Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4724 |
| ensemblid | ENSG00000164258.12 |
| hgncid | 7711 |
| symbol | NDUFS4 |
| name | NADH:ubiquinone oxidoreductase subunit S4 |
| refseq_nuc | NM_002495.4 |
| refseq_prot | NP_002486.1 |
| ensembl_nuc | ENST00000296684.10 |
| ensembl_prot | ENSP00000296684.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 53560639 |
| end | 53683338 |
| strand | + |
| ver | v1.2 |
| region | chr5:53560639-53683338 |
| region5000 | chr5:53555639-53688338 |
| regionname0 | NDUFS4_chr5_53560639_53683338 |
| regionname5000 | NDUFS4_chr5_53555639_53688338 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 175 | 375 | 89 | 73 | 161 | 12 | 38 | 136 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | MAAVS others(170): Show |
chr5 | 53555639 | 53688338 |
| a0002 | 0/0 | 175 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | MAAVS others(170): Show |
chr5 | 53555639 | 53688338 |
| a0003 | 0/0 | 175 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | MAALS others(170): Show |
chr5 | 53555639 | 53688338 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 525 | 232 | 68 | 48 | 89 | 6 | 20 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATGGC others(520): Show |
chr5 | 53555639 | 53688338 | ||
| a0001c0002 | 0/0 | 525 | 50 | 13 | 9 | 15 | 3 | 10 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATGGC others(520): Show |
chr5 | 53555639 | 53688338 | ||
| a0001c0003 | 0/0 | 525 | 50 | 4 | 12 | 26 | 3 | 5 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATGGC others(520): Show |
chr5 | 53555639 | 53688338 | ||
| a0001c0004 | 1/0 | 525 | 39 | 1 | 4 | 30 | 0 | 3 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATGGC others(520): Show |
chr5 | 53555639 | 53688338 | ||
| a0001c0007 | 0/0 | 525 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATGGC others(520): Show |
chr5 | 53555639 | 53688338 | ||
| a0001c0008 | 0/0 | 525 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATGGC others(520): Show |
chr5 | 53555639 | 53688338 | ||
| a0001c0009 | 0/0 | 525 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATGGC others(520): Show |
chr5 | 53555639 | 53688338 | ||
| a0001c0010 | 0/0 | 525 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATGGC others(520): Show |
chr5 | 53555639 | 53688338 | ||
| a0002c0005 | 0/0 | 525 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATGGC others(520): Show |
chr5 | 53555639 | 53688338 | ||
| a0003c0006 | 0/0 | 525 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATGGC others(520): Show |
chr5 | 53555639 | 53688338 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 669 | 130 | 39 | 18 | 56 | 3 | 13 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0001t0002 | 0/0 | 669 | 95 | 27 | 30 | 28 | 3 | 7 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0001t0003 | 0/0 | 669 | 4 | 0 | 0 | 4 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATACT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0001t0004 | 0/0 | 669 | 2 | 2 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0001t0005 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0002t0001 | 0/0 | 669 | 50 | 13 | 9 | 15 | 3 | 10 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0003t0001 | 0/0 | 669 | 3 | 3 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0003t0002 | 0/0 | 669 | 47 | 1 | 12 | 26 | 3 | 5 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0004t0001 | 1/0 | 669 | 39 | 1 | 4 | 30 | 0 | 3 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0007t0002 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0008t0001 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0009t0001 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0001c0010t0001 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0002c0005t0002 | 0/0 | 669 | 2 | 1 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| a0003c0006t0002 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | ATCCT others(664): Show |
chr5 | 53555639 | 53688338 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0001t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0022 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0007t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0008t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0009t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0001c0010t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0002c0005t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0002c0005t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| a0003c0006t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0240 | EUR | GBR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0128 | EUR | GBR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | GBR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0101 | EUR | GBR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0064 | EUR | FIN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0203 | EUR | FIN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00438 | hp2 | a0001 | c0004 | t0001 | g0029 | EAS | CHS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00558 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | CHS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0090 | EAS | CHS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | CHS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0368 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0110 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00673 | hp2 | a0001 | c0003 | t0002 | g0136 | EAS | CHS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0104 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0107 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01071 | hp1 | a0001 | c0003 | t0002 | g0140 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01074 | hp2 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0100 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01167 | hp2 | a0001 | c0003 | t0002 | g0103 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0111 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01243 | hp1 | a0002 | c0005 | t0002 | g0159 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0109 | AMR | PUR | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0367 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0120 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0051 | EUR | IBS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0312 | EUR | IBS | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01884 | hp2 | a0001 | c0009 | t0001 | g0274 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01952 | hp1 | a0001 | c0004 | t0001 | g0028 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0106 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02015 | hp1 | a0001 | c0003 | t0002 | g0122 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02027 | hp2 | a0003 | c0006 | t0002 | g0093 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0117 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02040 | hp2 | a0001 | c0008 | t0001 | g0308 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02129 | hp1 | a0001 | c0004 | t0001 | g0031 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0138 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0137 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CDX | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0126 | EAS | CDX | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0011 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0270 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0018 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02698 | hp2 | a0001 | c0003 | t0002 | g0139 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0156 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0158 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0264 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0033 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03195 | hp2 | a0001 | c0010 | t0001 | g0284 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0130 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0348 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0118 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0099 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | BEB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | BEB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | BEB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03927 | hp2 | a0001 | c0003 | t0002 | g0105 | SAS | BEB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0360 | SAS | BEB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0027 | SAS | BEB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | STU | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | STU | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0048 | SAS | BEB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | BEB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | STU | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG04199 | hp2 | a0001 | c0004 | t0001 | g0014 | SAS | STU | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | STU | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | STU | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | STU | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | STU | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | YRI | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | YRI | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18612 | hp1 | a0001 | c0004 | t0001 | g0020 | EAS | CHB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | CHB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18939 | hp1 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0123 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0089 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18946 | hp1 | a0001 | c0004 | t0001 | g0032 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18953 | hp2 | a0001 | c0003 | t0002 | g0135 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0016 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18962 | hp1 | a0001 | c0003 | t0002 | g0131 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18964 | hp1 | a0001 | c0003 | t0002 | g0114 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18968 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0132 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18971 | hp2 | a0001 | c0004 | t0001 | g0017 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18972 | hp1 | a0001 | c0003 | t0002 | g0149 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18972 | hp2 | a0001 | c0004 | t0001 | g0019 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18974 | hp1 | a0001 | c0003 | t0002 | g0228 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18974 | hp2 | a0001 | c0004 | t0001 | g0038 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0085 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18982 | hp2 | a0001 | c0004 | t0001 | g0035 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0026 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18986 | hp1 | a0001 | c0004 | t0001 | g0087 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18987 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18990 | hp2 | a0001 | c0004 | t0001 | g0012 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18993 | hp2 | a0001 | c0003 | t0002 | g0121 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18994 | hp1 | a0001 | c0003 | t0002 | g0134 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0349 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18999 | hp2 | a0001 | c0003 | t0002 | g0115 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19001 | hp2 | a0001 | c0003 | t0002 | g0119 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19003 | hp1 | a0001 | c0003 | t0002 | g0227 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19003 | hp2 | a0001 | c0004 | t0001 | g0023 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0113 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19009 | hp1 | a0001 | c0004 | t0001 | g0030 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19011 | hp1 | a0001 | c0004 | t0001 | g0037 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0129 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19012 | hp2 | a0001 | c0004 | t0001 | g0036 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19030 | hp1 | a0002 | c0005 | t0002 | g0160 | AFR | LWK | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | LWK | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | LWK | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19043 | hp2 | a0001 | c0007 | t0002 | g0178 | AFR | LWK | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19055 | hp2 | a0001 | c0004 | t0001 | g0025 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19057 | hp2 | a0001 | c0003 | t0002 | g0125 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0088 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19066 | hp2 | a0001 | c0004 | t0001 | g0084 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0133 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0091 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19068 | hp2 | a0001 | c0003 | t0002 | g0116 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0141 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19077 | hp2 | a0001 | c0003 | t0002 | g0127 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19080 | hp1 | a0001 | c0003 | t0002 | g0124 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19080 | hp2 | a0001 | c0004 | t0001 | g0039 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19086 | hp2 | a0001 | c0004 | t0001 | g0034 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ASW | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0112 | AFR | ASW | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0061 | EUR | TSI | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0108 | EUR | TSI | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0182 | EUR | TSI | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0309 | EUR | TSI | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | USA | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | USA | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | USA | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | USA | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | LWK | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | LWK | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0094 | REF | REF | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0001 | g0022 | REF | REF | NDUFS4_chr5_53555639_53688338 | NDUFS4 | chr5 | 53555639 | 53688338 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:53560672 | G | C | 1 | a0003 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.10G>C | p.Val4Leu | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/5 | 34/669 | 10/528 | 4/175 | chr5 | 53560672 | |||
| chr5:53560742 | T | A | 1 | a0002 | 2 | HG01243.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.80T>A | p.Val27Asp | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/5 | 104/669 | 80/528 | 27/175 | chr5 | 53560742 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:53560674 | G | C | 7 | a0001c0001 a0001c0007 a0001c0008 others(4): Show |
238 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(235): Show |
synonymous_variant | LOW | c.12G>C | p.Val4Val | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/5 | 36/669 | 12/528 | 4/175 | chr5 | 53560674 | |||
| chr5:53603455 | G | A | 1 | a0001c0007 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.102G>A | p.Ser34Ser | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/5 | 126/669 | 102/528 | 34/175 | chr5 | 53603455 | |||
| chr5:53603521 | T | C | 1 | a0001c0008 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.168T>C | p.Asp56Asp | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/5 | 192/669 | 168/528 | 56/175 | chr5 | 53603521 | |||
| chr5:53646253 | A | C | 9 | a0001c0001 a0001c0002 a0001c0003 others(6): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
synonymous_variant | LOW | c.198A>C | p.Gly66Gly | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/5 | 222/669 | 198/528 | 66/175 | chr5 | 53646253 | |||
| chr5:53646367 | A | G | 7 | a0001c0001 a0001c0003 a0001c0007 others(4): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
synonymous_variant | LOW | c.312A>G | p.Arg104Arg | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/5 | 336/669 | 312/528 | 104/175 | chr5 | 53646367 | |||
| chr5:53683173 | T | C | 1 | a0001c0010 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.480T>C | p.Tyr160Tyr | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 5/5 | 504/669 | 480/528 | 160/175 | chr5 | 53683173 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:53560641 | C | A | 1 | a0001c0001t0003 | 4 | NA18941.hp2 NA18951.hp2 NA18955.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-22C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/5 | 22 | chr5 | 53560641 | ||||||
| chr5:53560657 | A | T | 1 | a0001c0001t0004 | 2 | HG02630.hp1 HG06807.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/5 | chr5 | 53560657 | |||||||
| chr5:53683234 | T | G | 1 | a0001c0001t0005 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 5/5 | 13 | chr5 | 53683234 | ||||||
| chr5:53683267 | G | A | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 others(3): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*46G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 5/5 | 46 | chr5 | 53683267 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:53560790 | C | T | 1 | a0001c0001t0001g0372 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.98+30C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53560790 | |||||||
| chr5:53560886 | A | G | 285 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(282): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.98+126A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53560886 | |||||||
| chr5:53560919 | G | C | 1 | a0003c0006t0002g0093 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.98+159G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53560919 | |||||||
| chr5:53560967 | G | T | 105 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(102): Show |
106 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.98+207G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53560967 | |||||||
| chr5:53561049 | A | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | HG01255.hp2 HG01358.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+289A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53561049 | |||||||
| chr5:53561425 | C | A | 2 | a0001c0002t0001g0007 a0001c0002t0001g0008 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.98+665C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53561425 | |||||||
| chr5:53561513 | AT | A | 365 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(362): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.98+766delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53561513 | ||||||
| chr5:53561760 | T | G | 1 | a0001c0001t0002g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.98+1000T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53561760 | |||||||
| chr5:53561890 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.98+1130C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53561890 | |||||||
| chr5:53561951 | C | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.98+1191C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53561951 | |||||||
| chr5:53561961 | T | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.98+1201T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53561961 | |||||||
| chr5:53561991 | AT | A | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | HG00423.hp1 HG00558.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.98+1236delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53561991 | ||||||
| chr5:53562034 | C | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.98+1274C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53562034 | |||||||
| chr5:53562073 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+1313G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53562073 | |||||||
| chr5:53562194 | G | A | 1 | a0001c0004t0001g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.98+1434G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53562194 | |||||||
| chr5:53562301 | C | T | 3 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 |
3 | HG01081.hp1 HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.98+1541C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53562301 | |||||||
| chr5:53562528 | C | A | 2 | a0001c0003t0002g0099 a0001c0003t0002g0100 |
2 | HG01099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.98+1768C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53562528 | |||||||
| chr5:53562542 | A | G | 1 | a0001c0001t0001g0371 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.98+1782A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53562542 | |||||||
| chr5:53562569 | G | A | 1 | a0001c0003t0002g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.98+1809G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53562569 | |||||||
| chr5:53562707 | A | C | 1 | a0001c0002t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.98+1947A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53562707 | |||||||
| chr5:53562817 | C | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.98+2057C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53562817 | |||||||
| chr5:53563066 | A | T | 82 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
86 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.98+2306A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563066 | |||||||
| chr5:53563089 | C | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.98+2329C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563089 | |||||||
| chr5:53563102 | G | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.98+2342G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563102 | |||||||
| chr5:53563146 | G | A | 13 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG01109.hp1 HG01433.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.98+2386G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563146 | |||||||
| chr5:53563183 | C | T | 2 | a0001c0001t0001g0369 a0001c0001t0001g0370 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.98+2423C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563183 | |||||||
| chr5:53563236 | C | CA | 57 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(54): Show |
58 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.98+2494dupA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53563236 | ||||||
| chr5:53563236 | C | CAA | 19 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(16): Show |
19 | HG00140.hp1 HG01106.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.98+2493_98+2494dup others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53563236 | ||||||
| chr5:53563308 | A | G | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.98+2548A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563308 | |||||||
| chr5:53563320 | A | G | 1 | a0001c0001t0001g0371 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.98+2560A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563320 | |||||||
| chr5:53563434 | A | G | 1 | a0001c0004t0001g0091 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.98+2674A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563434 | |||||||
| chr5:53563503 | AT | A | 44 | a0001c0001t0001g0275 a0001c0003t0002g0001 a0001c0003t0002g0099 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.98+2757delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53563503 | ||||||
| chr5:53563595 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+2835G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563595 | |||||||
| chr5:53563654 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.98+2894A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563654 | |||||||
| chr5:53563753 | C | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.98+2993C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563753 | |||||||
| chr5:53563782 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.98+3022G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563782 | |||||||
| chr5:53563794 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.98+3034G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563794 | |||||||
| chr5:53563946 | G | A | 1 | a0001c0007t0002g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.98+3186G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53563946 | |||||||
| chr5:53564103 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.98+3343T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53564103 | |||||||
| chr5:53564137 | T | C | 1 | a0001c0003t0002g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.98+3377T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53564137 | |||||||
| chr5:53564159 | C | T | 4 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(1): Show |
4 | NA18942.hp1 NA18951.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+3399C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53564159 | |||||||
| chr5:53564386 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.98+3626A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53564386 | |||||||
| chr5:53564611 | C | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.98+3851C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53564611 | |||||||
| chr5:53564752 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+3992A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53564752 | |||||||
| chr5:53564883 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.98+4123A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53564883 | |||||||
| chr5:53564887 | A | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.98+4127A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53564887 | |||||||
| chr5:53565097 | G | A | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.98+4337G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53565097 | |||||||
| chr5:53565122 | T | C | 1 | a0001c0004t0001g0011 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.98+4362T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53565122 | |||||||
| chr5:53565266 | A | G | 1 | a0001c0002t0001g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.98+4506A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53565266 | |||||||
| chr5:53565397 | T | C | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG01975.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.98+4637T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53565397 | |||||||
| chr5:53565696 | CTG | C | 8 | a0001c0004t0001g0084 a0001c0004t0001g0085 a0001c0004t0001g0086 others(5): Show |
8 | HG00609.hp1 NA18944.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.98+4938_98+4939del others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53565696 | ||||||
| chr5:53565759 | G | A | 7 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(4): Show |
7 | HG01496.hp1 HG01928.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+4999G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53565759 | |||||||
| chr5:53565864 | A | C | 2 | a0001c0001t0001g0367 a0001c0001t0001g0368 |
2 | HG00639.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.98+5104A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53565864 | |||||||
| chr5:53565869 | A | G | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.98+5109A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53565869 | |||||||
| chr5:53565875 | TAA | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.98+5119_98+5120del others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53565875 | ||||||
| chr5:53565944 | C | T | 6 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG02723.hp2 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+5184C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53565944 | |||||||
| chr5:53565970 | G | A | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.98+5210G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53565970 | |||||||
| chr5:53565997 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.98+5237C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53565997 | |||||||
| chr5:53566073 | C | T | 3 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0245 |
3 | NA18959.hp1 NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.98+5313C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53566073 | |||||||
| chr5:53566128 | G | T | 2 | a0002c0005t0002g0159 a0002c0005t0002g0160 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98+5368G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53566128 | |||||||
| chr5:53566138 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.98+5378A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53566138 | |||||||
| chr5:53566544 | G | T | 332 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(329): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.98+5784G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53566544 | |||||||
| chr5:53566579 | G | C | 143 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(140): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.98+5819G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53566579 | |||||||
| chr5:53566637 | C | A | 1 | a0001c0004t0001g0012 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.98+5877C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53566637 | |||||||
| chr5:53566825 | G | A | 6 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0211 others(3): Show |
6 | NA18952.hp1 NA18973.hp2 NA19055.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+6065G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53566825 | |||||||
| chr5:53566849 | A | AT | 107 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(104): Show |
108 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.98+6106dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53566849 | ||||||
| chr5:53566849 | A | ATT | 14 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(11): Show |
14 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.98+6105_98+6106dup others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53566849 | ||||||
| chr5:53566923 | A | G | 1 | a0001c0004t0001g0039 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.98+6163A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53566923 | |||||||
| chr5:53566953 | A | G | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0009t0001g0274 |
3 | HG01884.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.98+6193A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53566953 | |||||||
| chr5:53566995 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.98+6235C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53566995 | |||||||
| chr5:53567039 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG01167.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.98+6279C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53567039 | |||||||
| chr5:53567061 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.98+6301G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53567061 | |||||||
| chr5:53567128 | C | A | 1 | a0001c0003t0001g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.98+6368C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53567128 | |||||||
| chr5:53567128 | C | T | 65 | a0001c0001t0001g0006 a0001c0001t0001g0288 a0001c0001t0001g0289 others(62): Show |
66 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.98+6368C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53567128 | |||||||
| chr5:53567423 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.98+6663A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53567423 | |||||||
| chr5:53567666 | G | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(88): Show |
92 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.98+6906G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53567666 | |||||||
| chr5:53567666 | G | T | 2 | a0001c0002t0001g0161 a0001c0003t0001g0156 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.98+6906G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53567666 | |||||||
| chr5:53567808 | A | T | 285 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(282): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.98+7048A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53567808 | |||||||
| chr5:53567910 | C | A | 18 | a0001c0003t0002g0001 a0001c0003t0002g0099 a0001c0003t0002g0100 others(15): Show |
19 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.98+7150C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53567910 | |||||||
| chr5:53567984 | A | T | 6 | a0001c0004t0001g0012 a0001c0004t0001g0034 a0001c0004t0001g0035 others(3): Show |
6 | NA18974.hp2 NA18982.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.98+7224A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53567984 | |||||||
| chr5:53568033 | T | C | 2 | a0002c0005t0002g0159 a0002c0005t0002g0160 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98+7273T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568033 | |||||||
| chr5:53568183 | C | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0009t0001g0274 |
3 | HG01884.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.98+7423C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568183 | |||||||
| chr5:53568226 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+7466C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568226 | |||||||
| chr5:53568268 | T | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.98+7508T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568268 | |||||||
| chr5:53568269 | T | C | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.98+7509T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568269 | |||||||
| chr5:53568310 | A | T | 53 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(50): Show |
56 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.98+7550A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568310 | |||||||
| chr5:53568380 | G | T | 1 | a0001c0001t0001g0313 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.98+7620G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568380 | |||||||
| chr5:53568476 | C | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+7716C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568476 | |||||||
| chr5:53568535 | A | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.98+7775A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568535 | |||||||
| chr5:53568553 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+7793G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568553 | |||||||
| chr5:53568597 | G | A | 2 | a0001c0004t0001g0013 a0001c0004t0001g0014 |
2 | HG01074.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.98+7837G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568597 | |||||||
| chr5:53568637 | T | C | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.98+7877T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568637 | |||||||
| chr5:53568706 | A | G | 1 | a0001c0001t0001g0364 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.98+7946A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568706 | |||||||
| chr5:53568883 | T | A | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.98+8123T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568883 | |||||||
| chr5:53568965 | T | C | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.98+8205T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568965 | |||||||
| chr5:53568972 | A | T | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.98+8212A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53568972 | |||||||
| chr5:53569346 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.98+8586A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53569346 | |||||||
| chr5:53569653 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.98+8893G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53569653 | |||||||
| chr5:53569811 | C | T | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.98+9051C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53569811 | |||||||
| chr5:53570204 | A | C | 4 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0363 others(1): Show |
4 | HG00609.hp2 NA18990.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+9444A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53570204 | |||||||
| chr5:53570270 | G | A | 146 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.98+9510G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53570270 | |||||||
| chr5:53570279 | T | C | 2 | a0001c0002t0001g0161 a0001c0003t0001g0156 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.98+9519T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53570279 | |||||||
| chr5:53570316 | G | A | 262 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.98+9556G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53570316 | |||||||
| chr5:53570630 | T | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.98+9870T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53570630 | |||||||
