr9:94438216 | G | T | 1 | a0001c0001t0003g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.268-185G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94438216 | |||||||
| chr9:94438908 | C | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.395+380C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438908 | |||||||
| chr9:94438909 | G | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.395+381G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438909 | |||||||
| chr9:94438916 | G | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.395+388G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438916 | |||||||
| chr9:94438947 | T | C | 19 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0126 others(16): Show |
19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.395+419T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438947 | |||||||
| chr9:94438952 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.395+424G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438952 | |||||||
| chr9:94438977 | A | G | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+449A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438977 | |||||||
| chr9:94439022 | G | GT | 20 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0110 others(17): Show |
20 | HG00099.hp1 HG00597.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.395+510dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | ||||||
| chr9:94439022 | G | GTTTTTT | 54 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(51): Show |
56 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.395+505_395+510dup others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | ||||||
| chr9:94439022 | G | GTTTTTTT | 52 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0091 others(49): Show |
53 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.395+504_395+510dup others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | ||||||
| chr9:94439022 | G | GTTTTTTT others(1): Show |
38 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(35): Show |
39 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.395+503_395+510dup others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | ||||||
| chr9:94439022 | G | GTTTTTTT others(2): Show |
26 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0004g0028 others(23): Show |
26 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.395+502_395+510dup others(9): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | ||||||
| chr9:94439022 | G | GTTTTTTT others(3): Show |
3 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0004g0063 |
3 | HG01358.hp1 HG02559.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.395+501_395+510dup others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | ||||||
| chr9:94439068 | CTGGA | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.395+541_395+544del others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439068 | |||||||
| chr9:94439166 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0301 |
2 | NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.395+638C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439166 | |||||||
| chr9:94439268 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.395+740A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439268 | |||||||
| chr9:94439272 | GCTGGGAT others(19): Show |
G | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.395+745_395+770del others(26): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439272 | |||||||
| chr9:94439309 | A | AT | 26 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(23): Show |
27 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.395+796dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439309 | ||||||
| chr9:94439309 | AT | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(98): Show |
103 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.395+796delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439309 | ||||||
| chr9:94439309 | ATT | A | 51 | a0001c0001t0001g0338 a0001c0001t0004g0027 a0001c0001t0004g0028 others(48): Show |
52 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.395+795_395+796del others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439309 | ||||||
| chr9:94439321 | T | TC | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.395+793_395+794ins others(1): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439321 | |||||||
| chr9:94439438 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.395+910A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439438 | |||||||
| chr9:94439542 | A | AT | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0083 others(168): Show |
175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.395+1029dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439542 | ||||||
| chr9:94439542 | A | ATT | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG00323.hp1 HG01358.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.395+1028_395+1029d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439542 | ||||||
| chr9:94439757 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.396-1228A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439757 | |||||||
| chr9:94439918 | C | T | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.396-1067C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439918 | |||||||
| chr9:94440119 | T | C | 2 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
2 | NA18968.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.396-866T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94440119 | |||||||
| chr9:94440176 | C | T | 5 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0015 others(2): Show |
5 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-809C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94440176 | |||||||
| chr9:94440214 | C | T | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.396-771C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94440214 | |||||||
| chr9:94440299 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.396-686G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94440299 | |||||||
| chr9:94440303 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.396-682A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94440303 | |||||||
| chr9:94441243 | G | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.510+144G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441243 | |||||||
| chr9:94441347 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.510+248A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441347 | |||||||
| chr9:94441381 | A | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+282A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441381 | |||||||
| chr9:94441384 | A | G | 1 | a0001c0001t0007g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.510+285A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441384 | |||||||
| chr9:94441506 | A | G | 52 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.510+407A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441506 | |||||||
| chr9:94441611 | G | T | 1 | a0001c0001t0001g0329 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.510+512G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441611 | |||||||
| chr9:94441721 | G | C | 1 | a0001c0001t0002g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.510+622G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441721 | |||||||
| chr9:94441728 | AT | A | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+632delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr9 | 94441728 | ||||||
| chr9:94441758 | C | T | 5 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0015 others(2): Show |
5 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+659C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441758 | |||||||
