Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 286097 |
|---|---|
| ensemblid | ENSG00000155970.12 |
| hgncid | 27820 |
| symbol | MICU3 |
| name | mitochondrial calcium uptake family member 3 |
| refseq_nuc | NM_181723.3 |
| refseq_prot | NP_859074.1 |
| ensembl_nuc | ENST00000318063.10 |
| ensembl_prot | ENSP00000321455.5 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 17027238 |
| end | 17122642 |
| strand | + |
| ver | v1.2 |
| region | chr8:17027238-17122642 |
| region5000 | chr8:17022238-17127642 |
| regionname0 | MICU3_chr8_17027238_17122642 |
| regionname5000 | MICU3_chr8_17022238_17127642 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 530 | 340 | 65 | 61 | 166 | 12 | 34 | 128 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0002 | 0/0 | 530 | 29 | 28 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0003 | 0/0 | 530 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0004 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0005 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0006 | 0/0 | 530 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1593 | 313 | 62 | 54 | 154 | 11 | 30 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0002 | 0/0 | 1593 | 25 | 24 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0003 | 0/0 | 1593 | 15 | 0 | 6 | 4 | 1 | 4 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0004 | 0/0 | 1593 | 6 | 0 | 0 | 6 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0005 | 0/0 | 1593 | 4 | 4 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0006 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0007 | 0/0 | 1593 | 2 | 0 | 2 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0008 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0009 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0010 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0011 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0012 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| c0013 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2398 | 111 | 42 | 24 | 34 | 2 | 9 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0002 | 1/0 | 2398 | 97 | 12 | 16 | 49 | 4 | 15 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0003 | 0/1 | 2398 | 61 | 6 | 16 | 30 | 5 | 3 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0004 | 0/0 | 2398 | 43 | 0 | 4 | 37 | 0 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0005 | 0/0 | 2398 | 8 | 7 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0006 | 0/0 | 2398 | 7 | 7 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0007 | 0/0 | 2398 | 4 | 0 | 0 | 4 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0008 | 0/0 | 2398 | 4 | 4 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0009 | 0/0 | 2398 | 4 | 0 | 0 | 4 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0010 | 0/0 | 2398 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0011 | 0/0 | 2398 | 3 | 0 | 1 | 0 | 0 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0012 | 0/0 | 2398 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0013 | 0/0 | 2398 | 3 | 1 | 1 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0014 | 0/0 | 2398 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0015 | 0/0 | 2398 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0016 | 0/0 | 2398 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0017 | 0/0 | 2398 | 2 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0018 | 0/0 | 2398 | 2 | 0 | 0 | 0 | 0 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0019 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0020 | 0/0 | 2398 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0021 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0022 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0023 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0024 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0025 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0026 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0027 | 0/0 | 2398 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0028 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0029 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| t0030 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1593 | 313 | 62 | 54 | 154 | 11 | 30 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0003 | 0/0 | 1593 | 15 | 0 | 6 | 4 | 1 | 4 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0004 | 0/0 | 1593 | 6 | 0 | 0 | 6 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0006 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0009 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0011 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0013 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0002c0002 | 0/0 | 1593 | 25 | 24 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0002c0005 | 0/0 | 1593 | 4 | 4 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0003c0007 | 0/0 | 1593 | 2 | 0 | 2 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0004c0010 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0005c0012 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0006c0008 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3990 | 83 | 18 | 22 | 32 | 2 | 9 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0002 | 1/0 | 3990 | 86 | 12 | 10 | 47 | 3 | 13 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0003 | 0/1 | 3990 | 59 | 5 | 16 | 29 | 5 | 3 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0004 | 0/0 | 3990 | 40 | 0 | 4 | 34 | 0 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0005 | 0/0 | 3990 | 6 | 6 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0006 | 0/0 | 3990 | 7 | 7 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0008 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0009 | 0/0 | 3990 | 4 | 0 | 0 | 4 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0010 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0011 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0012 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0013 | 0/0 | 3990 | 3 | 1 | 1 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0014 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0015 | 0/0 | 3990 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0016 | 0/0 | 3990 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0018 | 0/0 | 3990 | 2 | 0 | 0 | 0 | 0 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0019 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0023 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0024 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0025 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0027 | 0/0 | 3990 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0028 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0029 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0001t0030 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0003t0001 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0003t0002 | 0/0 | 3990 | 7 | 0 | 4 | 0 | 1 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0003t0007 | 0/0 | 3990 | 3 | 0 | 0 | 3 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0003t0011 | 0/0 | 3990 | 2 | 0 | 0 | 0 | 0 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0003t0020 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0003t0022 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0004t0001 | 0/0 | 3990 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0004t0002 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0004t0004 | 0/0 | 3990 | 3 | 0 | 0 | 3 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0006t0001 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0009t0001 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0011t0003 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0001c0013t0021 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0002c0002t0001 | 0/0 | 3990 | 17 | 17 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0002c0002t0003 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0002c0002t0005 | 0/0 | 3990 | 2 | 1 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0002c0002t0008 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0002c0002t0017 | 0/0 | 3990 | 2 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0002c0005t0001 | 0/0 | 3990 | 4 | 4 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0003c0007t0002 | 0/0 | 3990 | 2 | 0 | 2 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0004c0010t0002 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0005c0012t0007 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| a0006c0008t0026 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | copy fasta | chr8 | 17022238 | 17127642 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0009g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0009g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0009g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0010g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0011g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0012g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0013g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0013g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0014g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0014g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0015g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0015g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0016g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0016g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0018g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0018g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0019g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0023g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0024g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0025g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0027g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0028g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0029g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0001t0030g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0011g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0011g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0020g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0003t0022g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0004t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0004t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0004t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0004t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0006t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0006t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0006t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0009t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0011t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0013t0021g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0017g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0002t0017g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0005t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0005t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0005t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0002c0005t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0003c0007t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0003c0007t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0004c0010t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0005c0012t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0006c0008t0026g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0291 | EUR | GBR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0158 | EUR | GBR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0204 | EUR | GBR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0210 | EUR | FIN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0073 | EUR | FIN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00438 | hp1 | a0001 | c0004 | t0004 | g0207 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0200 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0203 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00735 | hp2 | a0001 | c0001 | t0013 | g0161 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01109 | hp2 | a0001 | c0009 | t0001 | g0019 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0322 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0039 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0325 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01255 | hp2 | a0001 | c0003 | t0002 | g0201 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0269 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01361 | hp2 | a0002 | c0002 | t0005 | g0190 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0292 | EUR | IBS | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0174 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01891 | hp2 | a0001 | c0006 | t0001 | g0239 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01928 | hp1 | a0001 | c0003 | t0020 | g0053 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01934 | hp2 | a0003 | c0007 | t0002 | g0106 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02004 | hp2 | a0003 | c0007 | t0002 | g0064 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02055 | hp2 | a0006 | c0008 | t0026 | g0184 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02071 | hp1 | a0001 | c0013 | t0021 | g0263 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02074 | hp1 | a0001 | c0004 | t0004 | g0206 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02083 | hp1 | a0001 | c0004 | t0001 | g0209 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0242 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02155 | hp1 | a0001 | c0003 | t0007 | g0038 | EAS | CDX | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02155 | hp2 | a0001 | c0001 | t0028 | g0302 | EAS | CDX | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02258 | hp2 | a0001 | c0006 | t0001 | g0237 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0023 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0006 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0227 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0031 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02630 | hp2 | a0002 | c0005 | t0001 | g0180 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02698 | hp1 | a0001 | c0003 | t0011 | g0061 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02698 | hp2 | a0001 | c0001 | t0018 | g0362 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0187 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0328 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0022 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0284 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02897 | hp2 | a0002 | c0005 | t0001 | g0181 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02922 | hp1 | a0002 | c0002 | t0017 | g0188 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02965 | hp2 | a0002 | c0002 | t0008 | g0172 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02970 | hp1 | a0001 | c0001 | t0030 | g0032 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0006 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0234 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0364 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0191 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03195 | hp2 | a0001 | c0006 | t0001 | g0238 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03209 | hp2 | a0001 | c0001 | t0012 | g0029 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03225 | hp1 | a0002 | c0005 | t0001 | g0175 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0235 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03486 | hp2 | a0002 | c0002 | t0017 | g0194 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03490 | hp1 | a0001 | c0003 | t0002 | g0202 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03491 | hp1 | a0001 | c0003 | t0011 | g0052 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0217 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | ESN | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03540 | hp1 | a0002 | c0005 | t0001 | g0171 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0357 | AFR | GWD | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0361 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03669 | hp1 | a0001 | c0001 | t0013 | g0224 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | STU | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0360 | SAS | PJL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | BEB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0265 | SAS | BEB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0341 | SAS | STU | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0068 | SAS | BEB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG04199 | hp1 | a0001 | c0003 | t0002 | g0054 | SAS | STU | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0363 | SAS | STU | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | STU | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | STU | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | STU | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | YRI | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | CHB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | YRI | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18906 | hp2 | a0002 | c0002 | t0005 | g0186 | AFR | YRI | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0307 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18949 | hp1 | a0001 | c0004 | t0001 | g0350 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18949 | hp2 | a0001 | c0004 | t0002 | g0208 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18952 | hp2 | a0001 | c0001 | t0019 | g0243 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18960 | hp2 | a0001 | c0004 | t0004 | g0012 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18970 | hp2 | a0001 | c0001 | t0015 | g0335 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18973 | hp2 | a0001 | c0001 | t0015 | g0319 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18974 | hp2 | a0001 | c0001 | t0016 | g0338 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18975 | hp2 | a0001 | c0011 | t0003 | g0199 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18977 | hp1 | a0001 | c0001 | t0024 | g0309 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18979 | hp2 | a0001 | c0001 | t0016 | g0088 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18985 | hp2 | a0001 | c0003 | t0007 | g0047 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18986 | hp1 | a0001 | c0001 | t0009 | g0336 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18998 | hp2 | a0005 | c0012 | t0007 | g0078 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18999 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18999 | hp2 | a0001 | c0001 | t0023 | g0249 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19000 | hp1 | a0004 | c0010 | t0002 | g0280 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0343 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19030 | hp1 | a0001 | c0001 | t0029 | g0123 | AFR | LWK | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | LWK | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0030 | AFR | LWK | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19070 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19074 | hp2 | a0001 | c0003 | t0022 | g0055 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19080 | hp2 | a0001 | c0003 | t0007 | g0036 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19084 | hp2 | a0001 | c0001 | t0009 | g0267 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | YRI | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA19240 | hp2 | a0002 | c0002 | t0008 | g0176 | AFR | YRI | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | ASW | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0166 | EUR | TSI | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA20752 | hp2 | a0001 | c0001 | t0027 | g0169 | EUR | TSI | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0290 | EUR | TSI | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | TSI | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA20905 | hp1 | a0001 | c0001 | t0018 | g0233 | SAS | GIH | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0089 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02486 | hp2 | a0002 | c0002 | t0008 | g0177 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | ACB | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03471 | hp1 | a0001 | c0001 | t0025 | g0018 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | MSL | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | USA | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0218 | AFR | USA | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0192 | AFR | USA | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0138 | REF | REF | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0133 | REF | REF | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:17027553