| chr5:53570684 | C | CT | 103 | a0001c0001t0001g0006 a0001c0001t0001g0261 a0001c0001t0001g0275 others(100): Show |
104 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.98+9941dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53570684 | ||||||
| chr5:53570684 | CT | C | 91 | a0001c0001t0002g0002 a0001c0001t0002g0095 a0001c0001t0002g0102 others(88): Show |
93 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.98+9941delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53570684 | ||||||
| chr5:53570872 | C | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0009t0001g0274 |
3 | HG01884.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.98+10112C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53570872 | |||||||
| chr5:53570979 | C | T | 1 | a0001c0001t0001g0363 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.98+10219C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53570979 | |||||||
| chr5:53571010 | A | G | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0009t0001g0274 |
3 | HG01884.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.98+10250A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571010 | |||||||
| chr5:53571033 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.98+10273C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571033 | |||||||
| chr5:53571039 | T | A | 1 | a0001c0003t0002g0103 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.98+10279T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571039 | |||||||
| chr5:53571066 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+10306A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571066 | |||||||
| chr5:53571200 | C | T | 1 | a0001c0009t0001g0274 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.98+10440C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571200 | |||||||
| chr5:53571209 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.98+10449C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571209 | |||||||
| chr5:53571460 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.98+10700T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571460 | |||||||
| chr5:53571500 | T | G | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.98+10740T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571500 | |||||||
| chr5:53571558 | A | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.98+10798A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571558 | |||||||
| chr5:53571652 | A | G | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.98+10892A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571652 | |||||||
| chr5:53571875 | T | G | 3 | a0001c0003t0002g0101 a0001c0003t0002g0104 a0001c0003t0002g0105 |
3 | HG00140.hp2 HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.98+11115T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53571875 | |||||||
| chr5:53572111 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.98+11351G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572111 | |||||||
| chr5:53572156 | G | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.98+11396G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572156 | |||||||
| chr5:53572315 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+11555C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572315 | |||||||
| chr5:53572383 | C | T | 2 | a0001c0002t0001g0007 a0001c0002t0001g0008 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.98+11623C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572383 | |||||||
| chr5:53572403 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.98+11643A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572403 | |||||||
| chr5:53572617 | G | A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+11857G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572617 | |||||||
| chr5:53572649 | G | GT | 11 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0002t0001g0081 others(8): Show |
11 | HG00673.hp2 HG01256.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+11903dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53572649 | ||||||
| chr5:53572666 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.98+11906C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572666 | |||||||
| chr5:53572674 | C | T | 1 | a0001c0003t0002g0116 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.98+11914C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572674 | |||||||
| chr5:53572678 | C | G | 1 | a0001c0001t0001g0313 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.98+11918C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572678 | |||||||
| chr5:53572847 | T | C | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.98+12087T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572847 | |||||||
| chr5:53572950 | GTTTTTTG others(6): Show |
G | 3 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0080 |
3 | HG02717.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.98+12210_98+12222d others(15): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53572950 | ||||||
| chr5:53572956 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+12196T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572956 | |||||||
| chr5:53572957 | GTTTTTTT others(7): Show |
G | 1 | a0001c0003t0002g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.98+12210_98+12223d others(16): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53572957 | ||||||
| chr5:53572969 | TG | T | 62 | a0001c0001t0001g0142 a0001c0001t0001g0164 a0001c0001t0001g0165 others(59): Show |
63 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.98+12210delG | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572969 | |||||||
| chr5:53572970 | G | GT | 7 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0043 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+12225dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53572970 | ||||||
| chr5:53572970 | G | T | 11 | a0001c0001t0001g0169 a0001c0001t0002g0193 a0001c0001t0002g0207 others(8): Show |
11 | HG00558.hp1 HG01109.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+12210G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572970 | |||||||
| chr5:53572970 | GT | G | 99 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0095 others(96): Show |
102 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.98+12225delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53572970 | ||||||
| chr5:53572970 | GTT | G | 101 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(98): Show |
102 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.98+12224_98+12225d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53572970 | ||||||
| chr5:53572971 | T | G | 2 | a0001c0001t0001g0169 a0001c0001t0002g0242 |
2 | HG03831.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.98+12211T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572971 | |||||||
| chr5:53572972 | T | G | 34 | a0001c0001t0001g0142 a0001c0001t0001g0164 a0001c0001t0001g0165 others(31): Show |
34 | HG00140.hp1 HG01099.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.98+12212T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572972 | |||||||
| chr5:53572977 | T | G | 1 | a0001c0004t0001g0015 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.98+12217T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53572977 | |||||||
| chr5:53573050 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.98+12290G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53573050 | |||||||
| chr5:53573159 | A | G | 1 | a0001c0004t0001g0033 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.98+12399A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53573159 | |||||||
| chr5:53573175 | G | A | 132 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(129): Show |
133 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.98+12415G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53573175 | |||||||
| chr5:53573342 | A | T | 133 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(130): Show |
134 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.98+12582A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53573342 | |||||||
| chr5:53573493 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+12733C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53573493 | |||||||
| chr5:53573509 | A | G | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.98+12749A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53573509 | |||||||
| chr5:53573554 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.98+12794G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53573554 | |||||||
| chr5:53573638 | G | T | 1 | a0001c0002t0001g0079 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.98+12878G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53573638 | |||||||
| chr5:53573723 | C | T | 37 | a0001c0002t0001g0040 a0001c0002t0001g0047 a0001c0002t0001g0048 others(34): Show |
37 | HG00323.hp1 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.98+12963C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53573723 | |||||||
| chr5:53573841 | C | T | 105 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(102): Show |
106 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.98+13081C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53573841 | |||||||
| chr5:53574012 | G | A | 3 | a0001c0002t0001g0157 a0001c0002t0001g0163 a0001c0003t0001g0158 |
3 | HG02451.hp1 HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.98+13252G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53574012 | |||||||
| chr5:53574111 | A | G | 1 | a0001c0001t0001g0360 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.98+13351A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53574111 | |||||||
| chr5:53574152 | T | C | 2 | a0001c0002t0001g0161 a0001c0003t0001g0156 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.98+13392T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53574152 | |||||||
| chr5:53574154 | T | C | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.98+13394T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53574154 | |||||||
| chr5:53574420 | T | A | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.98+13660T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53574420 | |||||||
| chr5:53574488 | A | G | 2 | a0002c0005t0002g0159 a0002c0005t0002g0160 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98+13728A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53574488 | |||||||
| chr5:53574634 | A | G | 1 | a0001c0002t0001g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.98+13874A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53574634 | |||||||
| chr5:53574646 | A | T | 285 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(282): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.98+13886A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53574646 | |||||||
| chr5:53574843 | GA | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.98+14087delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53574843 | ||||||
| chr5:53574939 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.98+14179G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53574939 | |||||||
| chr5:53575130 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.98+14370G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53575130 | |||||||
| chr5:53575155 | G | A | 1 | a0001c0001t0003g0217 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.98+14395G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53575155 | |||||||
| chr5:53575291 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.98+14531G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53575291 | |||||||
| chr5:53575447 | G | A | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.98+14687G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53575447 | |||||||
| chr5:53575530 | C | CT | 24 | a0001c0001t0001g0142 a0001c0001t0002g0250 a0001c0002t0001g0043 others(21): Show |
24 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.98+14798dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53575530 | ||||||
| chr5:53575530 | CT | C | 19 | a0001c0001t0002g0185 a0001c0001t0002g0214 a0001c0001t0002g0235 others(16): Show |
19 | HG00099.hp1 HG00733.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.98+14798delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53575530 | ||||||
| chr5:53575530 | CTT | C | 54 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0095 others(51): Show |
57 | HG00423.hp1 HG00558.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.98+14797_98+14798d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53575530 | ||||||
| chr5:53575530 | CTTT | C | 85 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0001g0286 others(82): Show |
87 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.98+14796_98+14798d others(5): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53575530 | ||||||
| chr5:53575530 | CTTTT | C | 95 | a0001c0001t0001g0006 a0001c0001t0001g0169 a0001c0001t0001g0172 others(92): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.98+14795_98+14798d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53575530 | ||||||
| chr5:53575530 | CTTTTT | C | 29 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(26): Show |
29 | HG01099.hp1 HG01169.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.98+14794_98+14798d others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53575530 | ||||||
| chr5:53575530 | CTTTTTTT others(5): Show |
C | 7 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0049 others(4): Show |
7 | HG00741.hp1 HG01123.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+14787_98+14798d others(14): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53575530 | ||||||
| chr5:53575584 | T | C | 133 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(130): Show |
134 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.98+14824T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53575584 | |||||||
| chr5:53575634 | C | T | 102 | a0001c0001t0001g0006 a0001c0001t0001g0272 a0001c0001t0001g0273 others(99): Show |
103 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.98+14874C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53575634 | |||||||
| chr5:53575666 | C | T | 4 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(1): Show |
4 | NA18939.hp2 NA18955.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+14906C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53575666 | |||||||
| chr5:53575678 | AT | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.98+14920delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53575678 | ||||||
| chr5:53575748 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.98+14988G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53575748 | |||||||
| chr5:53575837 | T | G | 1 | a0001c0003t0002g0117 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.98+15077T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53575837 | |||||||
| chr5:53576034 | C | A | 82 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
86 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.98+15274C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53576034 | |||||||
| chr5:53576102 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.98+15342A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53576102 | |||||||
| chr5:53576167 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG01167.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.98+15407G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53576167 | |||||||
| chr5:53576286 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.98+15526A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53576286 | |||||||
| chr5:53576317 | GAA | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.98+15558_98+15559d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53576317 | |||||||
| chr5:53576603 | G | C | 1 | a0001c0001t0002g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.98+15843G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53576603 | |||||||
| chr5:53576637 | ACT | A | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.98+15879_98+15880d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53576637 | ||||||
| chr5:53576676 | T | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.98+15916T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53576676 | |||||||
| chr5:53576740 | A | G | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.98+15980A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53576740 | |||||||
| chr5:53576941 | C | G | 1 | a0001c0002t0001g0008 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.98+16181C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53576941 | |||||||
| chr5:53576962 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.98+16202G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53576962 | |||||||
| chr5:53577327 | G | A | 22 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0208 others(19): Show |
25 | HG01928.hp2 HG01934.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.98+16567G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53577327 | |||||||
| chr5:53577413 | G | C | 2 | a0001c0003t0002g0099 a0001c0003t0002g0100 |
2 | HG01099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.98+16653G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53577413 | |||||||
| chr5:53577461 | A | G | 4 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 others(1): Show |
4 | NA18942.hp2 NA18965.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+16701A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53577461 | |||||||
| chr5:53577472 | A | G | 2 | a0001c0001t0002g0152 a0001c0001t0002g0154 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.98+16712A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53577472 | |||||||
| chr5:53577482 | AT | A | 309 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.98+16736delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53577482 | ||||||
| chr5:53577482 | ATT | A | 18 | a0001c0001t0001g0142 a0001c0001t0001g0251 a0001c0001t0001g0252 others(15): Show |
18 | HG00140.hp1 HG01099.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.98+16735_98+16736d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53577482 | ||||||
| chr5:53577609 | C | T | 3 | a0001c0001t0003g0005 a0001c0001t0003g0217 a0001c0001t0003g0237 |
4 | NA18941.hp2 NA18951.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+16849C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53577609 | |||||||
| chr5:53577683 | A | T | 1 | a0001c0003t0002g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.98+16923A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53577683 | |||||||
| chr5:53577747 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.98+16987A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53577747 | |||||||
| chr5:53577946 | G | A | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.98+17186G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53577946 | |||||||
| chr5:53578018 | T | G | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.98+17258T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578018 | |||||||
| chr5:53578070 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0350 a0001c0001t0001g0351 |
4 | NA18966.hp1 NA18980.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+17310C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578070 | |||||||
| chr5:53578121 | G | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.98+17361G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578121 | |||||||
| chr5:53578256 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.98+17496G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578256 | |||||||
| chr5:53578321 | G | C | 13 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG01109.hp1 HG01433.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.98+17561G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578321 | |||||||
| chr5:53578423 | C | T | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.98+17663C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578423 | |||||||
| chr5:53578677 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.98+17917A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578677 | |||||||
| chr5:53578683 | G | A | 1 | a0001c0008t0001g0308 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.98+17923G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578683 | |||||||
| chr5:53578915 | A | G | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.98+18155A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578915 | |||||||
| chr5:53578921 | A | G | 1 | a0001c0001t0001g0361 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.98+18161A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578921 | |||||||
| chr5:53578966 | C | T | 1 | a0001c0004t0001g0026 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.98+18206C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53578966 | |||||||
| chr5:53579008 | C | T | 2 | a0001c0002t0001g0007 a0001c0002t0001g0008 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.98+18248C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53579008 | |||||||
| chr5:53579135 | T | G | 1 | a0001c0001t0001g0362 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.98+18375T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53579135 | |||||||
| chr5:53579166 | C | T | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+18406C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53579166 | |||||||
| chr5:53579175 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98+18415T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53579175 | |||||||
| chr5:53579190 | A | AT | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.98+18432dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53579190 | ||||||
| chr5:53579253 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.98+18493C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53579253 | |||||||
| chr5:53579668 | A | G | 1 | a0001c0001t0005g0349 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.98+18908A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53579668 | |||||||
| chr5:53579673 | G | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.98+18913G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53579673 | |||||||
| chr5:53579763 | G | C | 1 | a0001c0002t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.98+19003G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53579763 | |||||||
| chr5:53579789 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.98+19029G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53579789 | |||||||
| chr5:53579819 | T | C | 6 | a0001c0001t0001g0142 a0001c0002t0001g0157 a0001c0002t0001g0161 others(3): Show |
6 | HG01167.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+19059T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53579819 | |||||||
| chr5:53580029 | T | A | 280 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.98+19269T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580029 | |||||||
| chr5:53580367 | C | T | 1 | a0001c0003t0002g0131 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.98+19607C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580367 | |||||||
| chr5:53580457 | G | A | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0009t0001g0274 |
3 | HG01884.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.98+19697G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580457 | |||||||
| chr5:53580478 | T | C | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.98+19718T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580478 | |||||||
| chr5:53580593 | A | G | 28 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(25): Show |
28 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.98+19833A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580593 | |||||||
| chr5:53580612 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.98+19852G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580612 | |||||||
| chr5:53580665 | CTCTT | C | 60 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(57): Show |
61 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.98+19917_98+19920d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53580665 | ||||||
| chr5:53580686 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.98+19926G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580686 | |||||||
| chr5:53580689 | C | CTTCCT | 3 | a0001c0001t0002g0151 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG03130.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.98+19952_98+19956d others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53580689 | ||||||
| chr5:53580689 | C | CTTCTT | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+19932_98+19933i others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53580689 | ||||||
| chr5:53580693 | C | T | 6 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG02723.hp2 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+19933C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580693 | |||||||
| chr5:53580703 | CTTTCCTT others(4): Show |
C | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.98+19952_98+19962d others(13): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53580703 | ||||||
| chr5:53580708 | CTTTCCT | C | 103 | a0001c0001t0001g0006 a0001c0001t0001g0272 a0001c0001t0001g0273 others(100): Show |
104 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.98+19966_98+19971d others(8): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53580708 | ||||||
| chr5:53580708 | CTTTCCTT others(5): Show |
C | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.98+19960_98+19971d others(14): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53580708 | ||||||
| chr5:53580712 | C | A | 1 | a0001c0007t0002g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.98+19952C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580712 | |||||||
| chr5:53580717 | T | C | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.98+19957T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580717 | |||||||
| chr5:53580733 | T | A | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.98+19973T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580733 | |||||||
| chr5:53580753 | TTCTC | T | 10 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(7): Show |
10 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.98+19995_98+19998d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53580753 | ||||||
| chr5:53580754 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.98+19994T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580754 | |||||||
| chr5:53580755 | CTCTT | C | 3 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0325 |
3 | HG02723.hp1 HG03831.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.98+20011_98+20014d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53580755 | ||||||
| chr5:53580757 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.98+19997C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580757 | |||||||
| chr5:53580994 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.98+20234C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53580994 | |||||||
| chr5:53581022 | G | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.98+20262G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53581022 | |||||||
| chr5:53581932 | C | T | 6 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG02723.hp2 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+21172C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53581932 | |||||||
| chr5:53581936 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.98+21176G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53581936 | |||||||
| chr5:53582027 | C | T | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.98+21267C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582027 | |||||||
| chr5:53582210 | C | CAAAAT | 9 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0002g0189 others(6): Show |
9 | HG00642.hp2 HG00673.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-21211_99-21207d others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53582210 | ||||||
| chr5:53582210 | C | CAAAATAA others(3): Show |
50 | a0001c0001t0002g0102 a0001c0001t0002g0143 a0001c0001t0002g0144 others(47): Show |
51 | HG00140.hp2 HG00642.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.99-21216_99-21207d others(12): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53582210 | ||||||
| chr5:53582210 | C | CAAAATAA others(8): Show |
3 | a0001c0001t0002g0095 a0001c0003t0002g0106 a0001c0003t0002g0107 |
3 | HG01069.hp1 HG01978.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.99-21221_99-21207d others(17): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53582210 | ||||||
| chr5:53582210 | CAAAAT | C | 5 | a0001c0003t0002g0112 a0001c0003t0002g0113 a0001c0003t0002g0114 others(2): Show |
5 | NA18964.hp1 NA18999.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-21211_99-21207d others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53582210 | ||||||
| chr5:53582231 | A | AAAATT | 16 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(13): Show |
16 | HG00140.hp1 HG01169.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.99-21217_99-21216i others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53582231 | ||||||
| chr5:53582231 | A | T | 1 | a0001c0001t0001g0263 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.99-21221A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582231 | |||||||
| chr5:53582236 | A | AAAATT | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.99-21212_99-21211i others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53582236 | ||||||
| chr5:53582236 | A | T | 18 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(15): Show |
18 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.99-21216A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582236 | |||||||
| chr5:53582241 | A | AAAATAAA others(3): Show |
6 | a0001c0001t0002g0150 a0001c0001t0002g0249 a0001c0001t0002g0250 others(3): Show |
6 | HG00099.hp2 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-21207_99-21206i others(12): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53582241 | ||||||
| chr5:53582241 | A | AAAATAAA others(8): Show |
2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99-21207_99-21206i others(17): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53582241 | ||||||
| chr5:53582241 | A | AAAATT | 157 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0275 others(154): Show |
162 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.99-21202_99-21198d others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53582241 | ||||||
| chr5:53582241 | A | T | 36 | a0001c0001t0001g0142 a0001c0001t0001g0251 a0001c0001t0001g0252 others(33): Show |
36 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.99-21211A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582241 | |||||||
| chr5:53582241 | AAAATT | A | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.99-21202_99-21198d others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53582241 | ||||||
| chr5:53582246 | T | A | 5 | a0001c0001t0002g0095 a0001c0003t0002g0106 a0001c0003t0002g0107 others(2): Show |
5 | HG01069.hp1 HG01978.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-21206T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582246 | |||||||
| chr5:53582255 | A | T | 32 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(29): Show |
33 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.99-21197A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582255 | |||||||
| chr5:53582342 | A | C | 44 | a0001c0003t0002g0001 a0001c0003t0002g0099 a0001c0003t0002g0100 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.99-21110A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582342 | |||||||
| chr5:53582390 | C | T | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.99-21062C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582390 | |||||||
| chr5:53582438 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0348 |
2 | HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.99-21014C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582438 | |||||||
| chr5:53582450 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.99-21002C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582450 | |||||||
| chr5:53582451 | C | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.99-21001C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582451 | |||||||
| chr5:53582551 | T | C | 2 | a0001c0002t0001g0055 a0001c0002t0001g0073 |
2 | NA18991.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.99-20901T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582551 | |||||||
| chr5:53582554 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.99-20898G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582554 | |||||||
| chr5:53582704 | C | T | 1 | a0001c0009t0001g0274 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.99-20748C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582704 | |||||||
| chr5:53582759 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.99-20693T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582759 | |||||||
| chr5:53582767 | T | C | 6 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG02723.hp2 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-20685T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582767 | |||||||
| chr5:53582933 | G | A | 1 | a0001c0004t0001g0011 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.99-20519G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582933 | |||||||
| chr5:53582935 | T | C | 7 | a0001c0001t0002g0216 a0001c0001t0002g0218 a0001c0001t0002g0219 others(4): Show |
7 | HG01928.hp2 HG01934.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.99-20517T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582935 | |||||||
| chr5:53582971 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-20481G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53582971 | |||||||
| chr5:53583098 | C | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99-20354C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53583098 | |||||||
| chr5:53583211 | G | A | 1 | a0001c0003t0002g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99-20241G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53583211 | |||||||
| chr5:53583218 | A | G | 1 | a0001c0003t0002g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.99-20234A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53583218 | |||||||
| chr5:53583329 | C | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0254 a0001c0001t0001g0255 |
3 | HG00140.hp1 HG01169.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.99-20123C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53583329 | |||||||
| chr5:53583489 | T | C | 32 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(29): Show |
33 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.99-19963T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53583489 | |||||||
| chr5:53583492 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99-19960A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53583492 | |||||||
| chr5:53583551 | G | T | 147 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.99-19901G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53583551 | |||||||
| chr5:53583641 | T | C | 1 | a0001c0001t0001g0317 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.99-19811T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53583641 | |||||||
| chr5:53583875 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-19577A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53583875 | |||||||
| chr5:53583973 | A | G | 286 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(283): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.99-19479A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53583973 | |||||||
| chr5:53584034 | C | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.99-19418C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584034 | |||||||
| chr5:53584060 | C | G | 1 | a0001c0001t0002g0236 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.99-19392C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584060 | |||||||
| chr5:53584118 | C | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0009t0001g0274 |
3 | HG01884.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99-19334C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584118 | |||||||
| chr5:53584308 | G | A | 44 | a0001c0003t0002g0001 a0001c0003t0002g0099 a0001c0003t0002g0100 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.99-19144G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584308 | |||||||
| chr5:53584345 | G | A | 280 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.99-19107G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584345 | |||||||
| chr5:53584396 | C | G | 3 | a0001c0001t0001g0142 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG01167.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.99-19056C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584396 | |||||||
| chr5:53584415 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.99-19037G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584415 | |||||||