| chr9:94441807 | G | T | 2 | a0001c0001t0004g0053 a0001c0001t0004g0054 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.510+708G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441807 | |||||||
| chr9:94441848 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.510+749G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441848 | |||||||
| chr9:94442321 | A | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.510+1222A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442321 | |||||||
| chr9:94442322 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.510+1223C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442322 | |||||||
| chr9:94442396 | C | T | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.510+1297C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442396 | |||||||
| chr9:94442525 | A | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(15): Show |
19 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.510+1426A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442525 | |||||||
| chr9:94442578 | C | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.510+1479C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442578 | |||||||
| chr9:94442588 | C | T | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+1489C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442588 | |||||||
| chr9:94442619 | G | A | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+1520G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442619 | |||||||
| chr9:94442657 | C | T | 1 | a0001c0001t0003g0191 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.510+1558C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442657 | |||||||
| chr9:94442679 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.510+1580C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442679 | |||||||
| chr9:94442688 | T | TA | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.510+1593dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr9 | 94442688 | ||||||
| chr9:94442723 | G | A | 9 | a0001c0001t0002g0183 a0001c0001t0003g0149 a0001c0001t0003g0154 others(6): Show |
9 | HG00544.hp2 NA18747.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+1624G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442723 | |||||||
| chr9:94442830 | C | T | 19 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0126 others(16): Show |
19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.510+1731C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442830 | |||||||
| chr9:94442856 | A | C | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.510+1757A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442856 | |||||||
| chr9:94442938 | G | C | 24 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0047 others(21): Show |
24 | HG00597.hp1 HG00639.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+1839G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442938 | |||||||
| chr9:94443138 | C | G | 1 | a0001c0001t0017g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.511-1826C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94443138 | |||||||
| chr9:94443264 | C | T | 52 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.511-1700C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94443264 | |||||||
| chr9:94443504 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.511-1460C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94443504 | |||||||
| chr9:94443538 | CACTT | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.511-1422_511-1419d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr9 | 94443538 | ||||||
| chr9:94443851 | C | T | 4 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(1): Show |
4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-1113C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94443851 | |||||||
| chr9:94444132 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.511-832T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444132 | |||||||
| chr9:94444146 | A | G | 1 | a0001c0001t0005g0077 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.511-818A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444146 | |||||||
| chr9:94444333 | C | G | 4 | a0001c0001t0004g0035 a0001c0001t0004g0037 a0001c0001t0004g0038 others(1): Show |
4 | HG02896.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-631C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444333 | |||||||
| chr9:94444348 | C | T | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.511-616C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444348 | |||||||
| chr9:94444455 | G | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.511-509G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444455 | |||||||
| chr9:94444674 | G | A | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.511-290G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444674 | |||||||
| chr9:94444869 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(83): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.511-95G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444869 | |||||||
| chr9:94445311 | T | A | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.729+129T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445311 | |||||||
| chr9:94445387 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.729+205G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445387 | |||||||
| chr9:94445718 | T | C | 1 | a0001c0001t0002g0128 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.729+536T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445718 | |||||||
| chr9:94445769 | GAA | G | 5 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(2): Show |
5 | HG02818.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.729+595_729+596del others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr9 | 94445769 | ||||||
| chr9:94445770 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG00323.hp1 HG02559.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.729+588A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445770 | |||||||
| chr9:94445868 | A | T | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.729+686A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445868 | |||||||
| chr9:94445943 | A | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.729+761A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445943 | |||||||
| chr9:94445949 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.729+767A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445949 | |||||||
| chr9:94446035 | T | C | 52 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.730-788T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446035 | |||||||
| chr9:94446111 | G | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.730-712G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446111 | |||||||
| chr9:94446273 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0098 |
2 | HG00733.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.730-550C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446273 | |||||||
| chr9:94446312 | A | T | 1 | a0001c0001t0002g0173 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.730-511A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446312 | |||||||
| chr9:94446345 | C | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(123): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.730-478C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446345 | |||||||
| chr9:94446417 | C | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(178): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.730-406C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446417 | |||||||
| chr9:94446422 | C | T | 1 | a0001c0001t0004g0075 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.730-401C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446422 | |||||||