|
G | C | 2 | a0002a0006 | 30 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
missense_variant | MODERATE | c.274G>C | p.Gly92Arg | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/15 | 316/3990 | 274/1593 | 92/530 | chr8 | 17027553 | ||
| chr8:17027610
|
C | T | 1 | a0003 | 2 | HG01934.hp2 HG02004.hp2 |
missense_variant | MODERATE | c.331C>T | p.Pro111Ser | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/15 | 373/3990 | 331/1593 | 111/530 | chr8 | 17027610 | ||
| chr8:17064096
|
A | G | 1 | a0006 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.394A>G | p.Arg132Gly | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/15 | 436/3990 | 394/1593 | 132/530 | chr8 | 17064096 | ||
| chr8:17077829
|
C | T | 1 | a0004 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.614C>T | p.Ser205Leu | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/15 | 656/3990 | 614/1593 | 205/530 | chr8 | 17077829 | ||
| chr8:17087030
|
A | G | 1 | a0005 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.844A>G | p.Met282Val | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/15 | 886/3990 | 844/1593 | 282/530 | chr8 | 17087030 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:17027369
|
G | T | 1 | a0001c0013 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.90G>T | p.Arg30Arg | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/15 | 132/3990 | 90/1593 | 30/530 | chr8 | 17027369 | ||
| chr8:17027387
|
G | A | 1 | a0001c0006 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.108G>A | p.Leu36Leu | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/15 | 150/3990 | 108/1593 | 36/530 | chr8 | 17027387 | ||
| chr8:17027522
|
A | G | 1 | a0001c0006 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.243A>G | p.Val81Val | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/15 | 285/3990 | 243/1593 | 81/530 | chr8 | 17027522 | ||
| chr8:17027567
|
C | G | 2 | a0001c0003a0005c0012 | 16 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(13): Show |
synonymous_variant | LOW | c.288C>G | p.Thr96Thr | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/15 | 330/3990 | 288/1593 | 96/530 | chr8 | 17027567 | ||
| chr8:17077800
|
C | T | 1 | a0001c0011 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.585C>T | p.Leu195Leu | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/15 | 627/3990 | 585/1593 | 195/530 | chr8 | 17077800 | ||
| chr8:17085288
|
T | C | 1 | a0001c0004 | 6 | HG00438.hp1 HG02074.hp1 HG02083.hp1 others(3): Show |
synonymous_variant | LOW | c.747T>C | p.Asn249Asn | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/15 | 789/3990 | 747/1593 | 249/530 | chr8 | 17085288 | ||
| chr8:17114101
|
A | C | 2 | a0001c0009a0002c0005 | 5 | HG01109.hp2 HG02630.hp2 HG02897.hp2 others(2): Show |
synonymous_variant | LOW | c.1266A>C | p.Thr422Thr | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/15 | 1308/3990 | 1266/1593 | 422/530 | chr8 | 17114101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:17027249
|
C | T | 1 | a0001c0001t0030 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/15 | 31 | chr8 | 17027249 | |||||
| chr8:17120310
|
A | G | 1 | a0001c0001t0029 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*23A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 1535 | chr8 | 17120310 | |||||
| chr8:17120418
|
T | C | 1 | a0001c0001t0015 | 2 | NA18970.hp2 NA18973.hp2 |
3_prime_UTR_variant | MODIFIER | c.*131T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 1643 | chr8 | 17120418 | |||||
| chr8:17120491
|
A | G | 19 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(16): Show | 140 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*204A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 1716 | chr8 | 17120491 | |||||
| chr8:17120686
|
C | A | 1 | a0001c0001t0010 | 3 | HG02280.hp2 HG02615.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*399C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 1911 | chr8 | 17120686 | |||||
| chr8:17120697
|
C | G | 2 | a0001c0001t0029a0001c0001t0030 | 2 | HG02970.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*410C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 1922 | chr8 | 17120697 | |||||
| chr8:17120716
|
A | G | 1 | a0001c0001t0024 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*429A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 1941 | chr8 | 17120716 | |||||
| chr8:17120847
|
A | T | 1 | a0001c0001t0028 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*560A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 2072 | chr8 | 17120847 | |||||
| chr8:17120891
|
A | G | 3 | a0001c0001t0003a0001c0011t0003a0002c0002t0003 | 61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*604A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 2116 | chr8 | 17120891 | |||||
| chr8:17120893
|
A | G | 1 | a0001c0001t0018 | 2 | HG02698.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*606A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 2118 | chr8 | 17120893 | |||||
| chr8:17121072
|
A | G | 1 | a0001c0001t0023 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*785A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 2297 | chr8 | 17121072 | |||||
| chr8:17121155
|
A | T | 3 | a0001c0001t0008a0001c0001t0014a0002c0002t0008 | 7 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*868A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 2380 | chr8 | 17121155 | |||||
| chr8:17121177
|
G | C | 3 | a0001c0001t0006a0001c0001t0010a0001c0001t0025 | 11 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*890G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 2402 | chr8 | 17121177 | |||||
| chr8:17121268
|
T | A | 1 | a0001c0001t0009 | 4 | NA18986.hp1 NA18999.hp1 NA19070.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*981T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 2493 | chr8 | 17121268 | |||||
| chr8:17121599
|
C | A | 1 | a0001c0001t0019 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1312C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 2824 | chr8 | 17121599 | |||||
| chr8:17121607
|
A | C | 4 | a0001c0001t0011a0001c0003t0007a0001c0003t0011others(1): Show | 7 | HG01175.hp1 HG02155.hp1 HG02698.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1320A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 2832 | chr8 | 17121607 | |||||
| chr8:17121633
|
A | T | 1 | a0001c0003t0022 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 2858 | chr8 | 17121633 | |||||
| chr8:17121984
|
G | T | 2 | a0001c0001t0005a0002c0002t0005 | 8 | HG01361.hp2 HG02145.hp1 HG02976.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1697G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3209 | chr8 | 17121984 | |||||
| chr8:17122102
|
C | T | 17 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(14): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1815C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3327 | chr8 | 17122102 | |||||
| chr8:17122115
|
G | C | 19 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(16): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1828G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3340 | chr8 | 17122115 | |||||
| chr8:17122127
|
T | C | 1 | a0001c0001t0018 | 2 | HG02698.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1840T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3352 | chr8 | 17122127 | |||||
| chr8:17122129
|
C | G | 1 | a0001c0001t0016 | 2 | NA18974.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1842C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3354 | chr8 | 17122129 | |||||
| chr8:17122180
|
T | C | 1 | a0006c0008t0026 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1893T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3405 | chr8 | 17122180 | |||||
| chr8:17122257
|
G | A | 1 | a0002c0002t0017 | 2 | HG02922.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1970G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3482 | chr8 | 17122257 | |||||
| chr8:17122440
|
A | T | 1 | a0001c0001t0009 | 4 | NA18986.hp1 NA18999.hp1 NA19070.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2153A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3665 | chr8 | 17122440 | |||||
| chr8:17122518
|
T | C | 1 | a0001c0013t0021 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2231T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3743 | chr8 | 17122518 | |||||
| chr8:17122520
|
T | A | 10 | a0001c0001t0004a0001c0001t0011a0001c0001t0019others(7): Show | 52 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2233T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3745 | chr8 | 17122520 | |||||
| chr8:17122572
|
A | C | 1 | a0001c0001t0012 | 3 | HG02630.hp1 HG03209.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2285A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3797 | chr8 | 17122572 | |||||
| chr8:17122588
|
G | T | 1 | a0001c0001t0027 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2301G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 15/15 | 3813 | chr8 | 17122588 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:17027779
|
C | T | 1 | a0002c0002t0001g0364 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.381+119C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17027779 | ||||||
| chr8:17027833
|
T | C | 1 | a0001c0001t0008g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.381+173T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17027833 | ||||||
| chr8:17027845
|
G | C | 1 | a0001c0004t0004g0012 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.381+185G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17027845 | ||||||
| chr8:17027931
|
C | T | 1 | a0001c0001t0002g0363 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381+271C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17027931 | ||||||
| chr8:17027972
|
A | G | 1 | a0001c0001t0018g0362 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.381+312A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17027972 | ||||||
| chr8:17028033
|
A | G | 3 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361 | 3 | HG00642.hp1 HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.381+373A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028033 | ||||||
| chr8:17028055
|
A | G | 1 | a0001c0001t0008g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.381+395A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028055 | ||||||
| chr8:17028078
|
G | C | 1 | a0001c0001t0002g0013 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.381+418G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028078 | ||||||
| chr8:17028126
|
T | C | 18 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0005g0027others(15): Show | 18 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.381+466T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028126 | ||||||
| chr8:17028283
|
G | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+623G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028283 | ||||||
| chr8:17028344
|
A | T | 175 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(172): Show | 181 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.381+684A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028344 | ||||||
| chr8:17028493
|
A | G | 1 | a0001c0001t0002g0358 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.381+833A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028493 | ||||||
| chr8:17028499
|
A | G | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0003g0357others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.381+839A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028499 | ||||||
| chr8:17028539
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.381+879G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028539 | ||||||
| chr8:17028677
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(24): Show | 30 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.381+1017G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028677 | ||||||
| chr8:17028687
|
C | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(24): Show | 30 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.381+1027C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028687 | ||||||
| chr8:17028736
|
C | G | 1 | a0001c0001t0003g0210 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.381+1076C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028736 | ||||||
| chr8:17028752
|
A | T | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(99): Show | 103 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.381+1092A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028752 | ||||||
| chr8:17028822
|
G | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+1162G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028822 | ||||||
| chr8:17028876
|
A | G | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.381+1216A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17028876 | ||||||
| chr8:17028920
|
A | AT | 45 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0252others(42): Show | 47 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.381+1264dupT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17028920 | |||||
| chr8:17029068
|
A | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0205 | 3 | HG02809.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.381+1408A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17029068 | ||||||
| chr8:17029305
|
G | T | 5 | a0001c0003t0002g0200a0001c0003t0002g0201a0001c0003t0002g0202others(2): Show | 5 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+1645G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17029305 | ||||||
| chr8:17029424
|
C | T | 41 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(38): Show | 43 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.381+1764C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17029424 | ||||||
| chr8:17029530
|
A | T | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.381+1870A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17029530 | ||||||
| chr8:17029639
|
C | A | 4 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0003g0005others(1): Show | 5 | HG01081.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+1979C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17029639 | ||||||
| chr8:17029889
|
A | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(23): Show | 29 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.381+2229A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17029889 | ||||||
| chr8:17029905
|
C | G | 1 | a0001c0011t0003g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.381+2245C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17029905 | ||||||
| chr8:17029976
|
C | G | 213 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(210): Show | 220 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.381+2316C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17029976 | ||||||
| chr8:17030007
|
C | A | 1 | a0002c0005t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.381+2347C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030007 | ||||||
| chr8:17030076
|
T | G | 1 | a0001c0001t0002g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.381+2416T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030076 | ||||||
| chr8:17030095
|
A | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+2435A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030095 | ||||||
| chr8:17030097
|
T | A | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.381+2437T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030097 | ||||||
| chr8:17030233
|
T | A | 126 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(123): Show | 129 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.381+2573T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030233 | ||||||
| chr8:17030459
|
T | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+2799T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030459 | ||||||
| chr8:17030587
|
T | C | 4 | a0001c0001t0001g0286a0001c0001t0003g0283a0001c0001t0003g0284others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+2927T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030587 | ||||||
| chr8:17030603
|
G | A | 1 | a0001c0001t0004g0242 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.381+2943G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030603 | ||||||