| chr5:53584566 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.99-18886C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584566 | |||||||
| chr5:53584586 | T | A | 2 | a0001c0003t0002g0108 a0001c0003t0002g0109 |
2 | HG01243.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.99-18866T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584586 | |||||||
| chr5:53584769 | C | CTGTTTT | 120 | a0001c0001t0001g0142 a0001c0001t0001g0164 a0001c0001t0001g0165 others(117): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.99-18670_99-18665d others(8): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53584769 | ||||||
| chr5:53584772 | T | TTTTTGG | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.99-18675_99-18674i others(8): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53584772 | ||||||
| chr5:53584857 | T | C | 1 | a0001c0002t0001g0042 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99-18595T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584857 | |||||||
| chr5:53584916 | C | G | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG02109.hp2 HG02257.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-18536C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584916 | |||||||
| chr5:53584917 | G | A | 1 | a0001c0001t0002g0241 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.99-18535G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584917 | |||||||
| chr5:53584917 | G | T | 2 | a0001c0002t0001g0052 a0001c0002t0001g0053 |
2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.99-18535G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53584917 | |||||||
| chr5:53585112 | G | A | 32 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(29): Show |
33 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.99-18340G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585112 | |||||||
| chr5:53585335 | C | T | 1 | a0001c0001t0002g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99-18117C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585335 | |||||||
| chr5:53585352 | A | C | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0002t0001g0071 |
3 | HG03017.hp2 HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.99-18100A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585352 | |||||||
| chr5:53585463 | G | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99-17989G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585463 | |||||||
| chr5:53585468 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99-17984G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585468 | |||||||
| chr5:53585551 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99-17901G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585551 | |||||||
| chr5:53585648 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.99-17804A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585648 | |||||||
| chr5:53585679 | T | G | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.99-17773T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585679 | |||||||
| chr5:53585730 | G | A | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.99-17722G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585730 | |||||||
| chr5:53585745 | A | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(102): Show |
106 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.99-17707A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585745 | |||||||
| chr5:53585753 | AAAAG | A | 13 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(10): Show |
13 | HG02109.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.99-17695_99-17692d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53585753 | ||||||
| chr5:53585836 | T | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.99-17616T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585836 | |||||||
| chr5:53585861 | T | C | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.99-17591T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53585861 | |||||||
| chr5:53586114 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99-17338A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586114 | |||||||
| chr5:53586142 | A | G | 2 | a0001c0002t0001g0007 a0001c0002t0001g0008 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.99-17310A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586142 | |||||||
| chr5:53586161 | T | A | 1 | a0001c0001t0002g0180 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.99-17291T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586161 | |||||||
| chr5:53586169 | A | G | 1 | a0001c0003t0002g0115 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.99-17283A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586169 | |||||||
| chr5:53586279 | A | C | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.99-17173A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586279 | |||||||
| chr5:53586280 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.99-17172G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586280 | |||||||
| chr5:53586329 | C | CA | 61 | a0001c0001t0001g0298 a0001c0001t0001g0318 a0001c0001t0002g0003 others(58): Show |
64 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.99-17107dupA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53586329 | ||||||
| chr5:53586350 | C | A | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.99-17102C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586350 | |||||||
| chr5:53586496 | TTTAG | T | 66 | a0001c0001t0001g0271 a0001c0001t0001g0273 a0001c0001t0002g0003 others(63): Show |
69 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.99-16941_99-16938d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53586496 | ||||||
| chr5:53586496 | TTTAGTTA others(5): Show |
T | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.99-16949_99-16938d others(14): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53586496 | ||||||
| chr5:53586507 | AGTTAGTT others(1): Show |
A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.99-16941_99-16934d others(10): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53586507 | ||||||
| chr5:53586511 | A | T | 3 | a0001c0001t0001g0142 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG01167.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.99-16941A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586511 | |||||||
| chr5:53586515 | T | A | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.99-16937T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586515 | |||||||
| chr5:53586640 | A | T | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.99-16812A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586640 | |||||||
| chr5:53586667 | C | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99-16785C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586667 | |||||||
| chr5:53586668 | G | A | 143 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(140): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.99-16784G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586668 | |||||||
| chr5:53586758 | T | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(133): Show |
137 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.99-16694T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586758 | |||||||
| chr5:53586861 | T | TCACTGAG others(15): Show |
1 | a0001c0004t0001g0016 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.99-16587_99-16566d others(24): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53586861 | ||||||
| chr5:53586905 | C | T | 143 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(140): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.99-16547C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586905 | |||||||
| chr5:53586959 | G | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.99-16493G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53586959 | |||||||
| chr5:53587044 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.99-16408G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587044 | |||||||
| chr5:53587123 | C | T | 82 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
86 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.99-16329C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587123 | |||||||
| chr5:53587240 | G | T | 44 | a0001c0003t0002g0001 a0001c0003t0002g0099 a0001c0003t0002g0100 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.99-16212G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587240 | |||||||
| chr5:53587481 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99-15971A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587481 | |||||||
| chr5:53587485 | T | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.99-15967T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587485 | |||||||
| chr5:53587501 | T | A | 1 | a0001c0009t0001g0274 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.99-15951T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587501 | |||||||
| chr5:53587511 | C | T | 1 | a0001c0003t0002g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.99-15941C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587511 | |||||||
| chr5:53587580 | CT | C | 260 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(257): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.99-15857delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53587580 | ||||||
| chr5:53587580 | CTT | C | 18 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(15): Show |
18 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.99-15858_99-15857d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53587580 | ||||||
| chr5:53587824 | C | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.99-15628C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587824 | |||||||
| chr5:53587848 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | NA19067.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.99-15604G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587848 | |||||||
| chr5:53587857 | G | A | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.99-15595G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587857 | |||||||
| chr5:53587885 | C | G | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.99-15567C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587885 | |||||||
| chr5:53587895 | G | A | 7 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0049 others(4): Show |
7 | HG00741.hp1 HG01123.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.99-15557G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53587895 | |||||||
| chr5:53588044 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99-15408A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588044 | |||||||
| chr5:53588086 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.99-15366G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588086 | |||||||
| chr5:53588159 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99-15293C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588159 | |||||||
| chr5:53588292 | C | A | 5 | a0001c0002t0001g0157 a0001c0002t0001g0161 a0001c0002t0001g0163 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-15160C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588292 | |||||||
| chr5:53588305 | C | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.99-15147C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588305 | |||||||
| chr5:53588492 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.99-14960T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588492 | |||||||
| chr5:53588556 | A | G | 1 | a0001c0001t0004g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.99-14896A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588556 | |||||||
| chr5:53588609 | T | A | 1 | a0001c0001t0001g0293 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.99-14843T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588609 | |||||||
| chr5:53588734 | G | A | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.99-14718G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588734 | |||||||
| chr5:53588781 | A | G | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.99-14671A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588781 | |||||||
| chr5:53588784 | A | G | 106 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(103): Show |
107 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.99-14668A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588784 | |||||||
| chr5:53588799 | T | C | 8 | a0001c0001t0002g0175 a0001c0001t0002g0194 a0001c0001t0002g0195 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.99-14653T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588799 | |||||||
| chr5:53588803 | G | A | 105 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(102): Show |
106 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.99-14649G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588803 | |||||||
| chr5:53588816 | A | C | 1 | a0001c0001t0002g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.99-14636A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588816 | |||||||
| chr5:53588898 | A | T | 1 | a0001c0001t0002g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99-14554A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588898 | |||||||
| chr5:53588922 | A | T | 53 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(50): Show |
56 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.99-14530A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53588922 | |||||||
| chr5:53588984 | TA | T | 20 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(17): Show |
20 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.99-14457delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53588984 | ||||||
| chr5:53589107 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.99-14345A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53589107 | |||||||
| chr5:53589197 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99-14255A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53589197 | |||||||
| chr5:53589270 | A | G | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.99-14182A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53589270 | |||||||
| chr5:53589425 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.99-14027A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53589425 | |||||||
| chr5:53589469 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-13983A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53589469 | |||||||
| chr5:53589506 | C | G | 14 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(11): Show |
14 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.99-13946C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53589506 | |||||||
| chr5:53589649 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.99-13803A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53589649 | |||||||
| chr5:53589736 | C | G | 5 | a0001c0002t0001g0157 a0001c0002t0001g0161 a0001c0002t0001g0163 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-13716C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53589736 | |||||||
| chr5:53589926 | A | G | 1 | a0001c0001t0001g0360 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.99-13526A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53589926 | |||||||
| chr5:53590012 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-13440C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590012 | |||||||
| chr5:53590053 | C | G | 44 | a0001c0003t0002g0001 a0001c0003t0002g0099 a0001c0003t0002g0100 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.99-13399C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590053 | |||||||
| chr5:53590113 | A | G | 5 | a0001c0002t0001g0157 a0001c0002t0001g0161 a0001c0002t0001g0163 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-13339A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590113 | |||||||
| chr5:53590124 | A | T | 148 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(145): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.99-13328A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590124 | |||||||
| chr5:53590125 | A | T | 1 | a0001c0001t0002g0221 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.99-13327A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590125 | |||||||
| chr5:53590310 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.99-13142T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590310 | |||||||
| chr5:53590323 | C | T | 3 | a0001c0002t0001g0157 a0001c0002t0001g0161 a0001c0002t0001g0163 |
3 | HG02451.hp1 HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.99-13129C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590323 | |||||||
| chr5:53590437 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.99-13015T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590437 | |||||||
| chr5:53590467 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.99-12985A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590467 | |||||||
| chr5:53590669 | T | C | 1 | a0001c0003t0002g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99-12783T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590669 | |||||||
| chr5:53590726 | G | A | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.99-12726G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590726 | |||||||
| chr5:53590940 | T | C | 15 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(12): Show |
15 | HG01243.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.99-12512T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53590940 | |||||||
| chr5:53591036 | C | A | 37 | a0001c0002t0001g0040 a0001c0002t0001g0047 a0001c0002t0001g0048 others(34): Show |
37 | HG00323.hp1 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.99-12416C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591036 | |||||||
| chr5:53591060 | T | A | 2 | a0001c0001t0002g0152 a0001c0001t0002g0154 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.99-12392T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591060 | |||||||
| chr5:53591252 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.99-12200T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591252 | |||||||
| chr5:53591333 | A | C | 1 | a0001c0002t0001g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.99-12119A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591333 | |||||||
| chr5:53591419 | T | G | 1 | a0001c0004t0001g0038 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.99-12033T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591419 | |||||||
| chr5:53591461 | T | G | 2 | a0001c0001t0002g0238 a0001c0004t0001g0038 |
2 | HG01261.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.99-11991T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591461 | |||||||
| chr5:53591461 | T | TG | 63 | a0001c0001t0001g0006 a0001c0001t0001g0251 a0001c0001t0001g0252 others(60): Show |
64 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.99-11979dupG | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53591461 | ||||||
| chr5:53591461 | T | TGG | 34 | a0001c0001t0001g0263 a0001c0001t0001g0276 a0001c0001t0001g0280 others(31): Show |
34 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.99-11980_99-11979d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53591461 | ||||||
| chr5:53591461 | TG | T | 139 | a0001c0001t0001g0142 a0001c0001t0001g0171 a0001c0001t0001g0173 others(136): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.99-11979delG | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53591461 | ||||||
| chr5:53591462 | G | T | 1 | a0001c0001t0001g0295 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.99-11990G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591462 | |||||||
| chr5:53591463 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.99-11989G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591463 | |||||||
| chr5:53591464 | G | C | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.99-11988G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591464 | |||||||
| chr5:53591466 | G | T | 5 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0357 others(2): Show |
5 | NA18939.hp2 NA18952.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-11986G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591466 | |||||||
| chr5:53591483 | C | T | 44 | a0001c0003t0002g0001 a0001c0003t0002g0099 a0001c0003t0002g0100 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.99-11969C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591483 | |||||||
| chr5:53591616 | A | G | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.99-11836A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591616 | |||||||
| chr5:53591776 | T | G | 1 | a0001c0001t0001g0326 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.99-11676T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591776 | |||||||
| chr5:53591890 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.99-11562T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53591890 | |||||||
| chr5:53591935 | TTTGTTG | T | 6 | a0001c0003t0002g0125 a0001c0003t0002g0126 a0001c0003t0002g0127 others(3): Show |
6 | HG02155.hp2 NA18962.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-11505_99-11500d others(8): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53591935 | ||||||
| chr5:53592085 | C | T | 1 | a0001c0001t0001g0360 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.99-11367C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53592085 | |||||||
| chr5:53592146 | T | G | 1 | a0002c0005t0002g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99-11306T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53592146 | |||||||
| chr5:53592199 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.99-11253G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53592199 | |||||||
| chr5:53592212 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.99-11240A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53592212 | |||||||
| chr5:53592243 | C | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0009t0001g0274 |
3 | HG01884.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99-11209C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53592243 | |||||||
| chr5:53592378 | A | G | 1 | a0001c0003t0002g0130 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.99-11074A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53592378 | |||||||
| chr5:53592432 | T | C | 3 | a0001c0001t0002g0226 a0001c0003t0002g0227 a0001c0003t0002g0228 |
3 | NA18974.hp1 NA18995.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.99-11020T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53592432 | |||||||
| chr5:53592759 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.99-10693T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53592759 | |||||||
| chr5:53592864 | T | C | 8 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0043 others(5): Show |
8 | HG01175.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.99-10588T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53592864 | |||||||
| chr5:53592886 | G | A | 250 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0271 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.99-10566G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53592886 | |||||||
| chr5:53593043 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-10409G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53593043 | |||||||
| chr5:53593112 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99-10340G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53593112 | |||||||
| chr5:53593571 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99-9881T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53593571 | |||||||
| chr5:53593600 | C | CT | 30 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(27): Show |
30 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.99-9841dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53593600 | ||||||
| chr5:53593600 | CT | C | 53 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(50): Show |
56 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.99-9841delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53593600 | ||||||
| chr5:53593670 | T | A | 1 | a0001c0001t0001g0273 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.99-9782T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53593670 | |||||||
| chr5:53593671 | A | T | 1 | a0001c0001t0001g0273 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.99-9781A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53593671 | |||||||
| chr5:53593779 | A | G | 3 | a0001c0001t0002g0199 a0001c0001t0002g0203 a0001c0001t0002g0204 |
3 | HG00323.hp2 HG00738.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.99-9673A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53593779 | |||||||
| chr5:53593813 | T | C | 1 | a0001c0001t0001g0357 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.99-9639T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53593813 | |||||||
| chr5:53593830 | G | C | 1 | a0001c0001t0001g0360 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.99-9622G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53593830 | |||||||
| chr5:53593837 | A | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(88): Show |
92 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.99-9615A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53593837 | |||||||
| chr5:53593969 | C | T | 1 | a0001c0003t0002g0228 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.99-9483C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53593969 | |||||||
| chr5:53594123 | A | G | 53 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(50): Show |
56 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.99-9329A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53594123 | |||||||
| chr5:53594275 | A | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.99-9177A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53594275 | |||||||
| chr5:53594324 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.99-9128C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53594324 | |||||||
| chr5:53594325 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.99-9127G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53594325 | |||||||
| chr5:53594430 | A | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.99-9022A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53594430 | |||||||
| chr5:53594564 | CTCATA | C | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.99-8883_99-8879del others(5): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53594564 | ||||||
| chr5:53594866 | C | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99-8586C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53594866 | |||||||
| chr5:53594872 | T | TTG | 114 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(111): Show |
115 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.99-8554_99-8553dup others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53594872 | ||||||
| chr5:53594872 | T | TTGTG | 35 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(32): Show |
35 | HG00140.hp1 HG00438.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.99-8556_99-8553dup others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53594872 | ||||||
| chr5:53594872 | T | TTGTGTG | 3 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0001g0344 |
3 | HG03486.hp2 NA18906.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.99-8558_99-8553dup others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53594872 | ||||||
| chr5:53594872 | T | TTGTGTGT others(1): Show |
9 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0170 others(6): Show |
9 | HG01884.hp2 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-8560_99-8553dup others(8): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53594872 | ||||||
| chr5:53594872 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0166 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.99-8562_99-8553dup others(10): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53594872 | ||||||
| chr5:53594872 | TTG | T | 62 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(59): Show |
65 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.99-8554_99-8553del others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53594872 | ||||||
| chr5:53594896 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.99-8556G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53594896 | |||||||
| chr5:53594900 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG01167.hp1 HG01255.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.99-8552A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53594900 | |||||||
| chr5:53594972 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-8480C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53594972 | |||||||
| chr5:53594981 | T | A | 1 | a0001c0003t0002g0116 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.99-8471T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53594981 | |||||||
| chr5:53595031 | C | G | 53 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(50): Show |
56 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.99-8421C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595031 | |||||||
| chr5:53595201 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.99-8251T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595201 | |||||||
| chr5:53595280 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.99-8172A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595280 | |||||||
| chr5:53595303 | A | G | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0009t0001g0274 |
3 | HG01884.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99-8149A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595303 | |||||||
| chr5:53595601 | C | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.99-7851C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595601 | |||||||
| chr5:53595621 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.99-7831G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595621 | |||||||
| chr5:53595699 | T | A | 1 | a0001c0001t0002g0096 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.99-7753T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595699 | |||||||
| chr5:53595709 | G | T | 3 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0153 |
3 | HG02257.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.99-7743G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595709 | |||||||
| chr5:53595822 | A | G | 2 | a0001c0002t0001g0007 a0001c0002t0001g0008 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.99-7630A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595822 | |||||||
| chr5:53595832 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.99-7620G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595832 | |||||||
| chr5:53595937 | G | A | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.99-7515G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595937 | |||||||
| chr5:53595990 | A | G | 1 | a0001c0001t0001g0340 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.99-7462A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53595990 | |||||||
| chr5:53596018 | A | G | 133 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(130): Show |
134 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.99-7434A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596018 | |||||||
| chr5:53596119 | G | A | 2 | a0001c0004t0001g0026 a0001c0004t0001g0039 |
2 | NA18983.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.99-7333G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596119 | |||||||
| chr5:53596147 | T | C | 3 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0162 |
3 | HG02486.hp1 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.99-7305T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596147 | |||||||
| chr5:53596242 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.99-7210G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596242 | |||||||
| chr5:53596267 | T | TA | 101 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(98): Show |
102 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.99-7176dupA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53596267 | ||||||
| chr5:53596366 | G | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99-7086G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596366 | |||||||
| chr5:53596406 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.99-7046G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596406 | |||||||
| chr5:53596476 | T | C | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.99-6976T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596476 | |||||||
| chr5:53596527 | G | A | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.99-6925G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596527 | |||||||
| chr5:53596613 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99-6839A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596613 | |||||||
| chr5:53596684 | T | G | 1 | a0001c0001t0001g0313 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.99-6768T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596684 | |||||||
| chr5:53596790 | G | A | 169 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(166): Show |
173 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.99-6662G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596790 | |||||||
| chr5:53596843 | G | T | 1 | a0001c0001t0001g0303 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99-6609G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596843 | |||||||
| chr5:53596964 | A | G | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.99-6488A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53596964 | |||||||
| chr5:53597015 | T | C | 1 | a0001c0003t0002g0117 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.99-6437T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597015 | |||||||
| chr5:53597021 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.99-6431G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597021 | |||||||
| chr5:53597123 | A | T | 105 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(102): Show |
106 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.99-6329A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597123 | |||||||
| chr5:53597382 | A | G | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.99-6070A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597382 | |||||||
| chr5:53597409 | A | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(88): Show |
92 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.99-6043A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597409 | |||||||
| chr5:53597514 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99-5938A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597514 | |||||||
| chr5:53597603 | AAAAGTGT others(6): Show |
A | 1 | a0001c0001t0004g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.99-5846_99-5834del others(13): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53597603 | ||||||
| chr5:53597666 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99-5786C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597666 | |||||||
| chr5:53597783 | C | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99-5669C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597783 | |||||||
| chr5:53597851 | G | A | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.99-5601G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597851 | |||||||
| chr5:53597856 | T | G | 1 | a0001c0002t0001g0007 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.99-5596T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597856 | |||||||
| chr5:53597876 | A | G | 1 | a0001c0003t0002g0129 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.99-5576A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597876 | |||||||
| chr5:53597883 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-5569A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597883 | |||||||
| chr5:53597961 | A | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0009t0001g0274 |
3 | HG01884.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99-5491A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597961 | |||||||
| chr5:53597979 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99-5473A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53597979 | |||||||
| chr5:53598044 | A | G | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.99-5408A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598044 | |||||||
| chr5:53598048 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99-5404A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598048 | |||||||
| chr5:53598072 | A | G | 1 | a0001c0003t0002g0116 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.99-5380A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598072 | |||||||
| chr5:53598181 | A | AAG | 262 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.99-5268_99-5267dup others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53598181 | ||||||
| chr5:53598224 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.99-5228G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598224 | |||||||
| chr5:53598429 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-5023C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598429 | |||||||