| chr9:94446428 | C | T | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.730-395C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446428 | |||||||
| chr9:94446641 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.730-182T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446641 | |||||||
| chr9:94446678 | A | G | 1 | a0001c0001t0002g0004 | 2 | HG02083.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.730-145A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446678 | |||||||
| chr9:94446701 | A | G | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0208 others(1): Show |
4 | HG00140.hp1 HG01074.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-122A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446701 | |||||||
| chr9:94446784 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.730-39T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446784 | |||||||
| chr9:94447085 | A | C | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.843+149A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447085 | |||||||
| chr9:94447171 | A | T | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.843+235A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447171 | |||||||
| chr9:94447183 | C | CT | 40 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(37): Show |
40 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.843+260dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447183 | ||||||
| chr9:94447183 | CT | C | 14 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0003g0186 others(11): Show |
14 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.843+260delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447183 | ||||||
| chr9:94447258 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0019g0137 |
2 | HG01255.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.843+322C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447258 | |||||||
| chr9:94447325 | G | A | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.843+389G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447325 | |||||||
| chr9:94447331 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.843+395T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447331 | |||||||
| chr9:94447379 | C | T | 6 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0167 others(3): Show |
6 | NA18948.hp2 NA18957.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+443C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447379 | |||||||
| chr9:94447380 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | HG02258.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.843+444G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447380 | |||||||
| chr9:94447392 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.843+456T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447392 | |||||||
| chr9:94447438 | C | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.843+502C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447438 | |||||||
| chr9:94447479 | CTG | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0081 others(38): Show |
42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.843+545_843+546del others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447479 | ||||||
| chr9:94447480 | TG | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0093 |
3 | HG01358.hp1 HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.843+545delG | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447480 | |||||||
| chr9:94447481 | G | GT | 8 | a0001c0001t0002g0179 a0001c0001t0002g0217 a0001c0001t0002g0255 others(5): Show |
8 | HG02055.hp2 HG02300.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.843+565dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447481 | ||||||
| chr9:94447481 | GT | G | 14 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0338 others(11): Show |
14 | HG01081.hp2 HG01109.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.843+565delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447481 | ||||||
| chr9:94447481 | GTT | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0257 a0001c0001t0001g0259 others(134): Show |
139 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.843+564_843+565del others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447481 | ||||||
| chr9:94447605 | T | C | 1 | a0001c0001t0003g0196 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.843+669T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447605 | |||||||
| chr9:94447626 | G | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+690G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447626 | |||||||
| chr9:94447694 | T | A | 52 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.843+758T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447694 | |||||||
| chr9:94447753 | C | T | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.843+817C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447753 | |||||||
| chr9:94448107 | T | TA | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.843+1173dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94448107 | ||||||
| chr9:94448242 | G | A | 1 | a0001c0001t0004g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.843+1306G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448242 | |||||||
| chr9:94448308 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.843+1372C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448308 | |||||||
| chr9:94448363 | AC | A | 36 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(33): Show |
36 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.843+1429delC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94448363 | ||||||
| chr9:94448463 | G | C | 1 | a0001c0001t0005g0018 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.843+1527G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448463 | |||||||
| chr9:94448605 | T | C | 2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.843+1669T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448605 | |||||||
| chr9:94448610 | C | T | 52 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.843+1674C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448610 | |||||||
| chr9:94448715 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.843+1779C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448715 | |||||||
| chr9:94448783 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.843+1847C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448783 | |||||||
| chr9:94448789 | C | T | 1 | a0002c0004t0001g0330 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.843+1853C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448789 | |||||||
| chr9:94449030 | T | C | 3 | a0001c0002t0008g0240 a0001c0002t0008g0244 a0001c0002t0008g0245 |
3 | HG01255.hp2 HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.843+2094T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449030 | |||||||
| chr9:94449160 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.843+2224A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449160 | |||||||
| chr9:94449374 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.844-2082A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449374 | |||||||
| chr9:94449434 | T | C | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.844-2022T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449434 | |||||||
| chr9:94449467 | AG | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0338 a0001c0001t0001g0340 |
5 | NA18944.hp2 NA18950.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-1987delG | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94449467 | ||||||
| chr9:94449502 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.844-1954C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449502 | |||||||
| chr9:94449612 | A | G | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.844-1844A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449612 | |||||||