| chr8:17030810
|
A | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(23): Show | 29 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.381+3150A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030810 | ||||||
| chr8:17030821
|
C | G | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(1): Show | 4 | HG00642.hp2 HG01123.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+3161C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030821 | ||||||
| chr8:17030830
|
A | G | 43 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(40): Show | 45 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.381+3170A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030830 | ||||||
| chr8:17030832
|
T | C | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | NA18973.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.381+3172T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030832 | ||||||
| chr8:17030834
|
G | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | NA18973.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.381+3174G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030834 | ||||||
| chr8:17030835
|
G | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | NA18973.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.381+3175G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030835 | ||||||
| chr8:17030837
|
C | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | NA18973.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.381+3177C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030837 | ||||||
| chr8:17030838
|
T | C | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 2 | NA18973.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.381+3178T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030838 | ||||||
| chr8:17030893
|
C | T | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.381+3233C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17030893 | ||||||
| chr8:17031124
|
A | G | 1 | a0001c0004t0001g0209 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.381+3464A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031124 | ||||||
| chr8:17031171
|
T | C | 127 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(124): Show | 131 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.381+3511T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031171 | ||||||
| chr8:17031262
|
T | TTTA | 130 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0074others(127): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.381+3641_381+3643d others(5): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
T | TTTATTA | 87 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0058others(84): Show | 92 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.381+3638_381+3643d others(8): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
T | TTTATTAT others(2): Show |
41 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0041others(38): Show | 42 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.381+3635_381+3643d others(11): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
T | TTTATTAT others(5): Show |
1 | a0001c0003t0007g0036 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.381+3632_381+3643d others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
T | TTTTTTAT others(2): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0205a0002c0002t0008g0177 | 4 | HG02486.hp2 HG02809.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+3604_381+3605i others(11): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
T | TTTTTTAT others(5): Show |
1 | a0002c0002t0008g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.381+3604_381+3605i others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
T | TTTTTTTT others(2): Show |
13 | a0002c0002t0001g0003a0002c0002t0001g0182a0002c0002t0001g0183others(10): Show | 14 | HG01361.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.381+3604_381+3605i others(11): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
T | TTTTTTTT others(5): Show |
1 | a0002c0005t0001g0180 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.381+3604_381+3605i others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
T | TTTTTTTT others(11): Show |
4 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+3604_381+3605i others(20): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
TTTA | T | 15 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0001g0353others(12): Show | 15 | HG01884.hp2 HG02257.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.381+3641_381+3643d others(5): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
TTTATTA | T | 4 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0008g0011others(1): Show | 4 | HG00438.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+3638_381+3643d others(8): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
TTTATTAT others(2): Show |
T | 3 | a0001c0001t0001g0164a0001c0001t0003g0165a0001c0001t0003g0357 | 3 | HG02129.hp1 HG03540.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.381+3635_381+3643d others(11): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031262
|
TTTATTAT others(8): Show |
T | 1 | a0001c0001t0003g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.381+3629_381+3643d others(17): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17031262 | |||||
| chr8:17031268
|
A | T | 9 | a0002c0002t0001g0178a0002c0002t0001g0191a0002c0002t0001g0192others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+3608A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031268 | ||||||
| chr8:17031271
|
A | T | 8 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0193others(5): Show | 8 | HG02257.hp2 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+3611A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031271 | ||||||
| chr8:17031326
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.381+3666C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031326 | ||||||
| chr8:17031329
|
T | C | 178 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(175): Show | 185 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.381+3669T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031329 | ||||||
| chr8:17031349
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.381+3689G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031349 | ||||||
| chr8:17031441
|
A | G | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.381+3781A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031441 | ||||||
| chr8:17031498
|
A | C | 1 | a0001c0001t0001g0049 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.381+3838A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031498 | ||||||
| chr8:17031627
|
C | T | 1 | a0001c0001t0003g0124 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.381+3967C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031627 | ||||||
| chr8:17031704
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.381+4044A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031704 | ||||||
| chr8:17031740
|
G | C | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0005g0027others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.381+4080G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031740 | ||||||
| chr8:17031796
|
A | G | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+4136A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031796 | ||||||
| chr8:17031827
|
G | T | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381+4167G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031827 | ||||||
| chr8:17031831
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.381+4171T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031831 | ||||||
| chr8:17031871
|
T | G | 177 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(174): Show | 184 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+4211T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031871 | ||||||
| chr8:17031925
|
A | T | 175 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(172): Show | 181 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.381+4265A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17031925 | ||||||
| chr8:17032125
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA18991.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.381+4465G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032125 | ||||||
| chr8:17032140
|
A | T | 1 | a0001c0001t0001g0298 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.381+4480A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032140 | ||||||
| chr8:17032153
|
C | T | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.381+4493C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032153 | ||||||
| chr8:17032182
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA18991.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.381+4522T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032182 | ||||||
| chr8:17032291
|
A | G | 1 | a0001c0001t0002g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.381+4631A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032291 | ||||||
| chr8:17032313
|
A | G | 1 | a0001c0001t0002g0363 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381+4653A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032313 | ||||||
| chr8:17032343
|
G | A | 4 | a0001c0001t0006g0014a0001c0001t0006g0017a0001c0001t0025g0018others(1): Show | 4 | HG01109.hp2 HG02886.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+4683G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032343 | ||||||
| chr8:17032359
|
T | G | 43 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(40): Show | 45 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.381+4699T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032359 | ||||||
| chr8:17032431
|
T | G | 43 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(40): Show | 45 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.381+4771T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032431 | ||||||
| chr8:17032501
|
T | C | 2 | a0001c0001t0002g0050a0001c0001t0002g0073 | 2 | HG00280.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.381+4841T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032501 | ||||||
| chr8:17032512
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.381+4852T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032512 | ||||||
| chr8:17032520
|
G | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+4860G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032520 | ||||||
| chr8:17032707
|
C | T | 25 | a0002c0002t0001g0003a0002c0002t0001g0179a0002c0002t0001g0182others(22): Show | 26 | HG01361.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.381+5047C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032707 | ||||||
| chr8:17032715
|
C | T | 202 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(199): Show | 209 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(206): Show |
intron_variant | MODIFIER | c.381+5055C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032715 | ||||||
| chr8:17032757
|
C | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+5097C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032757 | ||||||
| chr8:17032790
|
C | G | 1 | a0001c0001t0003g0072 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.381+5130C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032790 | ||||||
| chr8:17032823
|
C | T | 1 | a0001c0001t0002g0327 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.381+5163C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032823 | ||||||
| chr8:17032876
|
C | G | 1 | a0001c0001t0001g0326 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.381+5216C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032876 | ||||||
| chr8:17032921
|
A | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0205 | 3 | HG02809.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.381+5261A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032921 | ||||||
| chr8:17032978
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.381+5318C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17032978 | ||||||
| chr8:17033035
|
C | G | 43 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(40): Show | 45 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.381+5375C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033035 | ||||||
| chr8:17033252
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.381+5592G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033252 | ||||||
| chr8:17033407
|
G | C | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381+5747G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033407 | ||||||
| chr8:17033416
|
C | G | 43 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(40): Show | 45 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.381+5756C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033416 | ||||||
| chr8:17033434
|
T | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0051 | 3 | NA18957.hp2 NA18983.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.381+5774T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033434 | ||||||
| chr8:17033459
|
C | T | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.381+5799C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033459 | ||||||
| chr8:17033604
|
T | A | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+5944T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033604 | ||||||
| chr8:17033631
|
A | G | 175 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(172): Show | 181 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.381+5971A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033631 | ||||||
| chr8:17033631
|
A | T | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381+5971A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033631 | ||||||
| chr8:17033776
|
G | A | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.381+6116G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033776 | ||||||
| chr8:17033782
|
G | T | 1 | a0001c0001t0003g0325 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.381+6122G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033782 | ||||||
| chr8:17033917
|
G | A | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.381+6257G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033917 | ||||||
| chr8:17033980
|
A | T | 43 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(40): Show | 45 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.381+6320A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033980 | ||||||
| chr8:17033995
|
C | T | 1 | a0001c0001t0019g0243 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.381+6335C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17033995 | ||||||
| chr8:17034021
|
A | G | 43 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(40): Show | 45 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.381+6361A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034021 | ||||||
| chr8:17034076
|
C | G | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG00621.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.381+6416C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034076 | ||||||
| chr8:17034135
|
A | G | 1 | a0001c0009t0001g0019 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.381+6475A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034135 | ||||||
| chr8:17034162
|
A | G | 1 | a0001c0001t0004g0276 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.381+6502A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034162 | ||||||
| chr8:17034205
|
C | T | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.381+6545C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034205 | ||||||
| chr8:17034252
|
A | G | 80 | a0001c0001t0001g0286a0001c0001t0001g0293a0001c0001t0001g0294others(77): Show | 80 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.381+6592A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034252 | ||||||
| chr8:17034324
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.381+6664C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034324 | ||||||
| chr8:17034340
|
A | T | 1 | a0001c0001t0002g0275 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.381+6680A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034340 | ||||||
| chr8:17034383
|
A | G | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381+6723A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034383 | ||||||
| chr8:17034445
|
A | T | 126 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(123): Show | 129 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.381+6785A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034445 | ||||||
| chr8:17034465
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.381+6805G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034465 | ||||||
| chr8:17034596
|
A | C | 1 | a0001c0009t0001g0019 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.381+6936A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034596 | ||||||
| chr8:17034627
|
T | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(22): Show | 28 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.381+6967T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034627 | ||||||
| chr8:17034836
|
T | C | 2 | a0001c0001t0004g0242a0001c0001t0004g0251 | 2 | HG02148.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.381+7176T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17034836 | ||||||
| chr8:17035027
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0070 | 2 | HG01081.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.381+7367C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035027 | ||||||
| chr8:17035078
|
G | A | 43 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(40): Show | 45 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.381+7418G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035078 | ||||||
| chr8:17035123
|
G | A | 1 | a0001c0001t0003g0230 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.381+7463G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035123 | ||||||
| chr8:17035214
|
A | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(23): Show | 29 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.381+7554A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035214 | ||||||
| chr8:17035267
|
G | C | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.381+7607G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035267 | ||||||
| chr8:17035290
|
G | C | 1 | a0001c0001t0003g0076 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.381+7630G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035290 | ||||||
| chr8:17035320
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.381+7660T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035320 | ||||||