| chr5:53598446 | T | A | 262 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.99-5006T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598446 | |||||||
| chr5:53598475 | G | C | 1 | a0001c0001t0002g0229 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.99-4977G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598475 | |||||||
| chr5:53598495 | A | G | 1 | a0001c0001t0001g0347 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.99-4957A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598495 | |||||||
| chr5:53598520 | T | C | 1 | a0001c0003t0002g0120 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.99-4932T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598520 | |||||||
| chr5:53598645 | C | T | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0359 |
3 | HG00438.hp1 HG02056.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.99-4807C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598645 | |||||||
| chr5:53598768 | A | G | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.99-4684A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53598768 | |||||||
| chr5:53599006 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.99-4446C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53599006 | |||||||
| chr5:53599018 | A | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.99-4434A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53599018 | |||||||
| chr5:53599041 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.99-4411A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53599041 | |||||||
| chr5:53599208 | T | C | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99-4244T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53599208 | |||||||
| chr5:53599344 | A | T | 2 | a0001c0002t0001g0048 a0001c0002t0001g0050 |
2 | HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.99-4108A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53599344 | |||||||
| chr5:53599403 | G | A | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.99-4049G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53599403 | |||||||
| chr5:53599437 | C | T | 8 | a0001c0001t0002g0177 a0001c0001t0002g0189 a0001c0001t0002g0199 others(5): Show |
8 | HG00323.hp2 HG00738.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.99-4015C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53599437 | |||||||
| chr5:53599556 | A | G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.99-3896A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53599556 | |||||||
| chr5:53599590 | A | C | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0009t0001g0274 |
3 | HG01884.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99-3862A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53599590 | |||||||
| chr5:53600154 | C | T | 6 | a0001c0001t0002g0199 a0001c0001t0002g0203 a0001c0001t0002g0204 others(3): Show |
6 | HG00323.hp2 HG00738.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-3298C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600154 | |||||||
| chr5:53600234 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.99-3218G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600234 | |||||||
| chr5:53600295 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.99-3157G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600295 | |||||||
| chr5:53600297 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.99-3155C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600297 | |||||||
| chr5:53600367 | T | C | 1 | a0001c0001t0001g0317 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.99-3085T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600367 | |||||||
| chr5:53600417 | T | C | 1 | a0001c0003t0002g0120 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.99-3035T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600417 | |||||||
| chr5:53600429 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99-3023C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600429 | |||||||
| chr5:53600490 | G | A | 82 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
86 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.99-2962G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600490 | |||||||
| chr5:53600568 | T | C | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.99-2884T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600568 | |||||||
| chr5:53600601 | G | A | 1 | a0001c0001t0001g0356 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.99-2851G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600601 | |||||||
| chr5:53600603 | C | A | 13 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG01109.hp1 HG01433.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.99-2849C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600603 | |||||||
| chr5:53600822 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.99-2630T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600822 | |||||||
| chr5:53600861 | C | G | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.99-2591C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600861 | |||||||
| chr5:53600893 | C | T | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.99-2559C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600893 | |||||||
| chr5:53600914 | G | T | 1 | a0001c0003t0002g0104 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.99-2538G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600914 | |||||||
| chr5:53600970 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG01167.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.99-2482A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600970 | |||||||
| chr5:53600987 | C | T | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.99-2465C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53600987 | |||||||
| chr5:53601003 | A | AT | 22 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0170 others(19): Show |
22 | HG00438.hp1 HG02027.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.99-2430dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53601003 | ||||||
| chr5:53601003 | AT | A | 90 | a0001c0001t0001g0142 a0001c0001t0001g0272 a0001c0001t0001g0277 others(87): Show |
94 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.99-2430delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53601003 | ||||||
| chr5:53601003 | ATT | A | 59 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0102 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.99-2431_99-2430del others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53601003 | ||||||
| chr5:53601057 | T | G | 3 | a0001c0001t0001g0318 a0001c0001t0001g0327 a0001c0001t0001g0345 |
3 | HG02004.hp1 HG02300.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.99-2395T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53601057 | |||||||
| chr5:53601085 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99-2367A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53601085 | |||||||
| chr5:53601090 | C | T | 15 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(12): Show |
15 | HG01243.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.99-2362C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53601090 | |||||||
| chr5:53601153 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.99-2299G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53601153 | |||||||
| chr5:53601165 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.99-2287G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53601165 | |||||||
| chr5:53601205 | G | A | 3 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0207 |
3 | HG01257.hp1 HG01258.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.99-2247G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53601205 | |||||||
| chr5:53601477 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.99-1975A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53601477 | |||||||
| chr5:53601734 | T | C | 1 | a0001c0002t0001g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.99-1718T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53601734 | |||||||
| chr5:53601777 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-1675G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53601777 | |||||||
| chr5:53601851 | C | A | 1 | a0001c0004t0001g0084 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.99-1601C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53601851 | |||||||
| chr5:53602001 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.99-1451C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602001 | |||||||
| chr5:53602034 | C | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.99-1418C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602034 | |||||||
| chr5:53602050 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.99-1402G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602050 | |||||||
| chr5:53602068 | G | A | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.99-1384G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602068 | |||||||
| chr5:53602180 | T | C | 1 | a0001c0001t0001g0360 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.99-1272T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602180 | |||||||
| chr5:53602259 | A | G | 2 | a0001c0002t0001g0157 a0001c0002t0001g0161 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.99-1193A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602259 | |||||||
| chr5:53602333 | C | T | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99-1119C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602333 | |||||||
| chr5:53602352 | T | C | 9 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0299 others(6): Show |
9 | HG01346.hp1 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.99-1100T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602352 | |||||||
| chr5:53602733 | A | G | 1 | a0001c0003t0002g0228 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.99-719A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602733 | |||||||
| chr5:53602851 | A | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.99-601A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602851 | |||||||
| chr5:53602931 | T | G | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.99-521T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53602931 | |||||||
| chr5:53603068 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.99-384T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53603068 | |||||||
| chr5:53603084 | T | G | 1 | a0001c0003t0002g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99-368T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53603084 | |||||||
| chr5:53603226 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-226G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | chr5 | 53603226 | |||||||
| chr5:53603336 | C | CT | 115 | a0001c0001t0001g0272 a0001c0001t0001g0328 a0001c0001t0002g0003 others(112): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.99-101dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53603336 | ||||||
| chr5:53603336 | C | CTT | 28 | a0001c0001t0001g0142 a0001c0001t0001g0164 a0001c0001t0001g0165 others(25): Show |
28 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.99-102_99-101dupTT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53603336 | ||||||
| chr5:53603336 | C | CTTT | 106 | a0001c0001t0001g0006 a0001c0001t0001g0251 a0001c0001t0001g0252 others(103): Show |
107 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.99-103_99-101dupTT others(1): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 53603336 | ||||||
| chr5:53603703 | G | A | 2 | a0001c0001t0001g0337 a0001c0001t0001g0372 |
2 | HG02027.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.177+173G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53603703 | |||||||
| chr5:53603756 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0350 a0001c0001t0001g0351 |
4 | NA18966.hp1 NA18980.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+226A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53603756 | |||||||
| chr5:53603944 | A | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.177+414A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53603944 | |||||||
| chr5:53604109 | A | T | 133 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(130): Show |
134 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.177+579A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53604109 | |||||||
| chr5:53604426 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG01167.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.177+896C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53604426 | |||||||
| chr5:53604688 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.177+1158C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53604688 | |||||||
| chr5:53604812 | T | G | 1 | a0001c0001t0001g0328 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.177+1282T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53604812 | |||||||
| chr5:53604970 | C | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+1440C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53604970 | |||||||
| chr5:53605175 | C | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+1645C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605175 | |||||||
| chr5:53605335 | C | T | 6 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG02723.hp2 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+1805C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605335 | |||||||
| chr5:53605356 | T | G | 4 | a0001c0002t0001g0066 a0001c0002t0001g0068 a0001c0002t0001g0069 others(1): Show |
4 | NA18970.hp2 NA18994.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+1826T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605356 | |||||||
| chr5:53605448 | A | T | 82 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
86 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.177+1918A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605448 | |||||||
| chr5:53605526 | T | C | 1 | a0003c0006t0002g0093 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.177+1996T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605526 | |||||||
| chr5:53605570 | C | G | 112 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0095 others(109): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.177+2040C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605570 | |||||||
| chr5:53605577 | G | A | 1 | a0001c0004t0001g0026 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.177+2047G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605577 | |||||||
| chr5:53605663 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.177+2133A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605663 | |||||||
| chr5:53605675 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.177+2145C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605675 | |||||||
| chr5:53605709 | A | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+2179A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605709 | |||||||
| chr5:53605879 | C | T | 6 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(3): Show |
6 | HG01496.hp1 HG01928.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+2349C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605879 | |||||||
| chr5:53605979 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.177+2449A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605979 | |||||||
| chr5:53605992 | C | T | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.177+2462C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53605992 | |||||||
| chr5:53606008 | C | T | 4 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0367 others(1): Show |
4 | HG00639.hp2 HG01123.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+2478C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606008 | |||||||
| chr5:53606013 | C | CA | 34 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(31): Show |
34 | HG00741.hp1 HG01106.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.177+2504dupA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53606013 | ||||||
| chr5:53606013 | CA | C | 141 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0275 others(138): Show |
145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.177+2504delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53606013 | ||||||
| chr5:53606013 | CAA | C | 13 | a0001c0001t0001g0276 a0001c0001t0001g0336 a0001c0001t0002g0179 others(10): Show |
13 | HG00099.hp1 HG00733.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.177+2503_177+2504d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53606013 | ||||||
| chr5:53606048 | G | A | 105 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(102): Show |
106 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.177+2518G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606048 | |||||||
| chr5:53606082 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.177+2552G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606082 | |||||||
| chr5:53606115 | C | A | 92 | a0001c0001t0002g0002 a0001c0001t0002g0095 a0001c0001t0002g0102 others(89): Show |
94 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.177+2585C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606115 | |||||||
| chr5:53606255 | C | T | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | NA19010.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.177+2725C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606255 | |||||||
| chr5:53606358 | A | G | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.177+2828A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606358 | |||||||
| chr5:53606408 | T | C | 280 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.177+2878T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606408 | |||||||
| chr5:53606414 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+2884C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606414 | |||||||
| chr5:53606430 | C | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.177+2900C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606430 | |||||||
| chr5:53606477 | A | G | 187 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(184): Show |
191 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.177+2947A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606477 | |||||||
| chr5:53606555 | C | T | 4 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
4 | HG01109.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+3025C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606555 | |||||||
| chr5:53606605 | T | C | 1 | a0001c0003t0002g0109 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.177+3075T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606605 | |||||||
| chr5:53606624 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.177+3094C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606624 | |||||||
| chr5:53606665 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.177+3135C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606665 | |||||||
| chr5:53606770 | G | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(95): Show |
99 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.177+3240G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606770 | |||||||
| chr5:53606797 | A | G | 1 | a0001c0004t0001g0087 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.177+3267A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606797 | |||||||
| chr5:53606877 | A | G | 1 | a0001c0001t0001g0368 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.177+3347A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606877 | |||||||
| chr5:53606960 | G | T | 1 | a0001c0001t0001g0362 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.177+3430G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53606960 | |||||||
| chr5:53607024 | C | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.177+3494C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607024 | |||||||
| chr5:53607064 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.177+3534C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607064 | |||||||
| chr5:53607065 | A | G | 287 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(284): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.177+3535A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607065 | |||||||
| chr5:53607075 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.177+3545G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607075 | |||||||
| chr5:53607148 | A | G | 8 | a0001c0001t0002g0249 a0001c0001t0002g0250 a0001c0002t0001g0157 others(5): Show |
8 | HG02451.hp1 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+3618A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607148 | |||||||
| chr5:53607229 | C | T | 3 | a0001c0001t0002g0243 a0001c0004t0001g0023 a0001c0004t0001g0024 |
3 | NA18939.hp1 NA18964.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.177+3699C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607229 | |||||||
| chr5:53607234 | T | C | 55 | a0001c0001t0001g0276 a0001c0001t0001g0322 a0001c0001t0001g0337 others(52): Show |
55 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.177+3704T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607234 | |||||||
| chr5:53607274 | A | C | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0202 |
3 | HG00741.hp2 HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.177+3744A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607274 | |||||||
| chr5:53607528 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.177+3998C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607528 | |||||||
| chr5:53607530 | G | A | 1 | a0001c0004t0001g0015 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.177+4000G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607530 | |||||||
| chr5:53607636 | G | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.177+4106G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607636 | |||||||
| chr5:53607704 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG01167.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.177+4174A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607704 | |||||||
| chr5:53607785 | A | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+4255A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607785 | |||||||
| chr5:53607957 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0261 |
2 | NA18951.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.177+4427A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607957 | |||||||
| chr5:53607972 | TACATTA | T | 4 | a0001c0001t0001g0316 a0001c0001t0001g0329 a0001c0001t0001g0336 others(1): Show |
4 | HG00673.hp1 NA18986.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+4444_177+4449d others(8): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53607972 | ||||||
| chr5:53607974 | C | A | 131 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(128): Show |
132 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.177+4444C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607974 | |||||||
| chr5:53607981 | T | A | 4 | a0001c0001t0001g0316 a0001c0001t0001g0329 a0001c0001t0001g0336 others(1): Show |
4 | HG00673.hp1 NA18986.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+4451T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53607981 | |||||||
| chr5:53608092 | G | A | 133 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(130): Show |
134 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.177+4562G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608092 | |||||||
| chr5:53608120 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.177+4590G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608120 | |||||||
| chr5:53608130 | C | A | 1 | a0001c0002t0001g0057 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.177+4600C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608130 | |||||||
| chr5:53608172 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.177+4642G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608172 | |||||||
| chr5:53608231 | C | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.177+4701C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608231 | |||||||
| chr5:53608317 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.177+4787G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608317 | |||||||
| chr5:53608404 | T | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.177+4874T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608404 | |||||||
| chr5:53608565 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.177+5035A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608565 | |||||||
| chr5:53608599 | C | T | 1 | a0001c0001t0001g0361 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.177+5069C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608599 | |||||||
| chr5:53608610 | A | C | 3 | a0001c0003t0002g0130 a0001c0003t0002g0139 a0001c0003t0002g0140 |
3 | HG01071.hp1 HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.177+5080A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608610 | |||||||
| chr5:53608616 | GA | G | 132 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(129): Show |
133 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.177+5087delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608616 | |||||||
| chr5:53608830 | T | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.177+5300T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608830 | |||||||
| chr5:53608833 | A | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.177+5303A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608833 | |||||||
| chr5:53608834 | A | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.177+5304A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53608834 | |||||||
| chr5:53609134 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.177+5604T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609134 | |||||||
| chr5:53609164 | C | G | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.177+5634C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609164 | |||||||
| chr5:53609246 | ATAAT | A | 6 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(3): Show |
6 | HG01496.hp1 HG01928.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+5717_177+5720d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609246 | |||||||
| chr5:53609256 | T | G | 1 | a0001c0001t0002g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.177+5726T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609256 | |||||||
| chr5:53609409 | A | T | 1 | a0001c0009t0001g0274 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.177+5879A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609409 | |||||||
| chr5:53609479 | T | G | 1 | a0001c0002t0001g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.177+5949T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609479 | |||||||
| chr5:53609560 | A | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0289 a0001c0001t0001g0290 others(48): Show |
52 | HG00423.hp2 HG00609.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.177+6030A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609560 | |||||||
| chr5:53609635 | A | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.177+6105A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609635 | |||||||
| chr5:53609647 | C | G | 1 | a0001c0003t0002g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.177+6117C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609647 | |||||||
| chr5:53609765 | C | G | 1 | a0001c0003t0002g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.177+6235C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609765 | |||||||
| chr5:53609774 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.177+6244G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609774 | |||||||
| chr5:53609813 | C | CT | 278 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.177+6284dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53609813 | ||||||
| chr5:53609813 | C | T | 2 | a0001c0002t0001g0063 a0001c0002t0001g0064 |
2 | HG00323.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.177+6283C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609813 | |||||||
| chr5:53609845 | C | A | 1 | a0001c0003t0002g0105 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.177+6315C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609845 | |||||||
| chr5:53609954 | C | T | 1 | a0001c0003t0002g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.177+6424C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609954 | |||||||
| chr5:53609963 | G | A | 1 | a0001c0001t0001g0352 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.177+6433G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609963 | |||||||
| chr5:53609963 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+6433G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53609963 | |||||||
| chr5:53610345 | A | C | 1 | a0001c0001t0001g0367 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.177+6815A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53610345 | |||||||
| chr5:53610391 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0001g0172 |
3 | HG03486.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.177+6861C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53610391 | |||||||
| chr5:53610417 | C | T | 250 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0271 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.177+6887C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53610417 | |||||||
| chr5:53610452 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.177+6922A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53610452 | |||||||
| chr5:53610541 | TA | T | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.177+7018delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53610541 | ||||||
| chr5:53610614 | C | T | 104 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(101): Show |
105 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.177+7084C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53610614 | |||||||
| chr5:53610853 | A | T | 1 | a0001c0002t0001g0057 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.177+7323A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53610853 | |||||||
| chr5:53610928 | G | A | 28 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(25): Show |
28 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.177+7398G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53610928 | |||||||
| chr5:53610938 | T | C | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.177+7408T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53610938 | |||||||
| chr5:53610994 | A | G | 3 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 |
3 | HG01081.hp1 HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.177+7464A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53610994 | |||||||
| chr5:53610997 | C | T | 1 | a0001c0001t0002g0210 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.177+7467C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53610997 | |||||||
| chr5:53611052 | GAGTCACT others(3): Show |
G | 1 | a0001c0001t0002g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.177+7525_177+7534d others(12): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53611052 | ||||||
| chr5:53611123 | A | G | 2 | a0001c0004t0001g0011 a0001c0004t0001g0018 |
2 | HG02293.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.177+7593A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53611123 | |||||||
| chr5:53611130 | A | G | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.177+7600A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53611130 | |||||||
| chr5:53611133 | C | T | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+7603C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53611133 | |||||||
| chr5:53611136 | T | C | 1 | a0001c0004t0001g0088 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.177+7606T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53611136 | |||||||
| chr5:53611191 | A | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0198 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.177+7661A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53611191 | |||||||
| chr5:53611205 | G | GT | 15 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(12): Show |
15 | HG01433.hp2 HG02055.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.177+7688dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53611205 | ||||||
| chr5:53611223 | G | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+7693G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53611223 | |||||||
| chr5:53611391 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.177+7861C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53611391 | |||||||
| chr5:53611418 | A | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0348 |
2 | HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.177+7888A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53611418 | |||||||
| chr5:53611585 | TA | T | 11 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(8): Show |
11 | HG00423.hp1 HG00558.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.177+8066delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53611585 | ||||||
| chr5:53611760 | G | A | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+8230G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53611760 | |||||||
| chr5:53611868 | A | G | 1 | a0001c0001t0001g0357 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.177+8338A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53611868 | |||||||
| chr5:53612012 | A | C | 1 | a0001c0001t0002g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.177+8482A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53612012 | |||||||
| chr5:53612170 | T | G | 3 | a0001c0001t0001g0142 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG01167.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.177+8640T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53612170 | |||||||
| chr5:53612375 | A | G | 278 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.177+8845A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53612375 | |||||||
| chr5:53612647 | G | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.177+9117G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53612647 | |||||||
| chr5:53612836 | A | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.177+9306A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53612836 | |||||||
| chr5:53613258 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.177+9728C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53613258 | |||||||
| chr5:53613379 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.177+9849A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53613379 | |||||||
| chr5:53613602 | G | GT | 65 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(62): Show |
66 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.177+10085dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53613602 | ||||||
| chr5:53613602 | GT | G | 14 | a0001c0001t0001g0142 a0001c0001t0001g0164 a0001c0001t0001g0165 others(11): Show |
14 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.177+10085delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53613602 | ||||||
| chr5:53613619 | A | G | 1 | a0001c0007t0002g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.177+10089A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53613619 | |||||||
| chr5:53613662 | G | GA | 9 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(6): Show |
9 | HG01934.hp2 HG02723.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+10145dupA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53613662 | ||||||
| chr5:53613662 | GA | G | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 others(5): Show |
8 | HG01109.hp1 HG01433.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+10145delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53613662 | ||||||
| chr5:53613776 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.177+10246G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53613776 | |||||||
| chr5:53613945 | T | C | 2 | a0001c0001t0001g0346 a0001c0001t0001g0347 |
2 | NA18952.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.177+10415T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53613945 | |||||||
| chr5:53613972 | A | C | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.177+10442A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53613972 | |||||||
| chr5:53614097 | C | T | 250 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0271 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.177+10567C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53614097 | |||||||
| chr5:53614106 | A | G | 250 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0271 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.177+10576A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53614106 | |||||||
| chr5:53614128 | T | A | 1 | a0001c0001t0001g0327 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.177+10598T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53614128 | |||||||