| chr9:94449734 | A | G | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.844-1722A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449734 | |||||||
| chr9:94449778 | A | G | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.844-1678A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449778 | |||||||
| chr9:94449914 | A | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(23): Show |
27 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.844-1542A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449914 | |||||||
| chr9:94449976 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.844-1480G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449976 | |||||||
| chr9:94450042 | G | A | 2 | a0001c0001t0006g0106 a0001c0001t0006g0108 |
2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.844-1414G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450042 | |||||||
| chr9:94450176 | A | G | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 |
3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.844-1280A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450176 | |||||||
| chr9:94450315 | T | C | 1 | a0001c0001t0001g0319 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.844-1141T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450315 | |||||||
| chr9:94450341 | G | A | 3 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 |
3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.844-1115G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450341 | |||||||
| chr9:94450437 | T | C | 1 | a0001c0001t0006g0254 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.844-1019T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450437 | |||||||
| chr9:94450440 | C | T | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.844-1016C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450440 | |||||||
| chr9:94450492 | A | AACTT | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-964_844-963ins others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450492 | |||||||
| chr9:94450493 | C | CTTTTTTT others(3): Show |
11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.844-958_844-949dup others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | ||||||
| chr9:94450493 | C | CTTTTTTT others(5): Show |
23 | a0001c0001t0004g0047 a0001c0001t0004g0060 a0001c0001t0005g0002 others(20): Show |
24 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.844-960_844-949dup others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | ||||||
| chr9:94450493 | C | CTTTTTTT others(6): Show |
34 | a0001c0001t0001g0256 a0001c0001t0002g0248 a0001c0001t0002g0249 others(31): Show |
34 | HG00597.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.844-961_844-949dup others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | ||||||
| chr9:94450493 | C | CTTTTTTT others(7): Show |
71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0083 others(68): Show |
74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.844-962_844-949dup others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | ||||||
| chr9:94450493 | C | CTTTTTTT others(8): Show |
43 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0088 others(40): Show |
43 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | ||||||
| chr9:94450493 | C | CTTTTTTT others(9): Show |
13 | a0001c0001t0001g0081 a0001c0001t0001g0261 a0001c0001t0001g0274 others(10): Show |
13 | HG01081.hp1 HG01106.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(16): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | ||||||
| chr9:94450493 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0007g0010 a0001c0001t0007g0011 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.844-949_844-948ins others(17): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | ||||||
| chr9:94450493 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0079 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.844-949_844-948ins others(22): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | ||||||
| chr9:94450493 | C | T | 9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-963C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450493 | |||||||
| chr9:94450507 | T | TTTTTTTT others(6): Show |
1 | a0001c0001t0002g0133 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.844-949_844-948ins others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450507 | T | TTTTTTTT others(7): Show |
1 | a0001c0001t0002g0124 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.844-949_844-948ins others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450507 | T | TTTTTTTT others(11): Show |
1 | a0001c0001t0003g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.844-949_844-948ins others(18): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450507 | T | TTTTTTTT others(12): Show |
2 | a0001c0001t0002g0136 a0001c0001t0003g0008 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.844-949_844-948ins others(19): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450507 | T | TTTTTTTT others(13): Show |
5 | a0001c0001t0002g0120 a0001c0001t0002g0122 a0001c0001t0002g0125 others(2): Show |
5 | HG01255.hp1 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(20): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450507 | T | TTTTTTTT others(14): Show |
6 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0135 others(3): Show |
6 | HG01243.hp1 HG01256.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(21): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450507 | T | TTTTTTTT others(15): Show |
6 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0139 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(22): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450507 | T | TTTTTTTT others(16): Show |
7 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0121 others(4): Show |
7 | HG00639.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(23): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450507 | T | TTTTTTTT others(17): Show |
3 | a0001c0001t0002g0123 a0001c0001t0002g0126 a0001c0001t0002g0140 |
3 | HG01109.hp2 NA18978.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.844-949_844-948ins others(24): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450507 | T | TTTTTTTT others(18): Show |
2 | a0001c0001t0002g0131 a0001c0001t0002g0138 |
2 | NA19057.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.844-949_844-948ins others(25): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450507 | T | TTTTTTTT others(19): Show |
2 | a0001c0001t0002g0132 a0001c0001t0002g0252 |
2 | HG02015.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.844-949_844-948ins others(26): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | |||||||
| chr9:94450540 | A | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.844-916A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450540 | |||||||
| chr9:94450651 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(231): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.844-805A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450651 | |||||||
| chr9:94450687 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.844-769C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450687 | |||||||
| chr9:94450688 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.844-768G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450688 | |||||||
| chr9:94450917 | C | T | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.844-539C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450917 | |||||||
| chr9:94450986 | G | A | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.844-470G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450986 | |||||||
| chr9:94451162 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.844-294A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94451162 | |||||||