| chr8:17035500
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA18991.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.381+7840G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035500 | ||||||
| chr8:17035699
|
T | C | 1 | a0001c0001t0003g0077 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.381+8039T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035699 | ||||||
| chr8:17035882
|
G | A | 93 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(90): Show | 93 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.381+8222G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035882 | ||||||
| chr8:17035934
|
A | G | 1 | a0001c0003t0007g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.381+8274A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035934 | ||||||
| chr8:17035959
|
A | T | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.381+8299A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035959 | ||||||
| chr8:17035999
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.381+8339C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17035999 | ||||||
| chr8:17036000
|
G | A | 96 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(93): Show | 96 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.381+8340G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036000 | ||||||
| chr8:17036045
|
C | T | 3 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0001t0012g0031 | 3 | HG02630.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.381+8385C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036045 | ||||||
| chr8:17036054
|
G | A | 1 | a0001c0003t0011g0052 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.381+8394G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036054 | ||||||
| chr8:17036121
|
C | T | 1 | a0002c0002t0001g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.381+8461C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036121 | ||||||
| chr8:17036124
|
A | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0205 | 3 | HG02809.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.381+8464A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036124 | ||||||
| chr8:17036147
|
G | A | 8 | a0002c0002t0001g0182a0002c0002t0001g0183a0002c0002t0001g0185others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+8487G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036147 | ||||||
| chr8:17036155
|
G | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+8495G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036155 | ||||||
| chr8:17036162
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.381+8502C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036162 | ||||||
| chr8:17036178
|
G | A | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.381+8518G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036178 | ||||||
| chr8:17036300
|
C | A | 12 | a0001c0003t0002g0039a0001c0003t0002g0054a0001c0003t0002g0200others(9): Show | 12 | HG00639.hp2 HG00735.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.381+8640C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036300 | ||||||
| chr8:17036339
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.381+8679A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036339 | ||||||
| chr8:17036382
|
T | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(27): Show | 33 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.381+8722T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036382 | ||||||
| chr8:17036499
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.381+8839G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036499 | ||||||
| chr8:17036538
|
A | C | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.381+8878A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036538 | ||||||
| chr8:17036539
|
A | G | 100 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(97): Show | 100 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.381+8879A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036539 | ||||||
| chr8:17036591
|
G | C | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.381+8931G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036591 | ||||||
| chr8:17036628
|
T | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(26): Show | 32 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.381+8968T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036628 | ||||||
| chr8:17036638
|
G | T | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+8978G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036638 | ||||||
| chr8:17036766
|
C | T | 69 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0297others(66): Show | 69 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.381+9106C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036766 | ||||||
| chr8:17036804
|
C | T | 1 | a0001c0001t0006g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.381+9144C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036804 | ||||||
| chr8:17036816
|
G | A | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.381+9156G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036816 | ||||||
| chr8:17036856
|
G | A | 1 | a0001c0001t0006g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.381+9196G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036856 | ||||||
| chr8:17036894
|
C | T | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.381+9234C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036894 | ||||||
| chr8:17036895
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.381+9235G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036895 | ||||||
| chr8:17036909
|
G | A | 1 | a0001c0001t0012g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.381+9249G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036909 | ||||||
| chr8:17036932
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.381+9272T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036932 | ||||||
| chr8:17036935
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.381+9275C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036935 | ||||||
| chr8:17036948
|
C | T | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.381+9288C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036948 | ||||||
| chr8:17036962
|
G | A | 4 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+9302G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036962 | ||||||
| chr8:17036963
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0018g0362 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.381+9303C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036963 | ||||||
| chr8:17036964
|
G | A | 1 | a0001c0004t0001g0350 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.381+9304G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036964 | ||||||
| chr8:17036982
|
C | G | 29 | a0002c0002t0001g0003a0002c0002t0001g0178a0002c0002t0001g0179others(26): Show | 30 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.381+9322C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036982 | ||||||
| chr8:17036982
|
C | T | 2 | a0001c0001t0005g0218a0001c0001t0010g0227 | 2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.381+9322C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036982 | ||||||
| chr8:17036983
|
G | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+9323G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036983 | ||||||
| chr8:17036993
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.381+9333C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036993 | ||||||
| chr8:17036997
|
C | T | 1 | a0001c0001t0003g0295 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.381+9337C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17036997 | ||||||
| chr8:17037006
|
C | G | 163 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(160): Show | 168 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.381+9346C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037006 | ||||||
| chr8:17037044
|
G | A | 1 | a0001c0001t0005g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.381+9384G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037044 | ||||||
| chr8:17037057
|
C | T | 3 | a0001c0003t0007g0036a0001c0003t0007g0047a0005c0012t0007g0078 | 3 | NA18985.hp2 NA18998.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.381+9397C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037057 | ||||||
| chr8:17037078
|
C | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0073 | 2 | HG00280.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.381+9418C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037078 | ||||||
| chr8:17037099
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.381+9439C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037099 | ||||||
| chr8:17037102
|
C | G | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.381+9442C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037102 | ||||||
| chr8:17037108
|
C | T | 3 | a0001c0001t0001g0321a0001c0001t0002g0345a0001c0001t0011g0322 | 3 | HG00741.hp2 HG01167.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.381+9448C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037108 | ||||||
| chr8:17037115
|
G | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0205others(39): Show | 44 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.381+9455G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037115 | ||||||
| chr8:17037125
|
A | C | 2 | a0001c0001t0002g0050a0001c0001t0002g0073 | 2 | HG00280.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.381+9465A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037125 | ||||||
| chr8:17037159
|
C | T | 1 | a0001c0001t0004g0274 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.381+9499C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037159 | ||||||
| chr8:17037163
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0205 | 3 | HG02809.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.381+9503C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037163 | ||||||
| chr8:17037170
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.381+9510C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037170 | ||||||
| chr8:17037187
|
CT | C | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+9528delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037187 | ||||||
| chr8:17037191
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.381+9531C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037191 | ||||||
| chr8:17037262
|
C | T | 29 | a0002c0002t0001g0003a0002c0002t0001g0178a0002c0002t0001g0179others(26): Show | 30 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.381+9602C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037262 | ||||||
| chr8:17037275
|
G | A | 2 | a0001c0001t0002g0127a0001c0001t0002g0129 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.381+9615G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037275 | ||||||
| chr8:17037278
|
G | A | 25 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(22): Show | 28 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.381+9618G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037278 | ||||||
| chr8:17037296
|
A | C | 16 | a0002c0002t0001g0003a0002c0002t0001g0179a0002c0002t0001g0182others(13): Show | 17 | HG01361.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.381+9636A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037296 | ||||||
| chr8:17037333
|
C | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+9673C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037333 | ||||||
| chr8:17037367
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(22): Show | 28 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.381+9707C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037367 | ||||||
| chr8:17037383
|
C | T | 25 | a0002c0002t0001g0003a0002c0002t0001g0179a0002c0002t0001g0182others(22): Show | 26 | HG01361.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.381+9723C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037383 | ||||||
| chr8:17037543
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | NA18967.hp1 NA18985.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.381+9883C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037543 | ||||||
| chr8:17037566
|
T | G | 3 | a0001c0001t0001g0286a0001c0001t0003g0284a0001c0001t0003g0285 | 3 | HG02717.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.381+9906T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037566 | ||||||
| chr8:17037600
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.381+9940A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037600 | ||||||
| chr8:17037607
|
G | A | 94 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(91): Show | 94 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.381+9947G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037607 | ||||||
| chr8:17037647
|
G | A | 1 | a0001c0001t0006g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.381+9987G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037647 | ||||||
| chr8:17037719
|
C | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+10059C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037719 | ||||||
| chr8:17037738
|
C | T | 1 | a0001c0001t0002g0320 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.381+10078C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17037738 | ||||||
| chr8:17038287
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0205 | 3 | HG02809.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.381+10627G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038287 | ||||||
| chr8:17038320
|
A | T | 1 | a0001c0001t0003g0069 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.381+10660A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038320 | ||||||
| chr8:17038398
|
G | A | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.381+10738G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038398 | ||||||
| chr8:17038600
|
A | T | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.381+10940A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038600 | ||||||
| chr8:17038830
|
G | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0070a0001c0001t0002g0001 | 4 | HG00639.hp1 HG01081.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+11170G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038830 | ||||||
| chr8:17038843
|
C | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+11183C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038843 | ||||||
| chr8:17038952
|
CA | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0205others(64): Show | 72 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.381+11307delA | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17038952 | |||||
| chr8:17038952
|
CAA | C | 136 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(133): Show | 138 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.381+11306_381+1130 others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17038952 | |||||
| chr8:17038960
|
A | T | 136 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(133): Show | 138 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.381+11300A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038960 | ||||||
| chr8:17038964
|
A | T | 169 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(166): Show | 175 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.381+11304A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038964 | ||||||
| chr8:17038965
|
A | T | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+11305A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038965 | ||||||
| chr8:17038967
|
AT | A | 5 | a0001c0001t0001g0173a0001c0001t0006g0020a0001c0006t0001g0237others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+11308delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038967 | ||||||
| chr8:17038968
|
T | A | 3 | a0001c0001t0001g0079a0001c0001t0003g0081a0001c0001t0004g0080 | 3 | HG01167.hp2 NA18955.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.381+11308T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17038968 | ||||||
| chr8:17039110
|
G | T | 2 | a0001c0001t0002g0360a0001c0001t0002g0361 | 2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.381+11450G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17039110 | ||||||
| chr8:17039128
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.381+11468T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17039128 | ||||||
| chr8:17039227
|
A | G | 1 | a0001c0001t0004g0273 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.381+11567A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17039227 | ||||||
| chr8:17039236
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.381+11576G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17039236 | ||||||
| chr8:17039271
|
A | G | 1 | a0001c0001t0002g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.381+11611A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17039271 | ||||||
| chr8:17039732
|
A | G | 7 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+12072A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17039732 | ||||||
| chr8:17039754
|
GA | G | 4 | a0002c0002t0001g0178a0002c0002t0008g0172a0002c0002t0008g0176others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+12097delA | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17039754 | |||||
| chr8:17039895
|
C | CT | 141 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0041others(138): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.381+12264dupT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17039895 | |||||
| chr8:17039895
|
C | CTT | 37 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(34): Show | 38 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.381+12263_381+1226 others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17039895 | |||||
| chr8:17039895
|
CT | C | 59 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(56): Show | 61 | HG00408.hp1 HG00597.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.381+12264delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17039895 | |||||
| chr8:17039895
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.381+12254_381+1226 others(15): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17039895 | |||||
| chr8:17039895
|
CTTTTTTT others(8): Show |
C | 1 | a0004c0010t0002g0280 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.381+12250_381+1226 others(19): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17039895 | |||||
| chr8:17040033
|
G | A | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+12373G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17040033 | ||||||
| chr8:17040034
|