| chr5:53614166 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.177+10636A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53614166 | |||||||
| chr5:53614185 | G | T | 1 | a0001c0004t0001g0038 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.177+10655G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53614185 | |||||||
| chr5:53614217 | T | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+10687T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53614217 | |||||||
| chr5:53614662 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.177+11132C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53614662 | |||||||
| chr5:53614768 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.177+11238T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53614768 | |||||||
| chr5:53614909 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.177+11379G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53614909 | |||||||
| chr5:53615189 | T | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+11659T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53615189 | |||||||
| chr5:53615204 | C | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+11674C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53615204 | |||||||
| chr5:53615322 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.177+11792T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53615322 | |||||||
| chr5:53615327 | G | C | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.177+11797G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53615327 | |||||||
| chr5:53615406 | C | T | 2 | a0001c0003t0002g0112 a0001c0003t0002g0113 |
2 | NA19007.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.177+11876C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53615406 | |||||||
| chr5:53615496 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.177+11966T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53615496 | |||||||
| chr5:53615696 | A | G | 1 | a0002c0005t0002g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.177+12166A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53615696 | |||||||
| chr5:53615887 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.177+12357G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53615887 | |||||||
| chr5:53616036 | T | C | 2 | a0001c0001t0002g0192 a0001c0001t0002g0193 |
2 | HG00642.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.177+12506T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53616036 | |||||||
| chr5:53616217 | A | AT | 86 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(83): Show |
90 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.177+12699dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53616217 | ||||||
| chr5:53616240 | A | G | 1 | a0001c0002t0001g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.177+12710A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53616240 | |||||||
| chr5:53616268 | G | A | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.177+12738G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53616268 | |||||||
| chr5:53616414 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.177+12884G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53616414 | |||||||
| chr5:53616419 | G | A | 282 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(279): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.177+12889G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53616419 | |||||||
| chr5:53616524 | C | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0169 a0001c0001t0001g0171 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.177+12994C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53616524 | |||||||
| chr5:53616665 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.177+13135G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53616665 | |||||||
| chr5:53616699 | G | A | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.177+13169G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53616699 | |||||||
| chr5:53616701 | A | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.177+13171A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53616701 | |||||||
| chr5:53616921 | A | C | 45 | a0001c0002t0001g0046 a0001c0003t0002g0001 a0001c0003t0002g0099 others(42): Show |
46 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.177+13391A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53616921 | |||||||
| chr5:53617061 | A | C | 146 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(143): Show |
148 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.177+13531A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53617061 | |||||||
| chr5:53617137 | C | A | 1 | a0001c0001t0001g0362 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.177+13607C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53617137 | |||||||
| chr5:53617151 | T | C | 1 | a0001c0001t0002g0215 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.177+13621T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53617151 | |||||||
| chr5:53617243 | C | T | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.177+13713C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53617243 | |||||||
| chr5:53617473 | A | C | 1 | a0001c0001t0001g0297 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.177+13943A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53617473 | |||||||
| chr5:53617571 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.177+14041C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53617571 | |||||||
| chr5:53617689 | T | A | 2 | a0001c0001t0001g0341 a0001c0002t0001g0092 |
2 | HG03669.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.177+14159T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53617689 | |||||||
| chr5:53617862 | T | A | 1 | a0001c0001t0001g0311 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.177+14332T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53617862 | |||||||
| chr5:53618054 | A | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0254 a0001c0001t0001g0255 |
3 | HG00140.hp1 HG01169.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.177+14524A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618054 | |||||||
| chr5:53618105 | G | A | 135 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(132): Show |
136 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.177+14575G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618105 | |||||||
| chr5:53618129 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.177+14599G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618129 | |||||||
| chr5:53618276 | AAAAT | A | 82 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
86 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.177+14761_177+1476 others(8): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53618276 | ||||||
| chr5:53618381 | GAATTAT | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+14858_177+1486 others(10): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53618381 | ||||||
| chr5:53618386 | A | G | 1 | a0001c0009t0001g0274 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.177+14856A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618386 | |||||||
| chr5:53618642 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.177+15112C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618642 | |||||||
| chr5:53618741 | C | G | 3 | a0001c0003t0002g0136 a0001c0003t0002g0137 a0001c0003t0002g0138 |
3 | HG00673.hp2 HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.177+15211C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618741 | |||||||
| chr5:53618823 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+15293C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618823 | |||||||
| chr5:53618876 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.177+15346G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618876 | |||||||
| chr5:53618886 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.177+15356G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618886 | |||||||
| chr5:53618907 | A | G | 2 | a0001c0002t0001g0007 a0001c0002t0001g0008 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.177+15377A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618907 | |||||||
| chr5:53618943 | G | A | 4 | a0001c0001t0001g0333 a0001c0001t0001g0338 a0001c0001t0001g0339 others(1): Show |
4 | NA18981.hp2 NA19077.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+15413G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53618943 | |||||||
| chr5:53619114 | A | AAAT | 10 | a0001c0001t0002g0249 a0001c0001t0002g0250 a0001c0004t0001g0084 others(7): Show |
10 | HG00609.hp1 HG03130.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.177+15609_177+1561 others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53619114 | ||||||
| chr5:53619305 | TTA | T | 108 | a0001c0001t0001g0006 a0001c0001t0001g0165 a0001c0001t0001g0166 others(105): Show |
109 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.177+15776_177+1577 others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53619305 | |||||||
| chr5:53619305 | TTAA | T | 87 | a0001c0001t0001g0164 a0001c0001t0001g0272 a0001c0001t0001g0280 others(84): Show |
91 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.177+15776_177+1577 others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53619305 | |||||||
| chr5:53619306 | TA | T | 25 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0257 others(22): Show |
25 | HG00738.hp2 HG01099.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.177+15794delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53619306 | ||||||
| chr5:53619306 | TAAA | T | 61 | a0001c0001t0001g0142 a0001c0001t0002g0095 a0001c0001t0002g0102 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.177+15792_177+1579 others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53619306 | ||||||
| chr5:53619356 | G | C | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.177+15826G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53619356 | |||||||
| chr5:53619486 | C | CA | 40 | a0001c0001t0001g0142 a0001c0001t0001g0170 a0001c0001t0001g0173 others(37): Show |
41 | HG00438.hp2 HG00642.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.177+15978dupA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53619486 | ||||||
| chr5:53619486 | C | CAA | 85 | a0001c0001t0001g0006 a0001c0001t0001g0165 a0001c0001t0001g0166 others(82): Show |
86 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.177+15977_177+1597 others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53619486 | ||||||
| chr5:53619486 | C | CAAA | 37 | a0001c0001t0001g0164 a0001c0001t0001g0168 a0001c0001t0001g0257 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.177+15976_177+1597 others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53619486 | ||||||
| chr5:53619547 | A | G | 2 | a0001c0001t0001g0333 a0001c0001t0001g0339 |
2 | NA18981.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.177+16017A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53619547 | |||||||
| chr5:53619656 | C | A | 143 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(140): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.177+16126C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53619656 | |||||||
| chr5:53619686 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.177+16156T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53619686 | |||||||
| chr5:53619820 | G | A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+16290G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53619820 | |||||||
| chr5:53619887 | A | T | 1 | a0001c0001t0002g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.177+16357A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53619887 | |||||||
| chr5:53619915 | C | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+16385C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53619915 | |||||||
| chr5:53620188 | G | A | 278 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.177+16658G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53620188 | |||||||
| chr5:53620192 | T | G | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.177+16662T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53620192 | |||||||
| chr5:53620422 | A | G | 1 | a0001c0002t0001g0079 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+16892A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53620422 | |||||||
| chr5:53620515 | A | G | 7 | a0001c0001t0002g0216 a0001c0001t0002g0218 a0001c0001t0002g0219 others(4): Show |
7 | HG01928.hp2 HG01934.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+16985A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53620515 | |||||||
| chr5:53620662 | C | T | 22 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(19): Show |
22 | HG01109.hp1 HG01346.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.177+17132C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53620662 | |||||||
| chr5:53620796 | T | C | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.177+17266T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53620796 | |||||||
| chr5:53620854 | G | A | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.177+17324G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53620854 | |||||||
| chr5:53620866 | G | C | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+17336G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53620866 | |||||||
| chr5:53621130 | G | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+17600G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621130 | |||||||
| chr5:53621182 | C | T | 1 | a0001c0001t0002g0004 | 2 | NA19007.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.177+17652C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621182 | |||||||
| chr5:53621607 | A | G | 1 | a0001c0001t0002g0236 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.177+18077A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621607 | |||||||
| chr5:53621690 | A | AT | 37 | a0001c0001t0001g0142 a0001c0001t0001g0306 a0001c0001t0001g0307 others(34): Show |
37 | HG00438.hp2 HG00558.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.177+18189dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53621690 | ||||||
| chr5:53621690 | A | ATT | 9 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0002t0001g0040 others(6): Show |
9 | HG01952.hp1 HG02738.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.177+18188_177+1818 others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53621690 | ||||||
| chr5:53621690 | AT | A | 105 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(102): Show |
106 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.177+18189delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53621690 | ||||||
| chr5:53621690 | ATT | A | 86 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0313 others(83): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.177+18188_177+1818 others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53621690 | ||||||
| chr5:53621690 | ATTTTT | A | 10 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(7): Show |
10 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.177+18185_177+1818 others(9): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53621690 | ||||||
| chr5:53621690 | ATTTTTTT others(2): Show |
A | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+18181_177+1818 others(13): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53621690 | ||||||
| chr5:53621690 | ATTTTTTT others(7): Show |
A | 1 | a0001c0003t0002g0133 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.177+18176_177+1818 others(18): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53621690 | ||||||
| chr5:53621733 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.177+18203G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621733 | |||||||
| chr5:53621757 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.177+18227A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621757 | |||||||
| chr5:53621795 | G | T | 2 | a0001c0003t0002g0227 a0001c0003t0002g0228 |
2 | NA18974.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.177+18265G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621795 | |||||||
| chr5:53621836 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.177+18306G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621836 | |||||||
| chr5:53621903 | T | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+18373T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621903 | |||||||
| chr5:53621947 | G | A | 44 | a0001c0003t0002g0001 a0001c0003t0002g0099 a0001c0003t0002g0100 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.177+18417G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621947 | |||||||
| chr5:53621952 | G | T | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.177+18422G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621952 | |||||||
| chr5:53621980 | G | A | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.177+18450G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53621980 | |||||||
| chr5:53622003 | AATT | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0001g0172 |
3 | HG03486.hp2 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.177+18480_177+1848 others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53622003 | ||||||
| chr5:53622187 | A | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.177+18657A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53622187 | |||||||
| chr5:53622632 | A | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.177+19102A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53622632 | |||||||
| chr5:53622829 | C | T | 2 | a0001c0001t0001g0369 a0001c0001t0001g0370 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.177+19299C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53622829 | |||||||
| chr5:53622896 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.177+19366C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53622896 | |||||||
| chr5:53622908 | A | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+19378A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53622908 | |||||||
| chr5:53622972 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.177+19442A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53622972 | |||||||
| chr5:53623027 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.177+19497G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623027 | |||||||
| chr5:53623058 | G | A | 146 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.177+19528G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623058 | |||||||
| chr5:53623169 | C | T | 2 | a0001c0003t0002g0106 a0001c0003t0002g0107 |
2 | HG01069.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.177+19639C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623169 | |||||||
| chr5:53623208 | T | G | 1 | a0001c0003t0002g0149 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.177+19678T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623208 | |||||||
| chr5:53623349 | T | C | 1 | a0001c0001t0002g0236 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.177+19819T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623349 | |||||||
| chr5:53623392 | TGTTTATT others(4): Show |
T | 1 | a0001c0001t0002g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.177+19869_177+1987 others(15): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53623392 | ||||||
| chr5:53623434 | A | G | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.177+19904A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623434 | |||||||
| chr5:53623459 | G | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.177+19929G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623459 | |||||||
| chr5:53623518 | A | G | 2 | a0001c0002t0001g0007 a0001c0002t0001g0008 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.177+19988A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623518 | |||||||
| chr5:53623537 | A | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.177+20007A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623537 | |||||||
| chr5:53623715 | T | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.177+20185T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623715 | |||||||
| chr5:53623722 | CTTGT | C | 6 | a0001c0003t0002g0001 a0001c0003t0002g0103 a0001c0003t0002g0108 others(3): Show |
7 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+20203_177+2020 others(8): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53623722 | ||||||
| chr5:53623743 | G | A | 2 | a0002c0005t0002g0159 a0002c0005t0002g0160 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.177+20213G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623743 | |||||||
| chr5:53623749 | T | TC | 278 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.177+20221dupC | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53623749 | ||||||
| chr5:53623863 | C | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+20333C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623863 | |||||||
| chr5:53623933 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.177+20403A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53623933 | |||||||
| chr5:53624012 | C | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.177+20482C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624012 | |||||||
| chr5:53624013 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.177+20483G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624013 | |||||||
| chr5:53624088 | A | C | 2 | a0001c0002t0001g0007 a0001c0002t0001g0008 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.177+20558A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624088 | |||||||
| chr5:53624132 | A | G | 8 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0043 others(5): Show |
8 | HG01175.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+20602A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624132 | |||||||
| chr5:53624149 | T | C | 3 | a0001c0001t0001g0142 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG01167.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.177+20619T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624149 | |||||||
| chr5:53624215 | A | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.177+20685A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624215 | |||||||
| chr5:53624333 | T | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+20803T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624333 | |||||||
| chr5:53624401 | T | C | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.177+20871T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624401 | |||||||
| chr5:53624661 | A | G | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+21131A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624661 | |||||||
| chr5:53624689 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.177+21159A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624689 | |||||||
| chr5:53624784 | A | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+21254A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624784 | |||||||
| chr5:53624953 | G | A | 21 | a0001c0001t0002g0002 a0001c0001t0002g0176 a0001c0001t0002g0177 others(18): Show |
22 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.178-21280G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53624953 | |||||||
| chr5:53625094 | C | T | 3 | a0001c0002t0001g0066 a0001c0002t0001g0069 a0001c0002t0001g0082 |
3 | NA18970.hp2 NA18994.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.178-21139C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53625094 | |||||||
| chr5:53625144 | C | T | 1 | a0001c0004t0001g0020 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.178-21089C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53625144 | |||||||
| chr5:53625354 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.178-20879A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53625354 | |||||||
| chr5:53625623 | G | A | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.178-20610G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53625623 | |||||||
| chr5:53625659 | T | C | 2 | a0001c0002t0001g0048 a0001c0002t0001g0050 |
2 | HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.178-20574T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53625659 | |||||||
| chr5:53625741 | A | C | 287 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(284): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.178-20492A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53625741 | |||||||
| chr5:53625746 | C | CA | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.178-20486dupA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53625746 | ||||||
| chr5:53626105 | C | T | 1 | a0001c0001t0002g0212 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.178-20128C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53626105 | |||||||
| chr5:53626326 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.178-19907G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53626326 | |||||||
| chr5:53626370 | A | G | 1 | a0001c0001t0001g0357 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.178-19863A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53626370 | |||||||
| chr5:53626404 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.178-19829G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53626404 | |||||||
| chr5:53626824 | C | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.178-19409C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53626824 | |||||||
| chr5:53626904 | A | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.178-19329A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53626904 | |||||||
| chr5:53627021 | AC | A | 146 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.178-19211delC | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627021 | |||||||
| chr5:53627154 | G | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.178-19079G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627154 | |||||||
| chr5:53627215 | C | T | 1 | a0001c0003t0002g0140 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.178-19018C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627215 | |||||||
| chr5:53627376 | T | C | 1 | a0001c0004t0001g0086 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.178-18857T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627376 | |||||||
| chr5:53627405 | G | C | 44 | a0001c0003t0002g0001 a0001c0003t0002g0099 a0001c0003t0002g0100 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.178-18828G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627405 | |||||||
| chr5:53627421 | G | A | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.178-18812G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627421 | |||||||
| chr5:53627424 | A | G | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-18809A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627424 | |||||||
| chr5:53627475 | A | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.178-18758A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627475 | |||||||
| chr5:53627741 | G | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.178-18492G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627741 | |||||||
| chr5:53627753 | G | T | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.178-18480G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627753 | |||||||
| chr5:53627856 | A | G | 1 | a0001c0002t0001g0070 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.178-18377A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627856 | |||||||
| chr5:53627888 | G | A | 1 | a0001c0002t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.178-18345G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627888 | |||||||
| chr5:53627900 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.178-18333C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627900 | |||||||
| chr5:53627902 | G | C | 146 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.178-18331G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53627902 | |||||||
| chr5:53628066 | G | A | 2 | a0001c0002t0001g0157 a0001c0002t0001g0161 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.178-18167G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53628066 | |||||||
| chr5:53628231 | C | T | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.178-18002C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53628231 | |||||||
| chr5:53628354 | T | C | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.178-17879T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53628354 | |||||||
| chr5:53628414 | G | C | 146 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.178-17819G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53628414 | |||||||
| chr5:53628500 | C | T | 4 | a0001c0003t0002g0001 a0001c0003t0002g0103 a0001c0003t0002g0110 others(1): Show |
5 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-17733C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53628500 | |||||||
| chr5:53628968 | G | C | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.178-17265G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53628968 | |||||||
| chr5:53628997 | C | A | 7 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(4): Show |
7 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-17236C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53628997 | |||||||
| chr5:53629051 | T | C | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.178-17182T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53629051 | |||||||
| chr5:53629091 | C | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.178-17142C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53629091 | |||||||
| chr5:53629137 | C | T | 22 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0208 others(19): Show |
25 | HG01928.hp2 HG01934.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.178-17096C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53629137 | |||||||
| chr5:53629355 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.178-16878A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53629355 | |||||||
| chr5:53629736 | A | C | 2 | a0001c0003t0002g0227 a0001c0003t0002g0228 |
2 | NA18974.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.178-16497A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53629736 | |||||||
| chr5:53630188 | A | C | 3 | a0001c0003t0002g0136 a0001c0003t0002g0137 a0001c0003t0002g0138 |
3 | HG00673.hp2 HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.178-16045A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630188 | |||||||
| chr5:53630197 | G | A | 4 | a0001c0001t0002g0223 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | NA18959.hp1 NA18964.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-16036G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630197 | |||||||
| chr5:53630208 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.178-16025C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630208 | |||||||
| chr5:53630298 | T | C | 1 | a0001c0003t0002g0149 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.178-15935T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630298 | |||||||
| chr5:53630499 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-15734A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630499 | |||||||
| chr5:53630522 | A | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.178-15711A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630522 | |||||||
| chr5:53630542 | A | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.178-15691A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630542 | |||||||
| chr5:53630550 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.178-15683G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630550 | |||||||
| chr5:53630699 | G | A | 1 | a0001c0003t0002g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.178-15534G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630699 | |||||||
| chr5:53630829 | C | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.178-15404C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630829 | |||||||
| chr5:53630904 | C | T | 146 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.178-15329C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53630904 | |||||||
| chr5:53631094 | T | C | 1 | a0001c0004t0001g0012 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.178-15139T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631094 | |||||||
| chr5:53631129 | C | G | 1 | a0001c0004t0001g0014 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.178-15104C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631129 | |||||||
| chr5:53631207 | G | A | 8 | a0001c0004t0001g0084 a0001c0004t0001g0085 a0001c0004t0001g0086 others(5): Show |
8 | HG00609.hp1 NA18944.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-15026G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631207 | |||||||
| chr5:53631271 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.178-14962G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631271 | |||||||
| chr5:53631274 | A | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0275 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.178-14959A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631274 | |||||||
| chr5:53631318 | C | T | 16 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(13): Show |
16 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-14915C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631318 | |||||||
| chr5:53631319 | G | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.178-14914G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631319 | |||||||
| chr5:53631334 | G | T | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.178-14899G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631334 | |||||||
| chr5:53631347 | A | C | 1 | a0001c0001t0001g0313 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.178-14886A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631347 | |||||||
| chr5:53631457 | G | A | 3 | a0001c0001t0002g0211 a0001c0001t0002g0213 a0001c0001t0002g0214 |
3 | NA18973.hp2 NA19058.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.178-14776G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631457 | |||||||
| chr5:53631499 | C | G | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-14734C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631499 | |||||||
| chr5:53631531 | A | G | 2 | a0001c0002t0001g0157 a0001c0002t0001g0161 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.178-14702A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631531 | |||||||
| chr5:53631576 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-14657G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631576 | |||||||
| chr5:53631608 | A | G | 3 | a0001c0001t0001g0289 a0001c0001t0001g0326 a0001c0001t0001g0364 |
3 | NA18970.hp1 NA18979.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.178-14625A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631608 | |||||||
| chr5:53631712 | G | A | 4 | a0001c0001t0002g0146 a0001c0004t0001g0009 a0001c0004t0001g0016 others(1): Show |
4 | HG00558.hp1 HG02109.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-14521G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631712 | |||||||
| chr5:53631751 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.178-14482G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631751 | |||||||
| chr5:53631759 | A | C | 2 | a0001c0003t0002g0103 a0001c0003t0002g0111 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.178-14474A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631759 | |||||||
| chr5:53631767 | G | A | 146 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.178-14466G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631767 | |||||||
| chr5:53631808 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.178-14425T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631808 | |||||||
| chr5:53631868 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.178-14365G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631868 | |||||||
| chr5:53631881 | A | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.178-14352A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631881 | |||||||
| chr5:53631905 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.178-14328C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631905 | |||||||
| chr5:53631972 | C | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-14261C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631972 | |||||||
| chr5:53631983 | A | G | 278 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.178-14250A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631983 | |||||||
| chr5:53631992 | G | C | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.178-14241G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53631992 | |||||||
| chr5:53632054 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0256 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.178-14179G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53632054 | |||||||
| chr5:53632187 | T | A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0275 others(97): Show |
101 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.178-14046T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53632187 | |||||||