| chr9:94451201 | A | G | 13 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(10): Show |
13 | HG01243.hp1 HG01255.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.844-255A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94451201 | |||||||
| chr9:94451223 | A | G | 1 | a0001c0001t0004g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.844-233A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94451223 | |||||||
| chr9:94451265 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.844-191G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94451265 | |||||||
| chr9:94451278 | G | A | 40 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(37): Show |
40 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.844-178G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94451278 | |||||||
| chr9:94451436 | TTTTCA | T | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.844-10_844-6delATT others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94451436 | ||||||
| chr9:94451561 | A | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.915+34A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94451561 | |||||||
| chr9:94451652 | C | G | 1 | a0001c0001t0017g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.915+125C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94451652 | |||||||
| chr9:94451936 | G | A | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+409G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94451936 | |||||||
| chr9:94452324 | C | T | 1 | a0001c0001t0015g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.915+797C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452324 | |||||||
| chr9:94452468 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.915+941G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452468 | |||||||
| chr9:94452594 | C | A | 36 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(33): Show |
36 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.915+1067C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452594 | |||||||
| chr9:94452614 | A | AAT | 49 | a0001c0001t0002g0157 a0001c0001t0002g0248 a0001c0001t0002g0250 others(46): Show |
49 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.915+1104_915+1105d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452614 | ||||||
| chr9:94452614 | AAT | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.915+1104_915+1105d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452614 | ||||||
| chr9:94452630 | TATTTTCA others(21): Show |
T | 1 | a0001c0001t0002g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.915+1106_915+1133d others(30): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452630 | ||||||
| chr9:94452632 | T | C | 1 | a0001c0001t0003g0156 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.915+1105T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452632 | |||||||
| chr9:94452635 | TCATATAT others(23): Show |
T | 6 | a0001c0001t0004g0038 a0001c0001t0005g0002 a0001c0001t0005g0030 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.915+1109_915+1138d others(32): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452635 | |||||||
| chr9:94452638 | TATATATA others(3): Show |
T | 6 | a0001c0001t0002g0170 a0001c0001t0003g0203 a0001c0001t0003g0204 others(3): Show |
6 | HG01346.hp1 HG04228.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+1148_915+1157d others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452638 | ||||||
| chr9:94452638 | TATATATA others(41): Show |
T | 7 | a0001c0001t0004g0047 a0001c0001t0004g0048 a0001c0001t0004g0049 others(4): Show |
7 | NA18995.hp2 NA19000.hp2 NA19001.hp2 others(4): Show |
intron_variant | MODIFIER | c.915+1128_915+1175d others(50): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452638 | ||||||
| chr9:94452640 | TATATATT others(31): Show |
T | 89 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0002g0029 others(86): Show |
89 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.915+1138_915+1175d others(40): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452640 | ||||||
| chr9:94452650 | TATATATT others(21): Show |
T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0083 others(133): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.915+1148_915+1175d others(30): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452650 | ||||||
| chr9:94452650 | TATATATT others(39): Show |
T | 1 | a0001c0001t0004g0057 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.915+1150_915+1195d others(48): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452650 | ||||||
| chr9:94452658 | CAT | C | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.915+1138_915+1139d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452658 | ||||||
| chr9:94452658 | CATATATA others(41): Show |
C | 1 | a0001c0001t0004g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.915+1138_915+1185d others(50): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452658 | ||||||
| chr9:94452660 | T | TATATATT others(11): Show |
1 | a0001c0001t0003g0187 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.915+1176_915+1193d others(20): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452660 | ||||||
| chr9:94452660 | TATATATT others(11): Show |
T | 1 | a0001c0001t0001g0321 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.915+1176_915+1193d others(20): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452660 | ||||||
| chr9:94452665 | A | T | 1 | a0001c0001t0002g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.915+1138A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452665 | |||||||
| chr9:94452672 | TATATTC | T | 7 | a0001c0001t0002g0249 a0001c0001t0004g0038 a0001c0001t0005g0002 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+1150_915+1155d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452672 | ||||||
| chr9:94452679 | ATATATTC others(61): Show |
A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.915+1156_916-1208d others(70): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452679 | ||||||
| chr9:94452715 | ATATATAT others(25): Show |
A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.915+1192_916-1208d others(34): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452715 | ||||||
| chr9:94452758 | A | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(20): Show |
24 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.916-1200A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452758 | |||||||
| chr9:94453042 | C | T | 52 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.916-916C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453042 | |||||||
| chr9:94453052 | T | A | 8 | a0001c0002t0008g0239 a0001c0002t0008g0240 a0001c0002t0008g0241 others(5): Show |
8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-906T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453052 | |||||||
| chr9:94453094 | C | A | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.916-864C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453094 | |||||||
| chr9:94453109 | A | G | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.916-849A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453109 | |||||||
| chr9:94453139 | C | G | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.916-819C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453139 | |||||||
| chr9:94453148 | C | CT | 8 | a0001c0001t0002g0171 a0001c0001t0002g0181 a0001c0001t0002g0216 others(5): Show |
8 | HG01192.hp1 HG01516.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.916-791dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94453148 | ||||||
| chr9:94453148 | CT | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0079 a0001c0001t0001g0080 others(98): Show |
103 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.916-791delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94453148 | ||||||