A | T | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+12374A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17040034 | ||||||
| chr8:17040057
|
G | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0216a0001c0001t0001g0219others(9): Show | 14 | HG00738.hp1 HG02451.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.381+12397G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17040057 | ||||||
| chr8:17040149
|
C | T | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.381+12489C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17040149 | ||||||
| chr8:17040159
|
C | T | 1 | a0001c0009t0001g0019 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.381+12499C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17040159 | ||||||
| chr8:17040403
|
C | G | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.381+12743C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17040403 | ||||||
| chr8:17040556
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(22): Show | 28 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.381+12896C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17040556 | ||||||
| chr8:17040602
|
G | T | 1 | a0001c0001t0004g0247 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.381+12942G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17040602 | ||||||
| chr8:17040623
|
T | C | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+12963T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17040623 | ||||||
| chr8:17040672
|
C | T | 75 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0297others(72): Show | 75 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.381+13012C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17040672 | ||||||
| chr8:17041091
|
A | G | 1 | a0001c0001t0015g0319 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.381+13431A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041091 | ||||||
| chr8:17041114
|
C | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+13454C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041114 | ||||||
| chr8:17041208
|
T | G | 362 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(359): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.381+13548T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041208 | ||||||
| chr8:17041311
|
A | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+13651A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041311 | ||||||
| chr8:17041352
|
C | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+13692C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041352 | ||||||
| chr8:17041438
|
G | T | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.381+13778G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041438 | ||||||
| chr8:17041445
|
T | C | 1 | a0001c0001t0005g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.381+13785T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041445 | ||||||
| chr8:17041469
|
T | C | 4 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0002g0348others(1): Show | 4 | NA18949.hp1 NA19004.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+13809T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041469 | ||||||
| chr8:17041536
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.381+13876A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041536 | ||||||
| chr8:17041569
|
A | G | 1 | a0001c0001t0002g0163 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.381+13909A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041569 | ||||||
| chr8:17041626
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.381+13966G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041626 | ||||||
| chr8:17041630
|
T | G | 1 | a0001c0001t0002g0329 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.381+13970T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041630 | ||||||
| chr8:17041671
|
G | A | 167 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(164): Show | 172 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.381+14011G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041671 | ||||||
| chr8:17041676
|
T | C | 6 | a0001c0001t0001g0326a0001c0004t0001g0209a0001c0004t0002g0208others(3): Show | 6 | HG00438.hp1 HG02074.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+14016T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041676 | ||||||
| chr8:17041766
|
G | C | 3 | a0002c0002t0008g0172a0002c0002t0008g0176a0002c0002t0008g0177 | 3 | HG02486.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.381+14106G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041766 | ||||||
| chr8:17041766
|
G | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(15): Show | 18 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.381+14106G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041766 | ||||||
| chr8:17041896
|
G | A | 29 | a0002c0002t0001g0003a0002c0002t0001g0178a0002c0002t0001g0179others(26): Show | 30 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.381+14236G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041896 | ||||||
| chr8:17041918
|
G | A | 4 | a0001c0001t0001g0228a0001c0001t0001g0232a0001c0001t0013g0224others(1): Show | 4 | HG03490.hp2 HG03669.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+14258G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17041918 | ||||||
| chr8:17042066
|
C | G | 1 | a0001c0001t0002g0162 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.381+14406C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042066 | ||||||
| chr8:17042103
|
T | G | 1 | a0001c0001t0003g0072 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.381+14443T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042103 | ||||||
| chr8:17042151
|
G | A | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.381+14491G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042151 | ||||||
| chr8:17042271
|
C | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0236others(31): Show | 36 | HG01243.hp1 HG01361.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.381+14611C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042271 | ||||||
| chr8:17042423
|
T | C | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+14763T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042423 | ||||||
| chr8:17042524
|
C | G | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.381+14864C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042524 | ||||||
| chr8:17042615
|
G | A | 1 | a0001c0001t0004g0248 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.381+14955G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042615 | ||||||
| chr8:17042724
|
C | T | 172 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(169): Show | 177 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.381+15064C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042724 | ||||||
| chr8:17042729
|
C | T | 73 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0297others(70): Show | 73 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.381+15069C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042729 | ||||||
| chr8:17042730
|
C | G | 214 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(211): Show | 221 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.381+15070C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042730 | ||||||
| chr8:17042734
|
T | G | 3 | a0002c0002t0001g0192a0002c0002t0001g0195a0002c0002t0001g0196 | 3 | HG02257.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.381+15074T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042734 | ||||||
| chr8:17042900
|
T | C | 7 | a0001c0001t0001g0048a0001c0001t0001g0070a0001c0001t0002g0001others(4): Show | 8 | HG00639.hp1 HG01081.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+15240T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042900 | ||||||
| chr8:17042921
|
A | T | 1 | a0001c0001t0001g0323 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.381+15261A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042921 | ||||||
| chr8:17042929
|
T | G | 2 | a0001c0001t0002g0360a0001c0001t0002g0361 | 2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.381+15269T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042929 | ||||||
| chr8:17042931
|
A | AT | 82 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0048others(79): Show | 85 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.381+15297dupT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17042931 | |||||
| chr8:17042931
|
A | ATT | 66 | a0001c0001t0001g0173a0001c0001t0001g0293a0001c0001t0001g0297others(63): Show | 66 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.381+15296_381+1529 others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17042931 | |||||
| chr8:17042931
|
A | ATTT | 41 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0213others(38): Show | 44 | HG00438.hp1 HG00544.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.381+15295_381+1529 others(7): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17042931 | |||||
| chr8:17042931
|
A | ATTTT | 20 | a0001c0001t0001g0016a0001c0001t0001g0212a0001c0001t0001g0326others(17): Show | 20 | HG01109.hp2 HG02074.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.381+15294_381+1529 others(8): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17042931 | |||||
| chr8:17042931
|
A | ATTTTT | 12 | a0001c0001t0001g0026a0001c0001t0001g0286a0001c0001t0006g0015others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.381+15293_381+1529 others(9): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17042931 | |||||
| chr8:17042931
|
A | ATTTTTT | 14 | a0001c0001t0006g0014a0002c0002t0001g0178a0002c0002t0001g0179others(11): Show | 14 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.381+15292_381+1529 others(10): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17042931 | |||||
| chr8:17042931
|
A | ATTTTTTT | 8 | a0001c0001t0025g0018a0002c0002t0001g0003a0002c0002t0001g0191others(5): Show | 9 | HG02572.hp1 HG02647.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+15291_381+1529 others(11): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17042931 | |||||
| chr8:17042931
|
A | ATTTTTTT others(3): Show |
2 | a0002c0002t0008g0172a0002c0002t0008g0176 | 2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.381+15288_381+1529 others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17042931 | |||||
| chr8:17042931
|
A | ATTTTTTT others(5): Show |
1 | a0002c0002t0008g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.381+15286_381+1529 others(16): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17042931 | |||||
| chr8:17042931
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.381+15286_381+1529 others(16): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17042931 | |||||
| chr8:17042963
|
G | A | 12 | a0001c0003t0002g0039a0001c0003t0002g0054a0001c0003t0002g0200others(9): Show | 12 | HG00639.hp2 HG00735.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.381+15303G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17042963 | ||||||
| chr8:17043084
|
C | T | 44 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0205others(41): Show | 46 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.381+15424C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043084 | ||||||
| chr8:17043133
|
G | T | 1 | a0001c0001t0002g0318 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.381+15473G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043133 | ||||||
| chr8:17043186
|
G | A | 1 | a0001c0001t0003g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.381+15526G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043186 | ||||||
| chr8:17043202
|
T | G | 44 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0205others(41): Show | 46 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.381+15542T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043202 | ||||||
| chr8:17043203
|
G | T | 44 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0205others(41): Show | 46 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.381+15543G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043203 | ||||||
| chr8:17043210
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.381+15550A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043210 | ||||||
| chr8:17043223
|
G | A | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.381+15563G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043223 | ||||||
| chr8:17043270
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.381+15610A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043270 | ||||||
| chr8:17043283
|
C | G | 17 | a0001c0001t0001g0082a0001c0001t0001g0125a0001c0001t0001g0126others(14): Show | 17 | HG00438.hp2 HG01433.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.381+15623C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043283 | ||||||
| chr8:17043356
|
A | T | 1 | a0001c0001t0013g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.381+15696A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043356 | ||||||
| chr8:17043428
|
A | G | 1 | a0001c0001t0002g0275 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.381+15768A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043428 | ||||||
| chr8:17043536
|
G | A | 6 | a0001c0001t0002g0329a0001c0001t0002g0330a0001c0001t0002g0331others(3): Show | 6 | NA18952.hp1 NA18953.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+15876G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043536 | ||||||
| chr8:17043557
|
T | C | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(99): Show | 102 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.381+15897T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043557 | ||||||
| chr8:17043567
|
C | T | 44 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0205others(41): Show | 46 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.381+15907C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043567 | ||||||
| chr8:17043591
|
C | A | 1 | a0001c0001t0003g0099 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.381+15931C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043591 | ||||||
| chr8:17043884
|
G | A | 1 | a0001c0001t0003g0134 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.381+16224G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043884 | ||||||
| chr8:17043886
|
A | C | 1 | a0001c0001t0006g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.381+16226A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17043886 | ||||||
| chr8:17044110
|
C | T | 17 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0128others(14): Show | 18 | HG00438.hp2 HG01256.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.381+16450C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044110 | ||||||
| chr8:17044166
|
G | C | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+16506G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044166 | ||||||
| chr8:17044267
|
G | C | 1 | a0001c0001t0001g0297 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.381+16607G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044267 | ||||||
| chr8:17044292
|
C | A | 167 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(164): Show | 173 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.381+16632C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044292 | ||||||
| chr8:17044404
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.381+16744G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044404 | ||||||
| chr8:17044554
|
T | C | 1 | a0001c0001t0003g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.381+16894T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044554 | ||||||
| chr8:17044703
|
T | G | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.381+17043T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044703 | ||||||
| chr8:17044790
|
T | C | 1 | a0001c0001t0003g0283 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.381+17130T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044790 | ||||||
| chr8:17044839
|
C | T | 2 | a0001c0001t0002g0360a0001c0001t0002g0361 | 2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.381+17179C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044839 | ||||||
| chr8:17044926
|
A | G | 3 | a0002c0002t0008g0172a0002c0002t0008g0176a0002c0002t0008g0177 | 3 | HG02486.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.381+17266A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044926 | ||||||
| chr8:17044938
|
A | G | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+17278A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17044938 | ||||||
| chr8:17045003
|
G | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(21): Show | 27 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+17343G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045003 | ||||||
| chr8:17045076
|
A | G | 24 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(21): Show | 27 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+17416A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045076 | ||||||
| chr8:17045081
|
C | T | 1 | a0001c0001t0002g0333 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.381+17421C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045081 | ||||||
| chr8:17045082
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.381+17422G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045082 | ||||||
| chr8:17045228
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.381+17568G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045228 | ||||||
| chr8:17045298
|
C | T | 1 | a0001c0001t0002g0252 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.381+17638C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045298 | ||||||
| chr8:17045465
|
T | G | 93 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0173others(90): Show | 97 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.381+17805T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045465 | ||||||
| chr8:17045563
|
G | C | 1 | a0001c0001t0001g0346 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.381+17903G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045563 | ||||||
| chr8:17045635
|
G | T | 1 | a0001c0001t0002g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.381+17975G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045635 | ||||||
| chr8:17045821
|
G | A | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381+18161G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045821 | ||||||
| chr8:17045929
|
G | T | 1 | a0001c0001t0002g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.382-18155G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045929 | ||||||
| chr8:17045939
|
C | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0205others(38): Show | 43 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.382-18145C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17045939 | ||||||