| chr5:53632202 | G | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.178-14031G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53632202 | |||||||
| chr5:53632249 | C | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0254 a0001c0001t0001g0255 |
3 | HG00140.hp1 HG01169.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.178-13984C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53632249 | |||||||
| chr5:53632332 | A | G | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.178-13901A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53632332 | |||||||
| chr5:53632433 | A | G | 1 | a0001c0001t0001g0360 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.178-13800A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53632433 | |||||||
| chr5:53632473 | A | G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.178-13760A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53632473 | |||||||
| chr5:53632562 | C | T | 146 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.178-13671C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53632562 | |||||||
| chr5:53632656 | T | A | 1 | a0001c0001t0002g0208 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.178-13577T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53632656 | |||||||
| chr5:53632966 | C | G | 1 | a0001c0001t0001g0367 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.178-13267C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53632966 | |||||||
| chr5:53633008 | G | C | 3 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02055.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.178-13225G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53633008 | |||||||
| chr5:53633052 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.178-13181G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53633052 | |||||||
| chr5:53633275 | A | C | 45 | a0001c0001t0002g0095 a0001c0003t0002g0001 a0001c0003t0002g0099 others(42): Show |
46 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.178-12958A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53633275 | |||||||
| chr5:53633395 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.178-12838T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53633395 | |||||||
| chr5:53633421 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.178-12812C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53633421 | |||||||
| chr5:53633629 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.178-12604A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53633629 | |||||||
| chr5:53633637 | T | C | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.178-12596T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53633637 | |||||||
| chr5:53633681 | G | C | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-12552G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53633681 | |||||||
| chr5:53633842 | C | G | 2 | a0001c0001t0002g0194 a0001c0001t0002g0205 |
2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.178-12391C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53633842 | |||||||
| chr5:53633966 | G | A | 132 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(129): Show |
133 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.178-12267G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53633966 | |||||||
| chr5:53634066 | T | G | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.178-12167T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53634066 | |||||||
| chr5:53634489 | T | C | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.178-11744T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53634489 | |||||||
| chr5:53634495 | C | G | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-11738C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53634495 | |||||||
| chr5:53634641 | G | A | 278 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.178-11592G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53634641 | |||||||
| chr5:53634678 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-11555T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53634678 | |||||||
| chr5:53634854 | C | A | 1 | a0001c0001t0002g0201 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.178-11379C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53634854 | |||||||
| chr5:53635093 | G | A | 11 | a0001c0003t0002g0119 a0001c0003t0002g0121 a0001c0003t0002g0124 others(8): Show |
11 | HG02155.hp2 NA18953.hp2 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.178-11140G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53635093 | |||||||
| chr5:53635187 | T | TTAAATAA others(1): Show |
26 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(23): Show |
26 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.178-11026_178-1101 others(12): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53635187 | ||||||
| chr5:53635187 | T | TTAAATAA others(5): Show |
3 | a0001c0001t0001g0142 a0001c0001t0001g0257 a0001c0001t0004g0269 |
3 | HG01167.hp1 HG03927.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-11030_178-1101 others(16): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53635187 | ||||||
| chr5:53635187 | T | TTAAATAA others(9): Show |
1 | a0001c0001t0001g0273 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178-11034_178-1101 others(20): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53635187 | ||||||
| chr5:53635212 | T | TAAATAAA others(13): Show |
1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.178-11019_178-1101 others(24): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53635212 | ||||||
| chr5:53635215 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.178-11018C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53635215 | |||||||
| chr5:53635309 | C | T | 1 | a0001c0003t0001g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.178-10924C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53635309 | |||||||
| chr5:53635348 | C | CA | 30 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(27): Show |
31 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.178-10872dupA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53635348 | ||||||
| chr5:53635369 | A | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-10864A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53635369 | |||||||
| chr5:53635421 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.178-10812G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53635421 | |||||||
| chr5:53635850 | T | A | 1 | a0001c0001t0001g0319 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.178-10383T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53635850 | |||||||
| chr5:53635896 | GTT | G | 132 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(129): Show |
133 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.178-10335_178-1033 others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53635896 | ||||||
| chr5:53635960 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.178-10273A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53635960 | |||||||
| chr5:53636290 | C | A | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.178-9943C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53636290 | |||||||
| chr5:53636375 | A | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.178-9858A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53636375 | |||||||
| chr5:53636684 | C | T | 1 | a0001c0001t0001g0371 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.178-9549C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53636684 | |||||||
| chr5:53636721 | T | A | 2 | a0001c0001t0001g0350 a0001c0001t0001g0351 |
2 | NA18982.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.178-9512T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53636721 | |||||||
| chr5:53637210 | CCA | C | 104 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(101): Show |
105 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.178-9022_178-9021d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637210 | |||||||
| chr5:53637214 | G | A | 104 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(101): Show |
105 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.178-9019G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637214 | |||||||
| chr5:53637230 | A | G | 278 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.178-9003A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637230 | |||||||
| chr5:53637231 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | NA19067.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.178-9002G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637231 | |||||||
| chr5:53637262 | C | A | 2 | a0001c0001t0001g0369 a0001c0001t0001g0370 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.178-8971C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637262 | |||||||
| chr5:53637335 | T | C | 1 | a0001c0001t0004g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.178-8898T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637335 | |||||||
| chr5:53637371 | A | G | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.178-8862A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637371 | |||||||
| chr5:53637633 | A | G | 4 | a0001c0002t0001g0055 a0001c0002t0001g0057 a0001c0002t0001g0073 others(1): Show |
4 | NA18956.hp1 NA18980.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-8600A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637633 | |||||||
| chr5:53637690 | A | C | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.178-8543A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637690 | |||||||
| chr5:53637715 | T | C | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.178-8518T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637715 | |||||||
| chr5:53637848 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.178-8385A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637848 | |||||||
| chr5:53637986 | G | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0302 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.178-8247G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53637986 | |||||||
| chr5:53638233 | T | C | 4 | a0001c0001t0002g0176 a0001c0001t0002g0190 a0001c0001t0002g0191 others(1): Show |
4 | HG01106.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-8000T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638233 | |||||||
| chr5:53638314 | C | A | 1 | a0001c0001t0002g0201 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.178-7919C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638314 | |||||||
| chr5:53638323 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.178-7910G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638323 | |||||||
| chr5:53638338 | T | G | 1 | a0001c0001t0002g0236 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.178-7895T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638338 | |||||||
| chr5:53638345 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.178-7888G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638345 | |||||||
| chr5:53638347 | A | C | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.178-7886A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638347 | |||||||
| chr5:53638439 | A | C | 1 | a0001c0001t0002g0241 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.178-7794A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638439 | |||||||
| chr5:53638575 | G | A | 247 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0272 others(244): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.178-7658G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638575 | |||||||
| chr5:53638603 | T | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-7630T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638603 | |||||||
| chr5:53638665 | A | G | 1 | a0001c0001t0001g0324 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.178-7568A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638665 | |||||||
| chr5:53638668 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-7565A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53638668 | |||||||
| chr5:53639037 | T | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-7196T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53639037 | |||||||
| chr5:53639044 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.178-7189G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53639044 | |||||||
| chr5:53639082 | ACT | A | 15 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(12): Show |
15 | HG01243.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-7146_178-7145d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53639082 | ||||||
| chr5:53639085 | C | G | 100 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0275 others(97): Show |
101 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.178-7148C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53639085 | |||||||
| chr5:53639217 | CTA | C | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.178-7004_178-7003d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53639217 | ||||||
| chr5:53639470 | T | G | 100 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0275 others(97): Show |
101 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.178-6763T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53639470 | |||||||
| chr5:53639566 | G | T | 13 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(10): Show |
13 | HG02027.hp1 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-6667G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53639566 | |||||||
| chr5:53639794 | T | C | 1 | a0001c0001t0001g0338 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-6439T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53639794 | |||||||
| chr5:53639800 | C | T | 1 | a0001c0001t0001g0338 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-6433C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53639800 | |||||||
| chr5:53639801 | T | C | 1 | a0001c0001t0001g0338 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-6432T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53639801 | |||||||
| chr5:53640026 | G | T | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.178-6207G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640026 | |||||||
| chr5:53640081 | GT | G | 16 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(13): Show |
16 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-6141delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53640081 | ||||||
| chr5:53640109 | C | T | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.178-6124C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640109 | |||||||
| chr5:53640192 | G | T | 16 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(13): Show |
16 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-6041G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640192 | |||||||
| chr5:53640198 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.178-6035T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640198 | |||||||
| chr5:53640215 | G | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-6018G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640215 | |||||||
| chr5:53640401 | G | A | 1 | a0001c0004t0001g0026 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.178-5832G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640401 | |||||||
| chr5:53640456 | G | C | 1 | a0001c0001t0001g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.178-5777G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640456 | |||||||
| chr5:53640533 | A | G | 332 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(329): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.178-5700A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640533 | |||||||
| chr5:53640652 | A | G | 2 | a0001c0001t0001g0324 a0001c0001t0001g0335 |
2 | NA18944.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.178-5581A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640652 | |||||||
| chr5:53640698 | A | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.178-5535A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640698 | |||||||
| chr5:53640708 | A | C | 295 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(292): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.178-5525A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640708 | |||||||
| chr5:53640807 | G | T | 1 | a0001c0007t0002g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178-5426G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640807 | |||||||
| chr5:53640834 | C | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-5399C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640834 | |||||||
| chr5:53640922 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.178-5311G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53640922 | |||||||
| chr5:53641066 | C | A | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.178-5167C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53641066 | |||||||
| chr5:53641164 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-5069A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53641164 | |||||||
| chr5:53641266 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.178-4967C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53641266 | |||||||
| chr5:53641527 | C | A | 1 | a0001c0001t0002g0229 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.178-4706C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53641527 | |||||||
| chr5:53641835 | T | G | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.178-4398T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53641835 | |||||||
| chr5:53641919 | G | A | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.178-4314G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53641919 | |||||||
| chr5:53641979 | G | T | 132 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(129): Show |
133 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.178-4254G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53641979 | |||||||
| chr5:53642007 | A | T | 104 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(101): Show |
105 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.178-4226A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53642007 | |||||||
| chr5:53642129 | T | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0257 |
2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.178-4104T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53642129 | |||||||
| chr5:53642441 | T | G | 2 | a0001c0004t0001g0013 a0001c0004t0001g0014 |
2 | HG01074.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.178-3792T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53642441 | |||||||
| chr5:53642763 | T | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.178-3470T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53642763 | |||||||
| chr5:53642874 | T | C | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.178-3359T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53642874 | |||||||
| chr5:53642962 | T | G | 10 | a0001c0003t0002g0119 a0001c0003t0002g0121 a0001c0003t0002g0124 others(7): Show |
10 | HG02155.hp2 NA18953.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-3271T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53642962 | |||||||
| chr5:53643130 | A | G | 4 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0363 others(1): Show |
4 | HG00609.hp2 NA18990.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-3103A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53643130 | |||||||
| chr5:53643202 | G | A | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.178-3031G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53643202 | |||||||
| chr5:53643418 | T | C | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-2815T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53643418 | |||||||
| chr5:53643446 | G | T | 1 | a0001c0001t0002g0202 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.178-2787G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53643446 | |||||||
| chr5:53643489 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.178-2744A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53643489 | |||||||
| chr5:53643573 | C | T | 1 | a0001c0001t0001g0361 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.178-2660C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53643573 | |||||||
| chr5:53643650 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.178-2583C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53643650 | |||||||
| chr5:53643852 | A | G | 1 | a0001c0001t0002g0180 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.178-2381A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53643852 | |||||||
| chr5:53643937 | G | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.178-2296G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53643937 | |||||||
| chr5:53644076 | A | G | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.178-2157A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53644076 | |||||||
| chr5:53644171 | T | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.178-2062T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53644171 | |||||||
| chr5:53644509 | G | A | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.178-1724G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53644509 | |||||||
| chr5:53644830 | G | A | 4 | a0001c0001t0002g0002 a0001c0001t0002g0186 a0001c0001t0002g0187 others(1): Show |
5 | HG01069.hp2 HG01071.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-1403G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53644830 | |||||||
| chr5:53644925 | T | A | 4 | a0001c0002t0001g0157 a0001c0002t0001g0161 a0001c0002t0001g0163 others(1): Show |
4 | HG01884.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-1308T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53644925 | |||||||
| chr5:53644984 | T | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.178-1249T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53644984 | |||||||
| chr5:53645014 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.178-1219G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645014 | |||||||
| chr5:53645034 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.178-1199C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645034 | |||||||
| chr5:53645061 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.178-1172G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645061 | |||||||
| chr5:53645092 | G | A | 1 | a0001c0001t0001g0363 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.178-1141G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645092 | |||||||
| chr5:53645194 | A | G | 1 | a0001c0001t0002g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.178-1039A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645194 | |||||||
| chr5:53645320 | A | T | 100 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0275 others(97): Show |
101 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.178-913A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645320 | |||||||
| chr5:53645349 | T | C | 4 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 others(1): Show |
4 | NA18942.hp2 NA18965.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-884T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645349 | |||||||
| chr5:53645417 | ACT | A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-813_178-812del others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 53645417 | ||||||
| chr5:53645455 | C | T | 1 | a0001c0001t0001g0362 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.178-778C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645455 | |||||||
| chr5:53645459 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.178-774G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645459 | |||||||
| chr5:53645667 | G | A | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-566G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645667 | |||||||
| chr5:53645711 | A | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.178-522A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645711 | |||||||
| chr5:53645888 | A | C | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-345A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645888 | |||||||
| chr5:53645892 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.178-341C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53645892 | |||||||
| chr5:53646005 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.178-228G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53646005 | |||||||
| chr5:53646029 | C | T | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-204C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53646029 | |||||||
| chr5:53646075 | A | G | 332 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(329): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.178-158A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53646075 | |||||||
| chr5:53646229 | G | C | 1 | a0001c0003t0002g0129 | 1 | NA19011.hp2 | splice_region_variant&intron_variant | LOW | c.178-4G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 2/4 | chr5 | 53646229 | |||||||
| chr5:53646411 | T | C | 1 | a0001c0001t0005g0349 | 1 | NA18999.hp1 | splice_region_variant&intron_variant | LOW | c.350+6T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53646411 | |||||||
| chr5:53646578 | TAA | T | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.350+174_350+175del others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53646578 | |||||||
| chr5:53646633 | C | T | 262 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.350+228C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53646633 | |||||||
| chr5:53646695 | T | TC | 100 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0275 others(97): Show |
101 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.350+296dupC | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53646695 | ||||||
| chr5:53646885 | G | A | 1 | a0001c0004t0001g0033 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.350+480G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53646885 | |||||||
| chr5:53646890 | A | G | 1 | a0001c0003t0002g0123 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.350+485A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53646890 | |||||||
| chr5:53646986 | T | A | 1 | a0001c0001t0002g0202 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.350+581T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53646986 | |||||||
| chr5:53646994 | C | T | 1 | a0001c0003t0002g0117 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.350+589C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53646994 | |||||||
| chr5:53646995 | C | G | 1 | a0001c0003t0002g0117 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.350+590C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53646995 | |||||||
| chr5:53647108 | G | A | 146 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.350+703G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647108 | |||||||
| chr5:53647116 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.350+711A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647116 | |||||||
| chr5:53647154 | T | G | 2 | a0001c0004t0001g0013 a0001c0004t0001g0014 |
2 | HG01074.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.350+749T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647154 | |||||||
| chr5:53647237 | T | G | 278 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.350+832T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647237 | |||||||
| chr5:53647254 | C | T | 1 | a0001c0001t0002g0210 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.350+849C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647254 | |||||||
| chr5:53647445 | G | A | 15 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(12): Show |
15 | HG01243.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.350+1040G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647445 | |||||||
| chr5:53647480 | G | A | 1 | a0001c0004t0001g0020 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.350+1075G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647480 | |||||||
| chr5:53647506 | C | T | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.350+1101C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647506 | |||||||
| chr5:53647605 | C | A | 15 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(12): Show |
15 | HG01243.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.350+1200C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647605 | |||||||
| chr5:53647672 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.350+1267A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647672 | |||||||
| chr5:53647696 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.350+1291G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647696 | |||||||
| chr5:53647723 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.350+1318C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647723 | |||||||
| chr5:53647756 | T | G | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.350+1351T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647756 | |||||||
| chr5:53647764 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.350+1359T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53647764 | |||||||
| chr5:53648005 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.350+1600T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648005 | |||||||
| chr5:53648025 | A | G | 1 | a0001c0001t0001g0371 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.350+1620A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648025 | |||||||
| chr5:53648030 | G | T | 1 | a0001c0004t0001g0037 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.350+1625G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648030 | |||||||
| chr5:53648190 | G | C | 1 | a0001c0001t0002g0202 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.350+1785G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648190 | |||||||
| chr5:53648202 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.350+1797A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648202 | |||||||
| chr5:53648208 | G | A | 1 | a0001c0004t0001g0087 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.350+1803G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648208 | |||||||
| chr5:53648589 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.350+2184A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648589 | |||||||
| chr5:53648598 | T | C | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.350+2193T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648598 | |||||||
| chr5:53648598 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.350+2193T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648598 | |||||||
| chr5:53648601 | A | G | 2 | a0001c0002t0001g0048 a0001c0002t0001g0050 |
2 | HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.350+2196A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648601 | |||||||
| chr5:53648849 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.350+2444T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648849 | |||||||
| chr5:53648889 | G | A | 279 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.350+2484G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648889 | |||||||
| chr5:53648922 | G | A | 1 | a0002c0005t0002g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.350+2517G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53648922 | |||||||
| chr5:53649028 | A | G | 1 | a0001c0002t0001g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.350+2623A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53649028 | |||||||
| chr5:53649118 | T | C | 278 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.350+2713T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53649118 | |||||||
| chr5:53649412 | C | T | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.350+3007C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53649412 | |||||||
| chr5:53649428 | T | C | 84 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(81): Show |
88 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.350+3023T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53649428 | |||||||
| chr5:53649555 | C | T | 29 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(26): Show |
29 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.350+3150C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53649555 | |||||||
| chr5:53649710 | A | G | 2 | a0001c0001t0002g0199 a0001c0001t0002g0203 |
2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.350+3305A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53649710 | |||||||
| chr5:53649818 | T | C | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.350+3413T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53649818 | |||||||
| chr5:53650028 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.350+3623G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650028 | |||||||
| chr5:53650062 | A | G | 4 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(1): Show |
4 | NA18939.hp2 NA18955.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.350+3657A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650062 | |||||||
| chr5:53650134 | T | A | 1 | a0001c0003t0002g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.350+3729T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650134 | |||||||
| chr5:53650199 | G | A | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.350+3794G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650199 | |||||||
| chr5:53650214 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.350+3809A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650214 | |||||||
| chr5:53650325 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.350+3920G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650325 | |||||||
| chr5:53650349 | A | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.350+3944A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650349 | |||||||
| chr5:53650368 | A | G | 15 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(12): Show |
15 | HG01243.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.350+3963A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650368 | |||||||
| chr5:53650373 | A | G | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | NA19010.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.350+3968A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650373 | |||||||
| chr5:53650628 | T | G | 1 | a0001c0001t0001g0303 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.350+4223T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650628 | |||||||
| chr5:53650782 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.350+4377G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650782 | |||||||
| chr5:53650843 | A | T | 2 | a0001c0003t0002g0099 a0001c0003t0002g0100 |
2 | HG01099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.350+4438A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53650843 | |||||||
| chr5:53651231 | A | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.350+4826A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651231 | |||||||
| chr5:53651236 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.350+4831G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651236 | |||||||
| chr5:53651257 | C | G | 1 | a0001c0001t0001g0321 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.350+4852C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651257 | |||||||
| chr5:53651278 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.350+4873G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651278 | |||||||
| chr5:53651304 | T | C | 1 | a0001c0003t0002g0117 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.350+4899T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651304 | |||||||
| chr5:53651531 | A | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.350+5126A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651531 | |||||||
| chr5:53651647 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.350+5242C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651647 | |||||||
| chr5:53651774 | C | CT | 18 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(15): Show |
18 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.350+5386dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53651774 | ||||||
| chr5:53651774 | CT | C | 257 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.350+5386delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53651774 | ||||||
| chr5:53651812 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.350+5407C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651812 | |||||||
| chr5:53651835 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.350+5430C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651835 | |||||||
| chr5:53651842 | G | A | 1 | a0001c0001t0001g0370 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.350+5437G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651842 | |||||||
| chr5:53651859 | G | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.350+5454G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651859 | |||||||