| chr9:94453148 | CTT | C | 120 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(117): Show |
121 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.916-792_916-791del others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94453148 | ||||||
| chr9:94453175 | A | G | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.916-783A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453175 | |||||||
| chr9:94453184 | CTGTCACC others(10): Show |
C | 32 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(29): Show |
32 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.916-771_916-755del others(17): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94453184 | ||||||
| chr9:94453335 | C | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(184): Show |
191 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.916-623C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453335 | |||||||
| chr9:94453336 | G | A | 2 | a0001c0001t0003g0247 a0001c0001t0003g0253 |
2 | HG01346.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.916-622G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453336 | |||||||
| chr9:94453342 | G | T | 1 | a0001c0001t0004g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.916-616G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453342 | |||||||
| chr9:94453479 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(184): Show |
191 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.916-479A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453479 | |||||||
| chr9:94453562 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.916-396C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453562 | |||||||
| chr9:94453694 | C | T | 2 | a0001c0001t0007g0009 a0001c0001t0007g0010 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.916-264C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453694 | |||||||
| chr9:94453760 | G | T | 1 | a0001c0001t0001g0327 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.916-198G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453760 | |||||||
| chr9:94453881 | G | T | 52 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.916-77G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453881 | |||||||
| chr9:94454170 | G | C | 1 | a0001c0001t0001g0340 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1028+100G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454170 | |||||||
| chr9:94454235 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1028+165A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454235 | |||||||
| chr9:94454259 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1028+189A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454259 | |||||||
| chr9:94454391 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(86): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1028+321G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454391 | |||||||
| chr9:94454416 | G | T | 1 | a0001c0001t0003g0186 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1028+346G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454416 | |||||||
| chr9:94454496 | T | G | 1 | a0001c0001t0021g0231 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1028+426T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454496 | |||||||
| chr9:94454529 | G | GCTAATTT others(300): Show |
9 | a0001c0001t0006g0101 a0001c0001t0006g0102 a0001c0001t0006g0103 others(6): Show |
9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1028+476_1028+477i others(309): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94454529 | ||||||
| chr9:94454568 | G | A | 52 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(49): Show |
53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1028+498G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454568 | |||||||
| chr9:94454737 | A | G | 3 | a0001c0001t0001g0299 a0001c0001t0001g0303 a0001c0001t0001g0304 |
3 | NA18939.hp1 NA18956.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1028+667A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454737 | |||||||
| chr9:94454739 | G | C | 67 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(64): Show |
67 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1028+669G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454739 | |||||||
| chr9:94454752 | A | G | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 |
3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1028+682A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454752 | |||||||
| chr9:94454957 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1028+887G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454957 | |||||||
| chr9:94454982 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(172): Show |
179 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1028+912G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454982 | |||||||
| chr9:94454993 | G | A | 51 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(48): Show |
52 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1028+923G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454993 | |||||||
| chr9:94455002 | A | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1028+932A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455002 | |||||||
| chr9:94455039 | A | G | 2 | a0001c0001t0001g0260 a0001c0001t0016g0022 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1028+969A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455039 | |||||||
| chr9:94455118 | C | A | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0014g0006 |
3 | HG00639.hp1 HG01109.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1028+1048C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455118 | |||||||
| chr9:94455156 | C | CT | 55 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0259 others(52): Show |
55 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1029-1059dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTT | 17 | a0001c0001t0001g0260 a0001c0001t0001g0268 a0001c0001t0001g0276 others(14): Show |
17 | HG00323.hp2 HG01071.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1029-1060_1029-105 others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTT | 35 | a0001c0001t0001g0001 a0001c0001t0001g0273 a0001c0001t0001g0275 others(32): Show |
37 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1029-1061_1029-105 others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTT | 26 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(23): Show |
27 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1029-1062_1029-105 others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTTTT | 11 | a0001c0001t0001g0090 a0001c0001t0001g0093 a0001c0001t0001g0323 others(8): Show |
11 | HG00408.hp2 HG01256.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1029-1064_1029-105 others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTTTTT others(1): Show |
16 | a0001c0001t0002g0123 a0001c0001t0002g0126 a0001c0001t0002g0127 others(13): Show |
16 | HG00639.hp1 HG01109.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1029-1066_1029-105 others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTTTTT others(2): Show |
16 | a0001c0001t0001g0089 a0001c0001t0001g0327 a0001c0001t0002g0124 others(13): Show |
16 | HG00597.hp1 HG02572.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.1029-1067_1029-105 others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTTTTT others(3): Show |
7 | a0001c0001t0004g0042 a0001c0001t0004g0048 a0001c0001t0004g0057 others(4): Show |
7 | HG01099.hp2 HG02148.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1029-1068_1029-105 others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTTTTT others(4): Show |
8 | a0001c0001t0002g0122 a0001c0001t0004g0069 a0001c0001t0005g0020 others(5): Show |
8 | HG00642.hp1 HG01109.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-1069_1029-105 others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTTTTT others(5): Show |