| chr8:17046099
|
C | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.382-17985C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046099 | ||||||
| chr8:17046124
|
T | A | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-17960T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046124 | ||||||
| chr8:17046179
|
G | T | 1 | a0001c0001t0013g0224 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.382-17905G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046179 | ||||||
| chr8:17046201
|
G | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(211): Show | 221 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.382-17883G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046201 | ||||||
| chr8:17046282
|
A | C | 1 | a0001c0003t0007g0036 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.382-17802A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046282 | ||||||
| chr8:17046417
|
G | A | 1 | a0002c0002t0001g0364 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.382-17667G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046417 | ||||||
| chr8:17046436
|
C | T | 169 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(166): Show | 174 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.382-17648C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046436 | ||||||
| chr8:17046488
|
A | G | 1 | a0001c0001t0002g0289 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.382-17596A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046488 | ||||||
| chr8:17046571
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.382-17513A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046571 | ||||||
| chr8:17046598
|
G | C | 214 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(211): Show | 221 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.382-17486G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046598 | ||||||
| chr8:17046718
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(22): Show | 28 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.382-17366C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046718 | ||||||
| chr8:17046730
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0216 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.382-17354C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046730 | ||||||
| chr8:17046731
|
G | A | 88 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0173others(85): Show | 92 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.382-17353G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046731 | ||||||
| chr8:17046758
|
C | T | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-17326C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046758 | ||||||
| chr8:17046940
|
A | G | 2 | a0001c0001t0003g0002a0001c0001t0003g0149 | 3 | NA18942.hp1 NA18963.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.382-17144A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17046940 | ||||||
| chr8:17047014
|
G | A | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-17070G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047014 | ||||||
| chr8:17047124
|
C | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(211): Show | 221 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.382-16960C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047124 | ||||||
| chr8:17047244
|
C | T | 44 | a0001c0001t0001g0082a0001c0001t0002g0252a0001c0001t0002g0275others(41): Show | 46 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.382-16840C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047244 | ||||||
| chr8:17047255
|
A | G | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-16829A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047255 | ||||||
| chr8:17047306
|
G | T | 1 | a0001c0001t0002g0342 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.382-16778G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047306 | ||||||
| chr8:17047517
|
C | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0005g0027others(15): Show | 18 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.382-16567C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047517 | ||||||
| chr8:17047614
|
C | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.382-16470C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047614 | ||||||
| chr8:17047626
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.382-16458C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047626 | ||||||
| chr8:17047690
|
T | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.382-16394T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047690 | ||||||
| chr8:17047777
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.382-16307C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047777 | ||||||
| chr8:17047996
|
C | T | 1 | a0004c0010t0002g0280 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.382-16088C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17047996 | ||||||
| chr8:17048014
|
G | A | 3 | a0001c0001t0003g0002a0001c0001t0003g0146a0001c0001t0003g0149 | 4 | NA18942.hp1 NA18963.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-16070G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048014 | ||||||
| chr8:17048016
|
C | T | 88 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0173others(85): Show | 92 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.382-16068C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048016 | ||||||
| chr8:17048284
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.382-15800C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048284 | ||||||
| chr8:17048310
|
T | C | 82 | a0001c0001t0001g0286a0001c0001t0001g0293a0001c0001t0001g0294others(79): Show | 82 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.382-15774T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048310 | ||||||
| chr8:17048326
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0121others(4): Show | 7 | HG00408.hp2 HG01884.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.382-15758C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048326 | ||||||
| chr8:17048327
|
G | A | 213 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(210): Show | 220 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.382-15757G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048327 | ||||||
| chr8:17048420
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.382-15664C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048420 | ||||||
| chr8:17048482
|
A | G | 1 | a0001c0001t0004g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.382-15602A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048482 | ||||||
| chr8:17048539
|
T | C | 42 | a0001c0001t0001g0082a0001c0001t0002g0252a0001c0001t0002g0275others(39): Show | 44 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.382-15545T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048539 | ||||||
| chr8:17048586
|
T | C | 1 | a0001c0001t0004g0256 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.382-15498T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048586 | ||||||
| chr8:17048588
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0205 | 3 | HG02809.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.382-15496G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048588 | ||||||
| chr8:17048652
|
G | T | 29 | a0002c0002t0001g0003a0002c0002t0001g0178a0002c0002t0001g0179others(26): Show | 30 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.382-15432G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048652 | ||||||
| chr8:17048791
|
A | T | 101 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(98): Show | 101 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.382-15293A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048791 | ||||||
| chr8:17048895
|
C | T | 2 | a0002c0002t0001g0183a0002c0002t0001g0185 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.382-15189C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048895 | ||||||
| chr8:17048896
|
G | A | 1 | a0001c0001t0003g0072 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.382-15188G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17048896 | ||||||
| chr8:17049013
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.382-15071G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049013 | ||||||
| chr8:17049038
|
C | G | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-15046C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049038 | ||||||
| chr8:17049058
|
C | T | 1 | a0004c0010t0002g0280 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.382-15026C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049058 | ||||||
| chr8:17049059
|
G | A | 1 | a0003c0007t0002g0064 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.382-15025G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049059 | ||||||
| chr8:17049122
|
C | T | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.382-14962C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049122 | ||||||
| chr8:17049150
|
A | G | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-14934A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049150 | ||||||
| chr8:17049236
|
G | A | 5 | a0001c0001t0001g0121a0001c0001t0003g0059a0001c0001t0003g0063others(2): Show | 5 | HG00408.hp2 NA18950.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-14848G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049236 | ||||||
| chr8:17049324
|
C | T | 3 | a0001c0001t0004g0009a0001c0001t0004g0248a0001c0001t0004g0266 | 4 | NA18953.hp1 NA18990.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-14760C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049324 | ||||||
| chr8:17049328
|
T | G | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.382-14756T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049328 | ||||||
| chr8:17049616
|
G | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0026others(184): Show | 191 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.382-14468G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049616 | ||||||
| chr8:17049683
|
A | T | 1 | a0001c0001t0002g0151 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.382-14401A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049683 | ||||||
| chr8:17049800
|
A | G | 16 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0128others(13): Show | 16 | HG00438.hp2 HG01433.hp2 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.382-14284A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049800 | ||||||
| chr8:17049808
|
T | A | 100 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(97): Show | 100 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.382-14276T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049808 | ||||||
| chr8:17049971
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0220 | 3 | NA18951.hp2 NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.382-14113C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17049971 | ||||||
| chr8:17050103
|
C | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.382-13981C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17050103 | ||||||
| chr8:17050110
|
G | A | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-13974G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17050110 | ||||||
| chr8:17050198
|
C | T | 1 | a0001c0001t0003g0148 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.382-13886C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17050198 | ||||||
| chr8:17050509
|
G | A | 187 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(184): Show | 192 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.382-13575G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17050509 | ||||||
| chr8:17050663
|
T | C | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-13421T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17050663 | ||||||
| chr8:17050719
|
C | T | 4 | a0001c0001t0002g0060a0001c0001t0002g0150a0001c0001t0002g0153others(1): Show | 4 | HG00438.hp2 HG01433.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-13365C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17050719 | ||||||
| chr8:17050846
|
C | G | 1 | a0001c0001t0001g0037 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.382-13238C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17050846 | ||||||
| chr8:17051027
|
C | G | 3 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0313 | 3 | HG01257.hp1 HG01258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.382-13057C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17051027 | ||||||
| chr8:17051032
|
A | G | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.382-13052A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17051032 | ||||||
| chr8:17051188
|
T | G | 4 | a0001c0001t0008g0011a0002c0002t0008g0172a0002c0002t0008g0176others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-12896T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17051188 | ||||||
| chr8:17051199
|
A | T | 1 | a0002c0002t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.382-12885A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17051199 | ||||||
| chr8:17051201
|
G | GTACTAAT others(10): Show |
1 | a0002c0002t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.382-12881_382-1288 others(21): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17051201 | |||||
| chr8:17051248
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0220 | 3 | NA18951.hp2 NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.382-12836T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17051248 | ||||||
| chr8:17051375
|
G | T | 8 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0193others(5): Show | 8 | HG02257.hp2 HG02886.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-12709G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17051375 | ||||||
| chr8:17051386
|
A | T | 1 | a0002c0005t0001g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.382-12698A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17051386 | ||||||
| chr8:17051479
|
A | T | 100 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(97): Show | 100 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.382-12605A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17051479 | ||||||
| chr8:17051532
|
G | A | 16 | a0001c0001t0001g0167a0001c0003t0002g0039a0001c0003t0002g0054others(13): Show | 16 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.382-12552G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17051532 | ||||||
| chr8:17051741
|
G | T | 1 | a0001c0001t0002g0151 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.382-12343G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17051741 | ||||||
| chr8:17052138
|
G | T | 33 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235others(30): Show | 34 | HG01243.hp1 HG01361.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.382-11946G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052138 | ||||||
| chr8:17052163
|
C | T | 4 | a0001c0001t0008g0011a0002c0002t0008g0172a0002c0002t0008g0176others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-11921C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052163 | ||||||
| chr8:17052221
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.382-11863A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052221 | ||||||
| chr8:17052222
|
T | A | 226 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(223): Show | 233 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.382-11862T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052222 | ||||||
| chr8:17052237
|
T | A | 7 | a0001c0001t0001g0326a0001c0001t0001g0351a0001c0004t0001g0209others(4): Show | 7 | HG00438.hp1 HG02074.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-11847T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052237 | ||||||
| chr8:17052240
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.382-11844G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052240 | ||||||
| chr8:17052243
|
T | C | 1 | a0001c0001t0003g0062 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.382-11841T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052243 | ||||||
| chr8:17052257
|
G | A | 226 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(223): Show | 233 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.382-11827G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052257 | ||||||
| chr8:17052313
|
G | C | 1 | a0001c0001t0001g0326 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.382-11771G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052313 | ||||||
| chr8:17052387
|
G | A | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.382-11697G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052387 | ||||||
| chr8:17052450
|
A | T | 1 | a0001c0001t0012g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.382-11634A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052450 | ||||||
| chr8:17052670
|
G | A | 362 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(359): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.382-11414G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052670 | ||||||
| chr8:17052840
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.382-11244C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17052840 | ||||||
| chr8:17053070
|
G | A | 1 | a0001c0006t0001g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.382-11014G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053070 | ||||||
| chr8:17053093
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.382-10991A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053093 | ||||||
| chr8:17053184
|
GGTAAGGT others(10): Show |
G | 1 | a0001c0001t0002g0127 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.382-10883_382-1086 others(21): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17053184 | |||||
| chr8:17053220
|
T | C | 1 | a0001c0001t0003g0057 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.382-10864T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053220 | ||||||
| chr8:17053270
|
C | T | 2 | a0001c0001t0002g0360a0001c0001t0002g0361 | 2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.382-10814C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053270 | ||||||
| chr8:17053279
|
G | A | 1 | a0001c0001t0008g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.382-10805G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053279 | ||||||
| chr8:17053383
|
C | G | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.382-10701C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053383 | ||||||
| chr8:17053393
|
C | T | 1 | a0004c0010t0002g0280 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.382-10691C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053393 | ||||||