| chr5:53651866 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.350+5461G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651866 | |||||||
| chr5:53651974 | C | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.350+5569C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53651974 | |||||||
| chr5:53652056 | G | A | 261 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(258): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.350+5651G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53652056 | |||||||
| chr5:53652257 | G | GT | 6 | a0001c0001t0001g0285 a0001c0001t0002g0193 a0001c0001t0002g0204 others(3): Show |
6 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.350+5862dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53652257 | ||||||
| chr5:53652432 | TC | T | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.350+6028delC | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53652432 | |||||||
| chr5:53652608 | A | C | 1 | a0001c0001t0001g0332 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.351-5943A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53652608 | |||||||
| chr5:53652775 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.351-5776G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53652775 | |||||||
| chr5:53652938 | C | CT | 21 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(18): Show |
21 | HG01346.hp1 HG02055.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.351-5601dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53652938 | ||||||
| chr5:53653085 | A | C | 16 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(13): Show |
16 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.351-5466A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53653085 | |||||||
| chr5:53653153 | T | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.351-5398T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53653153 | |||||||
| chr5:53653154 | A | T | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.351-5397A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53653154 | |||||||
| chr5:53653160 | G | GT | 114 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(111): Show |
115 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.351-5383dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53653160 | ||||||
| chr5:53653160 | G | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.351-5391G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53653160 | |||||||
| chr5:53653228 | T | C | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.351-5323T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53653228 | |||||||
| chr5:53653479 | T | C | 1 | a0001c0001t0002g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.351-5072T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53653479 | |||||||
| chr5:53653655 | G | A | 1 | a0001c0002t0001g0008 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.351-4896G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53653655 | |||||||
| chr5:53653770 | G | A | 1 | a0001c0001t0001g0362 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.351-4781G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53653770 | |||||||
| chr5:53653978 | A | G | 1 | a0001c0001t0001g0358 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.351-4573A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53653978 | |||||||
| chr5:53654305 | T | C | 1 | a0001c0001t0001g0283 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.351-4246T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53654305 | |||||||
| chr5:53654480 | T | C | 13 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(10): Show |
13 | HG02109.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.351-4071T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53654480 | |||||||
| chr5:53654541 | C | T | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.351-4010C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53654541 | |||||||
| chr5:53654556 | A | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0254 a0001c0001t0001g0255 |
3 | HG00140.hp1 HG01169.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.351-3995A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53654556 | |||||||
| chr5:53654558 | A | G | 278 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.351-3993A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53654558 | |||||||
| chr5:53654604 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.351-3947C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53654604 | |||||||
| chr5:53654619 | G | C | 6 | a0001c0004t0001g0012 a0001c0004t0001g0034 a0001c0004t0001g0035 others(3): Show |
6 | NA18974.hp2 NA18982.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.351-3932G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53654619 | |||||||
| chr5:53655061 | A | AGTATAGT others(5): Show |
1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.351-3490_351-3489i others(14): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53655061 | |||||||
| chr5:53655062 | T | A | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.351-3489T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53655062 | |||||||
| chr5:53655063 | G | T | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.351-3488G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53655063 | |||||||
| chr5:53655162 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.351-3389A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53655162 | |||||||
| chr5:53655366 | AT | A | 21 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(18): Show |
21 | HG00558.hp2 HG01081.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.351-3166delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53655366 | ||||||
| chr5:53655423 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.351-3128C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53655423 | |||||||
| chr5:53655495 | CTG | C | 16 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(13): Show |
16 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.351-3054_351-3053d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53655495 | ||||||
| chr5:53655667 | A | C | 1 | a0001c0003t0002g0108 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.351-2884A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53655667 | |||||||
| chr5:53655699 | A | G | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.351-2852A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53655699 | |||||||
| chr5:53655865 | A | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.351-2686A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53655865 | |||||||
| chr5:53656077 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.351-2474G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53656077 | |||||||
| chr5:53656191 | A | G | 1 | a0001c0009t0001g0274 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351-2360A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53656191 | |||||||
| chr5:53656215 | A | AT | 273 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.351-2326dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53656215 | ||||||
| chr5:53656215 | A | T | 1 | a0001c0001t0002g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.351-2336A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53656215 | |||||||
| chr5:53656702 | G | C | 1 | a0001c0001t0002g0239 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.351-1849G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53656702 | |||||||
| chr5:53657104 | T | C | 1 | a0001c0001t0001g0368 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.351-1447T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657104 | |||||||
| chr5:53657218 | C | G | 98 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0275 others(95): Show |
99 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.351-1333C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657218 | |||||||
| chr5:53657240 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.351-1311C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657240 | |||||||
| chr5:53657289 | G | A | 141 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(138): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.351-1262G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657289 | |||||||
| chr5:53657316 | T | C | 6 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG02723.hp2 HG03225.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.351-1235T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657316 | |||||||
| chr5:53657320 | T | C | 1 | a0001c0001t0001g0326 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.351-1231T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657320 | |||||||
| chr5:53657374 | T | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(113): Show |
117 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.351-1177T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657374 | |||||||
| chr5:53657454 | C | T | 18 | a0001c0003t0002g0001 a0001c0003t0002g0099 a0001c0003t0002g0100 others(15): Show |
19 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.351-1097C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657454 | |||||||
| chr5:53657672 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.351-879A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657672 | |||||||
| chr5:53657903 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.351-648C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657903 | |||||||
| chr5:53657924 | CA | C | 19 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(16): Show |
19 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.351-609delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53657924 | ||||||
| chr5:53657924 | CAA | C | 112 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(109): Show |
113 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.351-610_351-609del others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 53657924 | ||||||
| chr5:53657934 | A | AC | 52 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(49): Show |
55 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.351-617_351-616ins others(1): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657934 | |||||||
| chr5:53657934 | A | C | 93 | a0001c0001t0002g0002 a0001c0001t0002g0095 a0001c0001t0002g0102 others(90): Show |
95 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.351-617A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53657934 | |||||||
| chr5:53658012 | G | C | 1 | a0001c0002t0001g0007 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.351-539G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53658012 | |||||||
| chr5:53658134 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.351-417A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53658134 | |||||||
| chr5:53658312 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.351-239A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53658312 | |||||||
| chr5:53658353 | A | G | 1 | a0001c0002t0001g0070 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.351-198A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53658353 | |||||||
| chr5:53658450 | G | A | 130 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(127): Show |
131 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.351-101G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53658450 | |||||||
| chr5:53658485 | A | C | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.351-66A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 3/4 | chr5 | 53658485 | |||||||
| chr5:53658638 | G | GT | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.424+19dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53658638 | ||||||
| chr5:53658684 | T | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0275 others(96): Show |
100 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.424+60T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53658684 | |||||||
| chr5:53658699 | A | G | 1 | a0001c0002t0001g0079 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.424+75A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53658699 | |||||||
| chr5:53658746 | G | T | 1 | a0001c0001t0001g0328 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.424+122G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53658746 | |||||||
| chr5:53658758 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.424+134T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53658758 | |||||||
| chr5:53658784 | C | CA | 150 | a0001c0001t0001g0142 a0001c0001t0001g0262 a0001c0001t0001g0263 others(147): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.424+180dupA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53658784 | ||||||
| chr5:53658784 | C | CAA | 117 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(114): Show |
118 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.424+179_424+180dup others(2): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53658784 | ||||||
| chr5:53658784 | C | CAAA | 11 | a0001c0001t0001g0266 a0001c0001t0001g0272 a0001c0001t0001g0273 others(8): Show |
11 | HG01106.hp1 HG01358.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+178_424+180dup others(3): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53658784 | ||||||
| chr5:53658920 | C | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+296C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53658920 | |||||||
| chr5:53658953 | T | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+329T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53658953 | |||||||
| chr5:53658989 | G | A | 18 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(15): Show |
18 | HG00140.hp1 HG01081.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+365G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53658989 | |||||||
| chr5:53659051 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.424+427A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53659051 | |||||||
| chr5:53659079 | GTAAAATT others(11): Show |
G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+460_424+477del others(18): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53659079 | ||||||
| chr5:53659186 | G | C | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+562G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53659186 | |||||||
| chr5:53659276 | T | C | 1 | a0001c0001t0002g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.424+652T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53659276 | |||||||
| chr5:53659293 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.424+669G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53659293 | |||||||
| chr5:53659322 | G | T | 1 | a0001c0002t0001g0064 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.424+698G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53659322 | |||||||
| chr5:53659724 | C | T | 283 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.424+1100C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53659724 | |||||||
| chr5:53659817 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.424+1193T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53659817 | |||||||
| chr5:53659930 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424+1306A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53659930 | |||||||
| chr5:53660005 | C | CT | 8 | a0001c0001t0002g0175 a0001c0001t0002g0194 a0001c0001t0002g0195 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+1390dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53660005 | ||||||
| chr5:53660005 | CT | C | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+1390delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53660005 | ||||||
| chr5:53660014 | T | A | 2 | a0001c0001t0001g0369 a0001c0001t0001g0370 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+1390T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660014 | |||||||
| chr5:53660101 | C | A | 1 | a0001c0001t0001g0371 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.424+1477C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660101 | |||||||
| chr5:53660107 | A | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+1483A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660107 | |||||||
| chr5:53660152 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.424+1528C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660152 | |||||||
| chr5:53660334 | C | A | 1 | a0001c0001t0001g0363 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.424+1710C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660334 | |||||||
| chr5:53660370 | G | T | 1 | a0001c0001t0002g0238 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.424+1746G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660370 | |||||||
| chr5:53660399 | T | C | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.424+1775T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660399 | |||||||
| chr5:53660503 | G | C | 1 | a0001c0001t0002g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.424+1879G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660503 | |||||||
| chr5:53660568 | T | C | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+1944T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660568 | |||||||
| chr5:53660657 | A | T | 1 | a0001c0001t0001g0292 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.424+2033A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660657 | |||||||
| chr5:53660701 | G | A | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.424+2077G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660701 | |||||||
| chr5:53660802 | T | G | 98 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(95): Show |
99 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.424+2178T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660802 | |||||||
| chr5:53660826 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+2202C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53660826 | |||||||
| chr5:53661020 | C | G | 5 | a0001c0002t0001g0066 a0001c0002t0001g0068 a0001c0002t0001g0069 others(2): Show |
5 | NA18970.hp2 NA18994.hp2 NA19087.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2396C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661020 | |||||||
| chr5:53661082 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.424+2458A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661082 | |||||||
| chr5:53661194 | G | T | 1 | a0001c0004t0001g0018 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.424+2570G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661194 | |||||||
| chr5:53661246 | C | A | 5 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0002g0146 others(2): Show |
5 | HG01256.hp2 HG01258.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2622C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661246 | |||||||
| chr5:53661246 | C | G | 1 | a0001c0002t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.424+2622C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661246 | |||||||
| chr5:53661252 | T | G | 1 | a0001c0002t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.424+2628T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661252 | |||||||
| chr5:53661272 | G | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0348 |
2 | HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.424+2648G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661272 | |||||||
| chr5:53661300 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+2676C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661300 | |||||||
| chr5:53661356 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.424+2732G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661356 | |||||||
| chr5:53661394 | G | T | 1 | a0001c0001t0001g0292 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.424+2770G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661394 | |||||||
| chr5:53661433 | T | A | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+2809T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661433 | |||||||
| chr5:53661439 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.424+2815C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661439 | |||||||
| chr5:53661475 | G | A | 2 | a0001c0001t0002g0188 a0001c0001t0002g0206 |
2 | HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.424+2851G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661475 | |||||||
| chr5:53661481 | C | T | 1 | a0001c0003t0001g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.424+2857C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661481 | |||||||
| chr5:53661485 | C | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+2861C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661485 | |||||||
| chr5:53661504 | G | T | 260 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(257): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.424+2880G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661504 | |||||||
| chr5:53661507 | G | C | 260 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(257): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.424+2883G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661507 | |||||||
| chr5:53661517 | G | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0172 |
2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.424+2893G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661517 | |||||||
| chr5:53661559 | G | C | 1 | a0001c0001t0001g0310 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.424+2935G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661559 | |||||||
| chr5:53661664 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.424+3040G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661664 | |||||||
| chr5:53661676 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.424+3052T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661676 | |||||||
| chr5:53661693 | G | T | 4 | a0001c0002t0001g0157 a0001c0002t0001g0161 a0001c0002t0001g0163 others(1): Show |
4 | HG01884.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+3069G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661693 | |||||||
| chr5:53661727 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.424+3103G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661727 | |||||||
| chr5:53661795 | G | GCTGT | 276 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(273): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.424+3176_424+3179d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53661795 | ||||||
| chr5:53661822 | C | G | 1 | a0001c0003t0002g0126 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.424+3198C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661822 | |||||||
| chr5:53661829 | T | G | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.424+3205T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661829 | |||||||
| chr5:53661951 | AT | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(110): Show |
114 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.424+3330delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53661951 | ||||||
| chr5:53661981 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+3357C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53661981 | |||||||
| chr5:53662013 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+3389G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662013 | |||||||
| chr5:53662114 | T | G | 1 | a0001c0003t0002g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.424+3490T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662114 | |||||||
| chr5:53662244 | A | G | 1 | a0001c0003t0002g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.424+3620A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662244 | |||||||
| chr5:53662247 | C | G | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+3623C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662247 | |||||||
| chr5:53662451 | A | C | 15 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(12): Show |
15 | HG01243.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.424+3827A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662451 | |||||||
| chr5:53662517 | G | C | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+3893G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662517 | |||||||
| chr5:53662542 | A | G | 6 | a0001c0002t0001g0056 a0001c0002t0001g0058 a0001c0002t0001g0062 others(3): Show |
6 | HG02738.hp2 HG03669.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+3918A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662542 | |||||||
| chr5:53662603 | C | T | 2 | a0001c0002t0001g0157 a0001c0002t0001g0161 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.424+3979C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662603 | |||||||
| chr5:53662611 | A | T | 1 | a0001c0001t0001g0303 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.424+3987A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662611 | |||||||
| chr5:53662646 | T | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(112): Show |
116 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.424+4022T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662646 | |||||||
| chr5:53662662 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424+4038T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662662 | |||||||
| chr5:53662720 | T | C | 1 | a0001c0004t0001g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.424+4096T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662720 | |||||||
| chr5:53662727 | G | A | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.424+4103G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662727 | |||||||
| chr5:53662735 | T | C | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.424+4111T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662735 | |||||||
| chr5:53662771 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.424+4147A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662771 | |||||||
| chr5:53662781 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.424+4157A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662781 | |||||||
| chr5:53662796 | GTA | G | 259 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(256): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.424+4176_424+4177d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53662796 | ||||||
| chr5:53662816 | T | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+4192T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662816 | |||||||
| chr5:53662822 | C | G | 4 | a0001c0001t0002g0176 a0001c0001t0002g0190 a0001c0001t0002g0191 others(1): Show |
4 | HG01106.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+4198C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662822 | |||||||
| chr5:53662824 | G | C | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+4200G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662824 | |||||||
| chr5:53662930 | A | C | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4306A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662930 | |||||||
| chr5:53662965 | A | G | 1 | a0001c0009t0001g0274 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.424+4341A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662965 | |||||||
| chr5:53662974 | C | A | 8 | a0001c0004t0001g0084 a0001c0004t0001g0085 a0001c0004t0001g0086 others(5): Show |
8 | HG00609.hp1 NA18944.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+4350C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53662974 | |||||||
| chr5:53663162 | T | G | 1 | a0001c0009t0001g0274 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.424+4538T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53663162 | |||||||
| chr5:53663180 | T | G | 277 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.424+4556T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53663180 | |||||||
| chr5:53663313 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.424+4689T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53663313 | |||||||
| chr5:53663464 | CT | C | 7 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0342 others(4): Show |
7 | HG00438.hp1 HG02056.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+4842delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53663464 | ||||||
| chr5:53663505 | T | C | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+4881T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53663505 | |||||||
| chr5:53663864 | A | T | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.424+5240A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53663864 | |||||||
| chr5:53663882 | C | T | 130 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(127): Show |
131 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.424+5258C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53663882 | |||||||
| chr5:53663942 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.424+5318A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53663942 | |||||||
| chr5:53663949 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+5325A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53663949 | |||||||
| chr5:53663970 | CTTG | C | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+5352_424+5354d others(5): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53663970 | ||||||
| chr5:53664025 | C | G | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.424+5401C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664025 | |||||||
| chr5:53664173 | G | A | 84 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(81): Show |
88 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.424+5549G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664173 | |||||||
| chr5:53664199 | A | T | 1 | a0001c0004t0001g0026 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.424+5575A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664199 | |||||||
| chr5:53664257 | G | A | 1 | a0001c0004t0001g0036 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.424+5633G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664257 | |||||||
| chr5:53664265 | C | T | 130 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(127): Show |
131 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.424+5641C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664265 | |||||||
| chr5:53664297 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.424+5673C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664297 | |||||||
| chr5:53664392 | G | A | 53 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(50): Show |
56 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.424+5768G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664392 | |||||||
| chr5:53664570 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424+5946T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664570 | |||||||
| chr5:53664593 | A | G | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.424+5969A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664593 | |||||||
| chr5:53664640 | G | T | 1 | a0001c0002t0001g0060 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.424+6016G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664640 | |||||||
| chr5:53664650 | C | T | 1 | a0001c0002t0001g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.424+6026C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664650 | |||||||
| chr5:53664775 | A | C | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.424+6151A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664775 | |||||||
| chr5:53664793 | G | A | 1 | a0001c0001t0001g0330 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.424+6169G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664793 | |||||||
| chr5:53664815 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424+6191C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664815 | |||||||
| chr5:53664828 | C | T | 39 | a0001c0001t0001g0288 a0001c0001t0001g0322 a0001c0002t0001g0040 others(36): Show |
39 | HG00323.hp1 HG00639.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.424+6204C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664828 | |||||||
| chr5:53664901 | G | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+6277G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53664901 | |||||||
| chr5:53665087 | G | A | 2 | a0001c0002t0001g0157 a0001c0002t0001g0161 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.424+6463G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665087 | |||||||
| chr5:53665337 | C | G | 4 | a0001c0001t0001g0361 a0001c0001t0001g0362 a0001c0001t0001g0363 others(1): Show |
4 | HG00609.hp2 NA18990.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6713C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665337 | |||||||
| chr5:53665461 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+6837C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665461 | |||||||
| chr5:53665535 | C | A | 1 | a0001c0001t0002g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.424+6911C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665535 | |||||||
| chr5:53665594 | C | T | 146 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.424+6970C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665594 | |||||||
| chr5:53665650 | G | T | 1 | a0001c0001t0001g0361 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.424+7026G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665650 | |||||||
| chr5:53665668 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+7044G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665668 | |||||||
| chr5:53665746 | A | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+7122A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665746 | |||||||
| chr5:53665813 | G | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+7189G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665813 | |||||||
| chr5:53665920 | C | T | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+7296C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665920 | |||||||
| chr5:53665921 | G | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+7297G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665921 | |||||||
| chr5:53665962 | T | A | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | NA18983.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.424+7338T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53665962 | |||||||
| chr5:53666003 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.424+7379A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666003 | |||||||
| chr5:53666144 | A | G | 2 | a0001c0002t0001g0157 a0001c0002t0001g0161 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.424+7520A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666144 | |||||||
| chr5:53666151 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0256 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.424+7527T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666151 | |||||||
| chr5:53666237 | T | C | 1 | a0001c0001t0002g0102 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.424+7613T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666237 | |||||||
| chr5:53666408 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.424+7784C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666408 | |||||||
| chr5:53666409 | C | T | 2 | a0001c0001t0001g0367 a0001c0001t0001g0368 |
2 | HG00639.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.424+7785C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666409 | |||||||
| chr5:53666421 | C | T | 283 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.424+7797C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666421 | |||||||
| chr5:53666429 | C | T | 7 | a0001c0001t0002g0175 a0001c0001t0002g0194 a0001c0001t0002g0195 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+7805C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666429 | |||||||
| chr5:53666651 | TCTGA | T | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.424+8031_424+8034d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53666651 | ||||||
| chr5:53666805 | G | A | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.424+8181G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666805 | |||||||
| chr5:53666839 | C | T | 1 | a0001c0001t0001g0371 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.424+8215C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666839 | |||||||
| chr5:53666974 | T | G | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+8350T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53666974 | |||||||
| chr5:53667043 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.424+8419G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667043 | |||||||
| chr5:53667177 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.424+8553G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667177 | |||||||
| chr5:53667191 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424+8567C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667191 | |||||||
| chr5:53667194 | G | A | 32 | a0001c0001t0001g0168 a0001c0001t0002g0002 a0001c0001t0002g0175 others(29): Show |
33 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+8570G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667194 | |||||||
| chr5:53667204 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.424+8580G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667204 | |||||||