12 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0121 others(9): Show |
13 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1029-1070_1029-105 others(16): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTTTTT others(6): Show |
8 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0120 others(5): Show |
8 | HG01243.hp1 HG02040.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-1071_1029-105 others(17): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0005g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1029-1072_1029-105 others(18): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0005g0077 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1029-1073_1029-105 others(19): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455156 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0003g0007 a0001c0001t0003g0008 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1029-1081_1029-105 others(27): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | ||||||
| chr9:94455169 | TTTTTTTT others(7): Show |
T | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1029-1070_1029-105 others(18): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455169 | |||||||
| chr9:94455172 | TTTTTTTT others(4): Show |
T | 2 | a0001c0001t0006g0105 a0001c0001t0006g0254 |
2 | HG00544.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1029-1067_1029-105 others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455172 | |||||||
| chr9:94455182 | G | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(235): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1029-1058G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455182 | |||||||
| chr9:94455183 | A | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(235): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1029-1057A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455183 | |||||||
| chr9:94455317 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1029-923C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455317 | |||||||
| chr9:94455338 | T | A | 4 | a0001c0001t0007g0014 a0001c0001t0007g0015 a0001c0001t0007g0016 others(1): Show |
4 | HG01081.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-902T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455338 | |||||||
| chr9:94455338 | T | C | 1 | a0001c0001t0002g0144 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1029-902T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455338 | |||||||
| chr9:94455343 | A | AT | 53 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(50): Show |
53 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1029-887dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455343 | ||||||
| chr9:94455369 | A | T | 36 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(33): Show |
36 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1029-871A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455369 | |||||||
| chr9:94455378 | A | AT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0088 others(20): Show |
25 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.1029-842dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94455378 | A | ATTTT | 16 | a0001c0001t0004g0035 a0001c0001t0004g0037 a0001c0001t0004g0047 others(13): Show |
17 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1029-845_1029-842d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94455378 | A | ATTTTT | 35 | a0001c0001t0001g0260 a0001c0001t0001g0339 a0001c0001t0001g0341 others(32): Show |
35 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1029-846_1029-842d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94455378 | A | ATTTTTT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0257 others(73): Show |
78 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1029-847_1029-842d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94455378 | A | ATTTTTTT | 11 | a0001c0001t0001g0274 a0001c0001t0001g0289 a0001c0001t0001g0293 others(8): Show |
11 | HG00621.hp1 HG02148.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1029-848_1029-842d others(9): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94455378 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG00323.hp1 HG02559.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1029-855_1029-842d others(16): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94455378 | A | ATTTTTTT others(8): Show |
2 | a0001c0001t0012g0023 a0001c0001t0012g0024 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1029-856_1029-842d others(17): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94455378 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1029-858_1029-842d others(19): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94455378 | AT | A | 34 | a0001c0001t0002g0029 a0001c0001t0002g0036 a0001c0001t0002g0039 others(31): Show |
34 | HG00544.hp1 HG00741.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1029-842delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94455378 | ATT | A | 24 | a0001c0001t0002g0121 a0001c0001t0002g0123 a0001c0001t0002g0124 others(21): Show |
24 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.1029-843_1029-842d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94455378 | ATTTTTT | A | 6 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0091 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1029-847_1029-842d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | ||||||
| chr9:94456060 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1029-180C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94456060 | |||||||
| chr9:94456364 | T | C | 1 | a0001c0001t0007g0013 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1126+27T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94456364 | |||||||
| chr9:94456611 | TTTC | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(122): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1126+280_1126+282d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94456611 | ||||||
| chr9:94456774 | T | C | 1 | a0001c0001t0003g0205 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1126+437T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94456774 | |||||||
| chr9:94456792 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1126+455G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94456792 | |||||||
| chr9:94456834 | A | G | 1 | a0001c0001t0016g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1126+497A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94456834 | |||||||
| chr9:94456891 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(176): Show |
183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1126+554A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94456891 | |||||||
| chr9:94456969 | A | AC | 21 | a0001c0001t0001g0084 a0001c0001t0001g0274 a0001c0001t0001g0276 others(18): Show |
21 | HG00423.hp1 HG00423.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1126+638dupC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94456969 | ||||||
| chr9:94457053 | G | A | 7 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 others(4): Show |
7 | HG00140.hp1 HG01074.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126+716G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457053 | |||||||
| chr9:94457109 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(20): Show |
24 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1126+772C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457109 | |||||||
| chr9:94457213 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1126+876C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457213 | |||||||
| chr9:94457214 | G | A | 8 | a0001c0001t0001g0300 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
8 | HG00408.hp2 HG00438.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126+877G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457214 | |||||||