| chr8:17053496
|
T | C | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.382-10588T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053496 | ||||||
| chr8:17053654
|
T | A | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.382-10430T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053654 | ||||||
| chr8:17053735
|
G | A | 2 | a0001c0006t0001g0237a0001c0006t0001g0239 | 2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.382-10349G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053735 | ||||||
| chr8:17053744
|
C | T | 1 | a0001c0001t0004g0265 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.382-10340C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053744 | ||||||
| chr8:17053797
|
G | A | 1 | a0001c0001t0018g0233 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.382-10287G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053797 | ||||||
| chr8:17053851
|
G | A | 57 | a0001c0001t0001g0082a0001c0001t0002g0252a0001c0001t0002g0275others(54): Show | 59 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.382-10233G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053851 | ||||||
| chr8:17053858
|
C | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(21): Show | 27 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.382-10226C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053858 | ||||||
| chr8:17053909
|
A | G | 57 | a0001c0001t0001g0082a0001c0001t0002g0252a0001c0001t0002g0275others(54): Show | 59 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.382-10175A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053909 | ||||||
| chr8:17053980
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.382-10104T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053980 | ||||||
| chr8:17053986
|
T | C | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.382-10098T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17053986 | ||||||
| chr8:17054003
|
C | A | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.382-10081C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054003 | ||||||
| chr8:17054024
|
G | C | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.382-10060G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054024 | ||||||
| chr8:17054057
|
G | A | 46 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0205others(43): Show | 48 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.382-10027G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054057 | ||||||
| chr8:17054196
|
A | G | 1 | a0001c0001t0005g0226 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.382-9888A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054196 | ||||||
| chr8:17054197
|
T | C | 1 | a0001c0004t0001g0350 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.382-9887T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054197 | ||||||
| chr8:17054357
|
G | C | 1 | a0001c0001t0006g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.382-9727G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054357 | ||||||
| chr8:17054474
|
T | C | 3 | a0001c0001t0002g0252a0001c0001t0004g0068a0001c0001t0004g0265 | 3 | HG03942.hp2 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.382-9610T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054474 | ||||||
| chr8:17054738
|
C | CT | 86 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0122others(83): Show | 88 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.382-9327dupT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17054738 | |||||
| chr8:17054738
|
C | CTT | 76 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0297others(73): Show | 78 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.382-9328_382-9327d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17054738 | |||||
| chr8:17054738
|
CTTT | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0205others(42): Show | 47 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.382-9329_382-9327d others(5): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17054738 | |||||
| chr8:17054778
|
C | T | 1 | a0001c0001t0002g0145 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.382-9306C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054778 | ||||||
| chr8:17054878
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.382-9206A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054878 | ||||||
| chr8:17054903
|
T | C | 1 | a0001c0001t0002g0060 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.382-9181T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054903 | ||||||
| chr8:17054964
|
C | T | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.382-9120C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17054964 | ||||||
| chr8:17055024
|
A | G | 1 | a0001c0001t0003g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.382-9060A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17055024 | ||||||
| chr8:17055146
|
C | T | 230 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(227): Show | 237 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.382-8938C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17055146 | ||||||
| chr8:17055169
|
G | C | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.382-8915G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17055169 | ||||||
| chr8:17055194
|
A | G | 1 | a0001c0001t0002g0349 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.382-8890A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17055194 | ||||||
| chr8:17055264
|
CAAT | C | 36 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235others(33): Show | 37 | HG01243.hp1 HG01361.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.382-8819_382-8817d others(5): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17055264 | ||||||
| chr8:17055369
|
A | C | 1 | a0001c0001t0002g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.382-8715A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17055369 | ||||||
| chr8:17055460
|
C | G | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.382-8624C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17055460 | ||||||
| chr8:17055483
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0070a0001c0001t0002g0001 | 4 | HG00639.hp1 HG01081.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-8601T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17055483 | ||||||
| chr8:17055665
|
G | A | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-8419G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17055665 | ||||||
| chr8:17055773
|
T | A | 1 | a0001c0001t0003g0147 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.382-8311T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17055773 | ||||||
| chr8:17056117
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.382-7967A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17056117 | ||||||
| chr8:17056268
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0045 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.382-7816A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17056268 | ||||||
| chr8:17056322
|
A | T | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.382-7762A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17056322 | ||||||
| chr8:17056495
|
A | T | 3 | a0001c0001t0002g0013a0001c0001t0002g0312a0001c0001t0002g0317 | 3 | HG00544.hp1 HG00621.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.382-7589A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17056495 | ||||||
| chr8:17056591
|
C | T | 50 | a0001c0001t0001g0082a0001c0001t0002g0252a0001c0001t0002g0275others(47): Show | 52 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.382-7493C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17056591 | ||||||
| chr8:17056901
|
C | T | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-7183C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17056901 | ||||||
| chr8:17056902
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.382-7182G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17056902 | ||||||
| chr8:17056902
|
G | C | 81 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0294others(78): Show | 83 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.382-7182G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17056902 | ||||||
| chr8:17057010
|
C | G | 49 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(46): Show | 51 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.382-7074C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17057010 | ||||||
| chr8:17057025
|
C | T | 49 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(46): Show | 51 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.382-7059C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17057025 | ||||||
| chr8:17057039
|
A | T | 49 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(46): Show | 51 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.382-7045A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17057039 | ||||||
| chr8:17057461
|
G | T | 6 | a0001c0001t0002g0067a0001c0001t0002g0096a0001c0001t0002g0110others(3): Show | 6 | HG01069.hp1 HG02280.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-6623G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17057461 | ||||||
| chr8:17057819
|
G | A | 23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(20): Show | 23 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.382-6265G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17057819 | ||||||
| chr8:17057835
|
C | CTTG | 74 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0294others(71): Show | 75 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.382-6221_382-6219d others(5): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17057835 | |||||
| chr8:17057835
|
C | CTTGTTG | 3 | a0001c0001t0002g0290a0001c0001t0003g0288a0001c0001t0003g0291 | 3 | HG00099.hp2 HG01255.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.382-6224_382-6219d others(8): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17057835 | |||||
| chr8:17057835
|
C | CTTGTTGT others(5): Show |
1 | a0001c0001t0003g0292 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.382-6230_382-6219d others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17057835 | |||||
| chr8:17057974
|
A | C | 2 | a0001c0001t0001g0232a0001c0001t0018g0233 | 2 | HG03490.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.382-6110A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17057974 | ||||||
| chr8:17057996
|
C | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.382-6088C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17057996 | ||||||
| chr8:17058081
|
C | G | 1 | a0001c0001t0004g0265 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.382-6003C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058081 | ||||||
| chr8:17058082
|
G | A | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-6002G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058082 | ||||||
| chr8:17058139
|
C | T | 157 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(154): Show | 159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.382-5945C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058139 | ||||||
| chr8:17058163
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.382-5921A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058163 | ||||||
| chr8:17058255
|
G | A | 157 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(154): Show | 159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.382-5829G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058255 | ||||||
| chr8:17058266
|
T | G | 7 | a0001c0001t0004g0247a0001c0001t0004g0250a0001c0001t0004g0256others(4): Show | 7 | NA18954.hp2 NA18964.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.382-5818T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058266 | ||||||
| chr8:17058294
|
C | T | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-5790C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058294 | ||||||
| chr8:17058319
|
G | C | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(99): Show | 102 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.382-5765G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058319 | ||||||
| chr8:17058355
|
A | T | 2 | a0001c0001t0004g0343a0001c0001t0016g0338 | 2 | NA18974.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.382-5729A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058355 | ||||||
| chr8:17058391
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.382-5693C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058391 | ||||||
| chr8:17058405
|
C | G | 4 | a0002c0002t0001g0178a0002c0002t0008g0172a0002c0002t0008g0176others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-5679C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058405 | ||||||
| chr8:17058471
|
G | T | 55 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(52): Show | 57 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.382-5613G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058471 | ||||||
| chr8:17058491
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0205 | 3 | HG02809.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.382-5593A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058491 | ||||||
| chr8:17058532
|
G | T | 1 | a0001c0001t0003g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.382-5552G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058532 | ||||||
| chr8:17058854
|
G | A | 283 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(280): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.382-5230G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17058854 | ||||||
| chr8:17059054
|
G | A | 2 | a0001c0001t0003g0135a0001c0001t0016g0088 | 2 | NA18979.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.382-5030G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059054 | ||||||
| chr8:17059178
|
G | T | 101 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(98): Show | 101 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.382-4906G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059178 | ||||||
| chr8:17059262
|
C | T | 101 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(98): Show | 101 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.382-4822C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059262 | ||||||
| chr8:17059327
|
A | T | 1 | a0001c0001t0002g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.382-4757A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059327 | ||||||
| chr8:17059479
|
T | C | 103 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(100): Show | 104 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.382-4605T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059479 | ||||||
| chr8:17059511
|
G | T | 143 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(140): Show | 145 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.382-4573G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059511 | ||||||
| chr8:17059561
|
A | T | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.382-4523A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059561 | ||||||
| chr8:17059701
|
C | T | 1 | a0001c0001t0025g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-4383C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059701 | ||||||
| chr8:17059741
|
A | G | 4 | a0001c0001t0001g0228a0001c0001t0001g0232a0001c0001t0013g0224others(1): Show | 4 | HG03490.hp2 HG03669.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-4343A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059741 | ||||||
| chr8:17059790
|
T | A | 1 | a0001c0003t0011g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.382-4294T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059790 | ||||||
| chr8:17059802
|
A | G | 1 | a0001c0001t0004g0157 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.382-4282A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059802 | ||||||
| chr8:17059854
|
A | G | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-4230A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059854 | ||||||
| chr8:17059951
|
T | A | 4 | a0001c0001t0001g0359a0001c0001t0002g0360a0001c0001t0002g0361others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-4133T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059951 | ||||||
| chr8:17059995
|
T | G | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-4089T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17059995 | ||||||
| chr8:17060136
|
A | G | 1 | a0001c0001t0003g0101 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.382-3948A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060136 | ||||||
| chr8:17060170
|
A | G | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.382-3914A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060170 | ||||||
| chr8:17060296
|
CT | C | 123 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0168others(120): Show | 129 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.382-3774delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17060296 | |||||
| chr8:17060373
|
T | C | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.382-3711T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060373 | ||||||
| chr8:17060394
|
T | G | 1 | a0001c0001t0012g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.382-3690T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060394 | ||||||
| chr8:17060395
|
A | T | 283 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(280): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.382-3689A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060395 | ||||||
| chr8:17060476
|
C | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.382-3608C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060476 | ||||||
| chr8:17060508
|
C | T | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.382-3576C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060508 | ||||||
| chr8:17060554
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.382-3530C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060554 | ||||||
| chr8:17060555
|
G | A | 25 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0002g0013others(22): Show | 25 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.382-3529G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060555 | ||||||
| chr8:17060587
|
C | T | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-3497C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060587 | ||||||
| chr8:17060588
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.382-3496G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060588 | ||||||
| chr8:17060701
|
A | G | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-3383A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060701 | ||||||
| chr8:17060801
|