| chr5:53667207 | T | G | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.424+8583T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667207 | |||||||
| chr5:53667220 | C | T | 1 | a0001c0001t0002g0223 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.424+8596C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667220 | |||||||
| chr5:53667241 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.424+8617G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667241 | |||||||
| chr5:53667321 | C | T | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.424+8697C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667321 | |||||||
| chr5:53667351 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+8727G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667351 | |||||||
| chr5:53667380 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.424+8756G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667380 | |||||||
| chr5:53667389 | C | T | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.424+8765C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667389 | |||||||
| chr5:53667486 | CA | C | 143 | a0001c0001t0001g0142 a0001c0001t0002g0002 a0001c0001t0002g0003 others(140): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.424+8879delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53667486 | ||||||
| chr5:53667486 | CAA | C | 18 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(15): Show |
18 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+8878_424+8879d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53667486 | ||||||
| chr5:53667486 | CAAA | C | 112 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(109): Show |
113 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.424+8877_424+8879d others(5): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53667486 | ||||||
| chr5:53667517 | G | A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.424+8893G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667517 | |||||||
| chr5:53667555 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.424+8931C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667555 | |||||||
| chr5:53667643 | A | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+9019A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667643 | |||||||
| chr5:53667937 | C | A | 2 | a0001c0001t0002g0211 a0001c0001t0002g0214 |
2 | NA19058.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.424+9313C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667937 | |||||||
| chr5:53667952 | C | T | 1 | a0002c0005t0002g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.424+9328C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53667952 | |||||||
| chr5:53668074 | C | G | 2 | a0001c0001t0001g0369 a0001c0001t0001g0370 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+9450C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53668074 | |||||||
| chr5:53668203 | G | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG02723.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.424+9579G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53668203 | |||||||
| chr5:53668235 | A | G | 114 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(111): Show |
115 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.424+9611A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53668235 | |||||||
| chr5:53668454 | T | G | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.424+9830T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53668454 | |||||||
| chr5:53668512 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.424+9888G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53668512 | |||||||
| chr5:53668595 | A | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+9971A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53668595 | |||||||
| chr5:53668616 | A | AT | 15 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0287 others(12): Show |
15 | HG01891.hp1 HG01891.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.424+10014dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53668616 | ||||||
| chr5:53668616 | AT | A | 63 | a0001c0001t0001g0142 a0001c0001t0001g0271 a0001c0001t0001g0302 others(60): Show |
66 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.424+10014delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53668616 | ||||||
| chr5:53668616 | ATT | A | 21 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0255 others(18): Show |
21 | HG01099.hp1 HG01169.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+10013_424+1001 others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53668616 | ||||||
| chr5:53668911 | G | T | 22 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0208 others(19): Show |
25 | HG01928.hp2 HG01934.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.424+10287G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53668911 | |||||||
| chr5:53668927 | T | G | 1 | a0001c0003t0002g0135 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.424+10303T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53668927 | |||||||
| chr5:53669170 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.424+10546C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53669170 | |||||||
| chr5:53669306 | A | C | 52 | a0001c0001t0001g0271 a0001c0001t0002g0003 a0001c0001t0002g0004 others(49): Show |
55 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.424+10682A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53669306 | |||||||
| chr5:53669308 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+10684T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53669308 | |||||||
| chr5:53669401 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.424+10777G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53669401 | |||||||
| chr5:53669440 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.424+10816C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53669440 | |||||||
| chr5:53669589 | A | G | 1 | a0001c0003t0002g0126 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.424+10965A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53669589 | |||||||
| chr5:53669707 | C | G | 1 | a0001c0001t0002g0098 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.424+11083C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53669707 | |||||||
| chr5:53669744 | G | A | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.424+11120G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53669744 | |||||||
| chr5:53669761 | A | G | 1 | a0001c0001t0002g0002 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.424+11137A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53669761 | |||||||
| chr5:53669889 | T | A | 1 | a0001c0001t0001g0372 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.424+11265T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53669889 | |||||||
| chr5:53669901 | C | CT | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+11284dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53669901 | ||||||
| chr5:53670097 | C | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.424+11473C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670097 | |||||||
| chr5:53670130 | C | T | 5 | a0001c0003t0002g0112 a0001c0003t0002g0113 a0001c0003t0002g0114 others(2): Show |
5 | NA18964.hp1 NA18999.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+11506C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670130 | |||||||
| chr5:53670434 | GA | G | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+11820delA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53670434 | ||||||
| chr5:53670450 | T | C | 1 | a0001c0004t0001g0087 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.424+11826T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670450 | |||||||
| chr5:53670529 | CTTTTA | C | 89 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(86): Show |
90 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.424+11909_424+1191 others(9): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53670529 | ||||||
| chr5:53670621 | T | TTA | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.424+12013_424+1201 others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53670621 | ||||||
| chr5:53670700 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.424+12076C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670700 | |||||||
| chr5:53670727 | C | T | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.424+12103C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670727 | |||||||
| chr5:53670748 | A | G | 1 | a0001c0001t0001g0326 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.424+12124A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670748 | |||||||
| chr5:53670809 | T | A | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424+12185T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670809 | |||||||
| chr5:53670826 | A | G | 1 | a0001c0003t0002g0125 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.424+12202A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670826 | |||||||
| chr5:53670875 | G | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.425-12243G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670875 | |||||||
| chr5:53670923 | A | T | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.425-12195A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670923 | |||||||
| chr5:53670953 | A | G | 2 | a0001c0004t0001g0011 a0001c0004t0001g0018 |
2 | HG02293.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.425-12165A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670953 | |||||||
| chr5:53670987 | A | G | 1 | a0001c0002t0001g0008 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.425-12131A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670987 | |||||||
| chr5:53670994 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.425-12124G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53670994 | |||||||
| chr5:53671184 | G | A | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.425-11934G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53671184 | |||||||
| chr5:53671196 | T | C | 4 | a0001c0001t0001g0290 a0001c0001t0001g0317 a0001c0001t0001g0324 others(1): Show |
4 | NA18944.hp2 NA18956.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-11922T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53671196 | |||||||
| chr5:53671275 | C | T | 1 | a0001c0007t0002g0178 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.425-11843C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53671275 | |||||||
| chr5:53671375 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.425-11743C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53671375 | |||||||
| chr5:53671459 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.425-11659C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53671459 | |||||||
| chr5:53671750 | G | T | 3 | a0001c0001t0001g0329 a0001c0001t0001g0336 a0001c0001t0001g0340 |
3 | NA18986.hp2 NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.425-11368G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53671750 | |||||||
| chr5:53671824 | T | C | 15 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(12): Show |
15 | HG01243.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.425-11294T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53671824 | |||||||
| chr5:53671896 | CATT | C | 3 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0001g0344 |
3 | NA18948.hp1 NA18960.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.425-11221_425-1121 others(7): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53671896 | |||||||
| chr5:53672050 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.425-11068G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53672050 | |||||||
| chr5:53672053 | C | T | 31 | a0001c0001t0002g0002 a0001c0001t0002g0175 a0001c0001t0002g0176 others(28): Show |
32 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.425-11065C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53672053 | |||||||
| chr5:53672112 | G | A | 1 | a0001c0003t0002g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.425-11006G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53672112 | |||||||
| chr5:53672137 | A | G | 98 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(95): Show |
99 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.425-10981A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53672137 | |||||||
| chr5:53672141 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.425-10977G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53672141 | |||||||
| chr5:53672219 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.425-10899T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53672219 | |||||||
| chr5:53672433 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.425-10685T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53672433 | |||||||
| chr5:53672490 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.425-10628A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53672490 | |||||||
| chr5:53672605 | GT | G | 255 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(252): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.425-10503delT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53672605 | ||||||
| chr5:53673104 | G | A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.425-10014G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53673104 | |||||||
| chr5:53673303 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.425-9815C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53673303 | |||||||
| chr5:53673343 | C | T | 1 | a0001c0003t0002g0123 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.425-9775C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53673343 | |||||||
| chr5:53673357 | C | T | 5 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0001c0001t0001g0280 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.425-9761C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53673357 | |||||||
| chr5:53673377 | A | G | 7 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(4): Show |
7 | HG02027.hp2 HG02723.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-9741A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53673377 | |||||||
| chr5:53673603 | T | C | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-9515T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53673603 | |||||||
| chr5:53673638 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.425-9480A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53673638 | |||||||
| chr5:53673653 | A | G | 2 | a0001c0003t0002g0112 a0001c0003t0002g0113 |
2 | NA19007.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.425-9465A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53673653 | |||||||
| chr5:53673666 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.425-9452C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53673666 | |||||||
| chr5:53673931 | C | A | 1 | a0001c0001t0001g0366 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.425-9187C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53673931 | |||||||
| chr5:53674115 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.425-9003C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53674115 | |||||||
| chr5:53674147 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.425-8971A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53674147 | |||||||
| chr5:53674202 | T | G | 18 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(15): Show |
18 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.425-8916T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53674202 | |||||||
| chr5:53674241 | A | G | 7 | a0001c0002t0001g0008 a0001c0002t0001g0041 a0001c0002t0001g0043 others(4): Show |
7 | HG02055.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.425-8877A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53674241 | |||||||
| chr5:53674465 | G | A | 2 | a0001c0003t0002g0112 a0001c0003t0002g0113 |
2 | NA19007.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.425-8653G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53674465 | |||||||
| chr5:53674494 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.425-8624A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53674494 | |||||||
| chr5:53674509 | G | A | 283 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.425-8609G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53674509 | |||||||
| chr5:53674620 | T | G | 2 | a0001c0002t0001g0157 a0001c0002t0001g0161 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.425-8498T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53674620 | |||||||
| chr5:53675157 | C | CT | 144 | a0001c0001t0001g0168 a0001c0001t0001g0275 a0001c0001t0001g0276 others(141): Show |
147 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.425-7939dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53675157 | ||||||
| chr5:53675157 | C | CTT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0280 others(20): Show |
24 | HG00423.hp2 HG01167.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.425-7940_425-7939d others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53675157 | ||||||
| chr5:53675192 | C | T | 50 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(47): Show |
53 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.425-7926C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675192 | |||||||
| chr5:53675193 | A | G | 50 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(47): Show |
53 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.425-7925A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675193 | |||||||
| chr5:53675241 | C | CA | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.425-7875dupA | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53675241 | ||||||
| chr5:53675317 | C | T | 2 | a0001c0001t0002g0190 a0001c0001t0002g0191 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.425-7801C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675317 | |||||||
| chr5:53675319 | C | T | 2 | a0001c0003t0002g0135 a0001c0003t0002g0228 |
2 | NA18953.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.425-7799C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675319 | |||||||
| chr5:53675379 | T | G | 285 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(282): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.425-7739T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675379 | |||||||
| chr5:53675387 | T | C | 1 | a0001c0001t0001g0371 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.425-7731T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675387 | |||||||
| chr5:53675428 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.425-7690C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675428 | |||||||
| chr5:53675436 | A | G | 96 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(93): Show |
97 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.425-7682A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675436 | |||||||
| chr5:53675529 | C | CGTGT | 8 | a0001c0002t0001g0008 a0001c0002t0001g0041 a0001c0002t0001g0042 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-7588_425-7587i others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53675529 | ||||||
| chr5:53675529 | C | T | 6 | a0001c0003t0002g0112 a0001c0003t0002g0113 a0001c0003t0002g0114 others(3): Show |
6 | HG03239.hp1 NA18964.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-7589C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675529 | |||||||
| chr5:53675583 | G | A | 111 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(108): Show |
112 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.425-7535G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675583 | |||||||
| chr5:53675888 | G | A | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | NA19010.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.425-7230G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675888 | |||||||
| chr5:53675969 | T | C | 15 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(12): Show |
15 | HG01243.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.425-7149T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53675969 | |||||||
| chr5:53676163 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.425-6955T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676163 | |||||||
| chr5:53676208 | G | A | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.425-6910G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676208 | |||||||
| chr5:53676251 | G | A | 45 | a0001c0001t0002g0095 a0001c0003t0002g0001 a0001c0003t0002g0099 others(42): Show |
46 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.425-6867G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676251 | |||||||
| chr5:53676391 | G | A | 258 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(255): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.425-6727G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676391 | |||||||
| chr5:53676562 | T | G | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-6556T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676562 | |||||||
| chr5:53676667 | G | A | 7 | a0001c0001t0004g0269 a0001c0002t0001g0157 a0001c0002t0001g0161 others(4): Show |
7 | HG01884.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-6451G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676667 | |||||||
| chr5:53676739 | C | T | 6 | a0001c0002t0001g0157 a0001c0002t0001g0161 a0001c0002t0001g0163 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-6379C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676739 | |||||||
| chr5:53676800 | A | T | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.425-6318A>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676800 | |||||||
| chr5:53676829 | C | T | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.425-6289C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676829 | |||||||
| chr5:53676839 | T | C | 283 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.425-6279T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676839 | |||||||
| chr5:53676840 | G | A | 1 | a0001c0001t0001g0361 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.425-6278G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676840 | |||||||
| chr5:53676845 | A | AT | 21 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(18): Show |
21 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.425-6263dupT | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53676845 | ||||||
| chr5:53676913 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.425-6205G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53676913 | |||||||
| chr5:53677094 | G | A | 119 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0251 others(116): Show |
120 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.425-6024G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53677094 | |||||||
| chr5:53677098 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.425-6020A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53677098 | |||||||
| chr5:53677291 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.425-5827T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53677291 | |||||||
| chr5:53677399 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.425-5719A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53677399 | |||||||
| chr5:53677426 | T | C | 39 | a0001c0001t0001g0288 a0001c0001t0001g0322 a0001c0002t0001g0040 others(36): Show |
39 | HG00323.hp1 HG00639.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.425-5692T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53677426 | |||||||
| chr5:53677453 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.425-5665A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53677453 | |||||||
| chr5:53677508 | C | T | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.425-5610C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53677508 | |||||||
| chr5:53677792 | A | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.425-5326A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53677792 | |||||||
| chr5:53677980 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.425-5138T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53677980 | |||||||
| chr5:53678172 | GGAGATCT others(29): Show |
G | 1 | a0001c0001t0002g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.425-4943_425-4908d others(38): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53678172 | ||||||
| chr5:53678270 | A | C | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-4848A>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678270 | |||||||
| chr5:53678345 | C | T | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.425-4773C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678345 | |||||||
| chr5:53678410 | C | G | 1 | a0001c0002t0001g0081 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.425-4708C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678410 | |||||||
| chr5:53678422 | G | A | 1 | a0001c0003t0002g0136 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.425-4696G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678422 | |||||||
| chr5:53678425 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-4693G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678425 | |||||||
| chr5:53678514 | A | G | 2 | a0001c0004t0001g0026 a0001c0004t0001g0039 |
2 | NA18983.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.425-4604A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678514 | |||||||
| chr5:53678567 | T | C | 1 | a0001c0003t0002g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.425-4551T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678567 | |||||||
| chr5:53678739 | C | A | 1 | a0001c0002t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.425-4379C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678739 | |||||||
| chr5:53678793 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.425-4325G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678793 | |||||||
| chr5:53678804 | G | A | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.425-4314G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678804 | |||||||
| chr5:53678810 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.425-4308C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678810 | |||||||
| chr5:53678811 | T | G | 112 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(109): Show |
113 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.425-4307T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53678811 | |||||||
| chr5:53679239 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.425-3879A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53679239 | |||||||
| chr5:53679337 | CTGTG | C | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.425-3779_425-3776d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53679337 | ||||||
| chr5:53679709 | A | G | 2 | a0001c0003t0002g0137 a0001c0003t0002g0138 |
2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.425-3409A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53679709 | |||||||
| chr5:53679900 | A | G | 98 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(95): Show |
99 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.425-3218A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53679900 | |||||||
| chr5:53680045 | C | T | 4 | a0001c0001t0001g0360 a0001c0002t0001g0040 a0001c0002t0001g0054 others(1): Show |
4 | HG03942.hp1 NA18959.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-3073C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680045 | |||||||
| chr5:53680148 | T | C | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.425-2970T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680148 | |||||||
| chr5:53680154 | G | GTTTA | 90 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(87): Show |
91 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.425-2960_425-2957d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53680154 | ||||||
| chr5:53680166 | G | A | 13 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0145 others(10): Show |
13 | HG02109.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.425-2952G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680166 | |||||||
| chr5:53680185 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.425-2933T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680185 | |||||||
| chr5:53680372 | G | T | 1 | a0001c0001t0001g0334 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.425-2746G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680372 | |||||||
| chr5:53680452 | A | G | 4 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(1): Show |
4 | NA18942.hp1 NA18951.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2666A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680452 | |||||||
| chr5:53680516 | A | G | 53 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(50): Show |
56 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.425-2602A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680516 | |||||||
| chr5:53680525 | T | A | 277 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.425-2593T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680525 | |||||||
| chr5:53680548 | A | G | 3 | a0001c0004t0001g0084 a0001c0004t0001g0085 a0001c0004t0001g0087 |
3 | NA18979.hp1 NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.425-2570A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680548 | |||||||
| chr5:53680589 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-2529G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680589 | |||||||
| chr5:53680709 | C | T | 18 | a0001c0003t0002g0001 a0001c0003t0002g0099 a0001c0003t0002g0100 others(15): Show |
19 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.425-2409C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680709 | |||||||
| chr5:53680711 | G | C | 7 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0342 others(4): Show |
7 | HG00438.hp1 HG02056.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-2407G>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680711 | |||||||
| chr5:53680761 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.425-2357G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680761 | |||||||
| chr5:53680764 | G | A | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.425-2354G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680764 | |||||||
| chr5:53680870 | C | G | 1 | a0001c0004t0001g0018 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.425-2248C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680870 | |||||||
| chr5:53680907 | A | G | 1 | a0001c0004t0001g0021 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.425-2211A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680907 | |||||||
| chr5:53680922 | T | G | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.425-2196T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680922 | |||||||
| chr5:53680995 | G | A | 257 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.425-2123G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53680995 | |||||||
| chr5:53681018 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.425-2100T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681018 | |||||||
| chr5:53681060 | G | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.425-2058G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681060 | |||||||
| chr5:53681066 | A | G | 21 | a0001c0001t0002g0002 a0001c0001t0002g0176 a0001c0001t0002g0177 others(18): Show |
22 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.425-2052A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681066 | |||||||
| chr5:53681125 | C | G | 171 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(168): Show |
173 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.425-1993C>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681125 | |||||||
| chr5:53681217 | G | A | 9 | a0001c0003t0002g0117 a0001c0003t0002g0120 a0001c0003t0002g0123 others(6): Show |
9 | HG00673.hp2 HG01433.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-1901G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681217 | |||||||
| chr5:53681323 | T | A | 17 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(14): Show |
17 | HG00140.hp1 HG01099.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.425-1795T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681323 | |||||||
| chr5:53681353 | C | T | 2 | a0001c0001t0002g0195 a0001c0001t0002g0197 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.425-1765C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681353 | |||||||
| chr5:53681391 | G | T | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.425-1727G>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681391 | |||||||
| chr5:53681605 | T | G | 1 | a0001c0001t0001g0315 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.425-1513T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681605 | |||||||
| chr5:53681642 | T | A | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.425-1476T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681642 | |||||||
| chr5:53681750 | T | A | 61 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0143 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.425-1368T>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53681750 | |||||||
| chr5:53681981 | CACTT | C | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.425-1135_425-1132d others(6): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53681981 | ||||||
| chr5:53682058 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.425-1060A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682058 | |||||||
| chr5:53682074 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.425-1044T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682074 | |||||||
| chr5:53682188 | T | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0348 |
2 | HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.425-930T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682188 | |||||||
| chr5:53682205 | G | A | 2 | a0001c0002t0001g0157 a0001c0002t0001g0161 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.425-913G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682205 | |||||||
| chr5:53682373 | C | T | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.425-745C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682373 | |||||||
| chr5:53682500 | C | T | 2 | a0001c0003t0001g0156 a0001c0003t0001g0158 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.425-618C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682500 | |||||||
| chr5:53682512 | A | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.425-606A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682512 | |||||||
| chr5:53682519 | C | CAGAT | 97 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.425-592_425-589dup others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53682519 | ||||||
| chr5:53682566 | T | TAATC | 51 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0096 others(48): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.425-550_425-547dup others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53682566 | ||||||
| chr5:53682595 | T | C | 1 | a0001c0003t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.425-523T>C | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682595 | |||||||
| chr5:53682600 | C | A | 1 | a0001c0003t0002g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.425-518C>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682600 | |||||||
| chr5:53682687 | G | A | 275 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(272): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.425-431G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682687 | |||||||
| chr5:53682884 | T | G | 2 | a0001c0004t0001g0034 a0001c0004t0001g0038 |
2 | NA18974.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.425-234T>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682884 | |||||||
| chr5:53682892 | C | T | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.425-226C>T | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682892 | |||||||
| chr5:53682943 | AG | A | 7 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0299 others(4): Show |
7 | HG01346.hp1 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.425-174delG | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682943 | |||||||
| chr5:53682944 | G | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0276 others(87): Show |
91 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.425-174G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682944 | |||||||
| chr5:53682946 | GGATT | G | 276 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0164 others(273): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.425-167_425-164del others(4): Show |
NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 53682946 | ||||||
| chr5:53682995 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.425-123A>G | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53682995 | |||||||
| chr5:53683048 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.425-70G>A | NDUFS4 | ENSG00000164258.12 | transcript | ENST00000296684.10 | protein_coding | 4/4 | chr5 | 53683048 |