| chr9:94457396 | CTTTT | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1127-921_1127-918d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94457396 | ||||||
| chr9:94457404 | T | A | 1 | a0001c0001t0003g0177 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1127-918T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457404 | |||||||
| chr9:94457453 | A | AT | 54 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0035 others(51): Show |
55 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1127-859dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94457453 | ||||||
| chr9:94457453 | A | ATT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(119): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1127-860_1127-859d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94457453 | ||||||
| chr9:94457464 | C | G | 11 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1127-858C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457464 | |||||||
| chr9:94457470 | C | T | 1 | a0001c0001t0004g0067 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1127-852C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457470 | |||||||
| chr9:94457631 | C | G | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-691C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457631 | |||||||
| chr9:94457635 | G | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-687G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457635 | |||||||
| chr9:94457636 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-686C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457636 | |||||||
| chr9:94457637 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-685C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457637 | |||||||
| chr9:94457640 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-682G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457640 | |||||||
| chr9:94457641 | G | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-681G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457641 | |||||||
| chr9:94457642 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-680C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457642 | |||||||
| chr9:94457644 | T | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-678T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457644 | |||||||
| chr9:94457645 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-677C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457645 | |||||||
| chr9:94457647 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-675G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457647 | |||||||
| chr9:94457649 | C | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-673C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457649 | |||||||
| chr9:94457650 | A | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-672A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457650 | |||||||
| chr9:94457651 | G | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-671G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457651 | |||||||
| chr9:94457653 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-669C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457653 | |||||||
| chr9:94457655 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-667C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457655 | |||||||
| chr9:94457656 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-666C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457656 | |||||||
| chr9:94457657 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-665G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457657 | |||||||
| chr9:94457659 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-663C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457659 | |||||||
| chr9:94457660 | C | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-662C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457660 | |||||||
| chr9:94457662 | G | T | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-660G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457662 | |||||||
| chr9:94457664 | C | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-658C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457664 | |||||||
| chr9:94457666 | T | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-656T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457666 | |||||||
| chr9:94457676 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-646G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457676 | |||||||
| chr9:94457677 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-645G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457677 | |||||||
| chr9:94457683 | C | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-639C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457683 | |||||||
| chr9:94457685 | T | G | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-637T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457685 | |||||||
| chr9:94457690 | C | A | 1 | a0001c0001t0003g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-632C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457690 | |||||||
| chr9:94457726 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(242): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1127-596G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457726 | |||||||
| chr9:94457759 | G | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.1127-563G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457759 | |||||||
| chr9:94457949 | G | C | 1 | a0001c0001t0002g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1127-373G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457949 | |||||||
| chr9:94458164 | T | G | 2 | a0001c0001t0004g0056 a0001c0001t0004g0064 |
2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1127-158T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94458164 | |||||||
| chr9:94458203 | T | TCTC | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(243): Show |
250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1127-118_1127-116d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94458203 | ||||||
| chr9:94458311 | T | C | 4 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0099 others(1): Show |
4 | HG00099.hp2 HG00280.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127-11T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94458311 | |||||||
| chr9:94458577 | G | C | 10 | a0001c0001t0007g0009 a0001c0001t0007g0010 a0001c0001t0007g0011 others(7): Show |
10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1269+113G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94458577 | |||||||
| chr9:94458611 | G | A | 1 | a0001c0001t0017g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1269+147G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94458611 | |||||||
| chr9:94458664 | T | TA | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(133): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1269+202dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr9 | 94458664 | ||||||
| chr9:94458731 | G | A | 1 | a0001c0001t0003g0247 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1269+267G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94458731 | |||||||
| chr9:94458880 | A | C | 1 | a0001c0001t0006g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1270-281A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94458880 | |||||||
| chr9:94459085 | T | G | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1270-76T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94459085 | |||||||
| chr9:94459152 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0079 others(175): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1270-9G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94459152 |