AT | A | 94 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(91): Show | 99 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.382-3268delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17060801 | |||||
| chr8:17060906
|
G | A | 3 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.382-3178G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17060906 | ||||||
| chr8:17061038
|
A | G | 1 | a0001c0003t0002g0201 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.382-3046A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17061038 | ||||||
| chr8:17061441
|
T | A | 212 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(209): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.382-2643T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17061441 | ||||||
| chr8:17061577
|
C | T | 47 | a0001c0001t0002g0141a0001c0001t0003g0002a0001c0001t0003g0057others(44): Show | 48 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.382-2507C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17061577 | ||||||
| chr8:17061615
|
G | A | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.382-2469G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17061615 | ||||||
| chr8:17061823
|
C | T | 58 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(55): Show | 60 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.382-2261C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17061823 | ||||||
| chr8:17061894
|
G | T | 1 | a0001c0001t0003g0299 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.382-2190G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17061894 | ||||||
| chr8:17061981
|
G | A | 1 | a0001c0001t0023g0249 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.382-2103G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17061981 | ||||||
| chr8:17062119
|
T | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0236others(2): Show | 6 | HG01243.hp1 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-1965T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062119 | ||||||
| chr8:17062133
|
A | C | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.382-1951A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062133 | ||||||
| chr8:17062192
|
C | G | 57 | a0001c0001t0001g0082a0001c0001t0002g0252a0001c0001t0002g0275others(54): Show | 59 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.382-1892C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062192 | ||||||
| chr8:17062200
|
G | A | 77 | a0001c0001t0001g0121a0001c0001t0001g0144a0001c0001t0001g0293others(74): Show | 77 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.382-1884G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062200 | ||||||
| chr8:17062258
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0003g0056 | 2 | HG01975.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.382-1826C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062258 | ||||||
| chr8:17062282
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.382-1802A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062282 | ||||||
| chr8:17062314
|
G | T | 3 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0003g0357 | 3 | HG03130.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.382-1770G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062314 | ||||||
| chr8:17062460
|
C | G | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(99): Show | 102 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.382-1624C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062460 | ||||||
| chr8:17062535
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.382-1549A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062535 | ||||||
| chr8:17062618
|
T | C | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.382-1466T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062618 | ||||||
| chr8:17062837
|
C | T | 79 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0294others(76): Show | 79 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.382-1247C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062837 | ||||||
| chr8:17062958
|
T | G | 64 | a0001c0001t0001g0070a0001c0001t0001g0168a0001c0001t0001g0170others(61): Show | 66 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.382-1126T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17062958 | ||||||
| chr8:17063120
|
G | A | 30 | a0001c0001t0011g0322a0002c0002t0001g0003a0002c0002t0001g0178others(27): Show | 31 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.382-964G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17063120 | ||||||
| chr8:17063135
|
T | C | 190 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0070others(187): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.382-949T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17063135 | ||||||
| chr8:17063136
|
G | C | 58 | a0001c0001t0001g0082a0001c0001t0002g0034a0001c0001t0002g0252others(55): Show | 60 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.382-948G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17063136 | ||||||
| chr8:17063228
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.382-856G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17063228 | ||||||
| chr8:17063511
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0205 | 3 | HG02809.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.382-573A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17063511 | ||||||
| chr8:17063623
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.382-461G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17063623 | ||||||
| chr8:17063646
|
AT | A | 56 | a0001c0001t0002g0252a0001c0001t0002g0275a0001c0001t0002g0277others(53): Show | 58 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.382-434delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 17063646 | |||||
| chr8:17063745
|
G | A | 1 | a0001c0001t0002g0035 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.382-339G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17063745 | ||||||
| chr8:17063880
|
A | C | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-204A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17063880 | ||||||
| chr8:17063902
|
A | T | 1 | a0001c0001t0028g0302 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.382-182A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17063902 | ||||||
| chr8:17064051
|
A | G | 6 | a0001c0001t0003g0059a0001c0001t0003g0063a0001c0001t0003g0097others(3): Show | 7 | HG00408.hp2 NA18957.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-33A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/14 | chr8 | 17064051 | ||||||
| chr8:17064307
|
G | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+70G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17064307 | ||||||
| chr8:17064381
|
G | C | 78 | a0001c0001t0001g0121a0001c0001t0001g0144a0001c0001t0001g0293others(75): Show | 79 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.535+144G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17064381 | ||||||
| chr8:17064394
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.535+157A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17064394 | ||||||
| chr8:17064406
|
C | A | 1 | a0001c0001t0003g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.535+169C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17064406 | ||||||
| chr8:17064504
|
C | A | 179 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0074others(176): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.535+267C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17064504 | ||||||
| chr8:17064654
|
A | G | 1 | a0001c0001t0004g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.535+417A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17064654 | ||||||
| chr8:17064705
|
A | T | 81 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0294others(78): Show | 82 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.535+468A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17064705 | ||||||
| chr8:17064827
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.535+590G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17064827 | ||||||
| chr8:17064902
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.535+665T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17064902 | ||||||
| chr8:17065103
|
T | G | 1 | a0001c0001t0002g0327 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.535+866T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17065103 | ||||||
| chr8:17065147
|
A | G | 1 | a0001c0001t0003g0101 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.535+910A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17065147 | ||||||
| chr8:17065269
|
C | T | 77 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0294others(74): Show | 78 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.535+1032C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17065269 | ||||||
| chr8:17065358
|
G | A | 6 | a0001c0001t0006g0015a0001c0001t0006g0021a0001c0001t0006g0025others(3): Show | 6 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.535+1121G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17065358 | ||||||
| chr8:17065451
|
G | A | 4 | a0001c0001t0008g0011a0002c0002t0008g0172a0002c0002t0008g0176others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+1214G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17065451 | ||||||
| chr8:17065490
|
C | A | 2 | a0001c0001t0014g0006a0001c0001t0014g0217 | 3 | HG02451.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.535+1253C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17065490 | ||||||
| chr8:17065517
|
T | C | 84 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0168others(81): Show | 88 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.535+1280T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17065517 | ||||||
| chr8:17065826
|
G | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.535+1589G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17065826 | ||||||
| chr8:17065911
|
A | C | 6 | a0001c0003t0007g0036a0001c0003t0007g0038a0001c0003t0007g0047others(3): Show | 6 | HG01928.hp1 HG02155.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.535+1674A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17065911 | ||||||
| chr8:17066003
|
T | C | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(99): Show | 103 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.535+1766T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066003 | ||||||
| chr8:17066072
|
CT | C | 103 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(100): Show | 104 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.535+1846delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066072 | |||||
| chr8:17066115
|
A | G | 1 | a0001c0001t0027g0169 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.535+1878A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066115 | ||||||
| chr8:17066151
|
A | C | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.535+1914A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066151 | ||||||
| chr8:17066185
|
T | C | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.535+1948T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066185 | ||||||
| chr8:17066390
|
A | G | 1 | a0001c0001t0006g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.535+2153A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066390 | ||||||
| chr8:17066392
|
G | C | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.535+2155G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066392 | ||||||
| chr8:17066514
|
A | AATATATA others(7): Show |
1 | a0001c0001t0003g0283 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.535+2279_535+2280i others(16): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066514 | |||||
| chr8:17066514
|
A | AATATATA others(9): Show |
2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.535+2279_535+2280i others(18): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066514 | |||||
| chr8:17066517
|
C | A | 3 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.535+2280C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066517 | ||||||
| chr8:17066517
|
C | CCA | 3 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0003t0001g0089 | 3 | HG00642.hp2 HG01123.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.535+2280_535+2281i others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066517 | ||||||
| chr8:17066517
|
C | CTA | 68 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0211others(65): Show | 71 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.535+2303_535+2304d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATA | 17 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(14): Show | 18 | HG00738.hp1 HG01257.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.535+2301_535+2304d others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATATA | 72 | a0001c0001t0001g0007a0001c0001t0001g0121a0001c0001t0001g0220others(69): Show | 74 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.535+2299_535+2304d others(8): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATATAT others(1): Show |
4 | a0001c0001t0001g0353a0001c0001t0002g0296a0001c0001t0002g0349others(1): Show | 4 | HG00099.hp2 HG00609.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+2297_535+2304d others(10): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATATAT others(3): Show |
2 | a0001c0001t0001g0223a0001c0001t0003g0215 | 2 | HG02738.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.535+2295_535+2304d others(12): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATATAT others(5): Show |
3 | a0001c0001t0003g0148a0001c0001t0004g0343a0001c0001t0016g0338 | 3 | NA18948.hp2 NA18974.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.535+2293_535+2304d others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATATAT others(9): Show |
4 | a0001c0001t0002g0341a0001c0001t0006g0025a0001c0001t0012g0029others(1): Show | 4 | HG02630.hp1 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+2289_535+2304d others(18): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATATAT others(11): Show |
3 | a0001c0001t0001g0355a0001c0001t0006g0017a0001c0001t0025g0018 | 3 | HG02886.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.535+2287_535+2304d others(20): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATATAT others(13): Show |
5 | a0001c0001t0001g0016a0001c0001t0001g0354a0001c0001t0010g0022others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+2285_535+2304d others(22): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATATAT others(15): Show |
5 | a0001c0001t0001g0356a0001c0001t0005g0027a0001c0001t0006g0015others(2): Show | 5 | HG02572.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+2283_535+2304d others(24): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATATAT others(17): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0286a0001c0001t0006g0021others(1): Show | 4 | HG02055.hp1 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.535+2281_535+2304d others(26): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
C | CTATATAT others(19): Show |
1 | a0001c0009t0001g0019 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.535+2304_535+2305i others(28): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066517
|
CTA | C | 71 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0041others(68): Show | 71 | HG00280.hp2 HG00597.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.535+2303_535+2304d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066517 | |||||
| chr8:17066523
|
A | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | NA18967.hp1 NA18985.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.535+2286A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066523 | ||||||
| chr8:17066530
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.535+2293T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066530 | ||||||
| chr8:17066532
|
T | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+2295T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066532 | ||||||
| chr8:17066534
|
T | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+2297T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066534 | ||||||
| chr8:17066536
|
T | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+2299T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066536 | ||||||
| chr8:17066538
|
T | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.535+2301T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066538 | ||||||
| chr8:17066540
|
T | G | 7 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0281others(4): Show | 7 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.535+2303T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066540 | ||||||
| chr8:17066542
|
G | T | 2 | a0001c0001t0006g0014a0001c0001t0025g0018 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.535+2305G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066542 | ||||||
| chr8:17066543
|
A | AT | 19 | a0001c0001t0001g0119a0001c0001t0002g0114a0001c0001t0002g0132others(16): Show | 19 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.535+2323dupT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066543 | |||||
| chr8:17066543
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0006g0014 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.535+2307_535+2308i others(23): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066543 | |||||
| chr8:17066543
|
AT | A | 124 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(121): Show | 129 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.535+2323delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066543 | |||||
| chr8:17066543
|
ATT | A | 79 | a0001c0001t0001g0121a0001c0001t0001g0168a0001c0001t0001g0170others(76): Show | 80 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.535+2322_535+2323d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17066543 | |||||
| chr8:17066585
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(23): Show | 28 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.535+2348C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066585 | ||||||
| chr8:17066606
|
G | A | 86 | a0001c0001t0001g0007a0001c0001t0001g0074a0001c0001t0001g0168others(83): Show | 89 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.535+2369G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066606 | ||||||
| chr8:17066608
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.535+2371T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066608 | ||||||
| chr8:17066698
|
A | C | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+2461A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066698 | ||||||
| chr8:17066734
|
A | G | 26 | a0001c0001t0011g0322a0002c0002t0001g0003a0002c0002t0001g0179others(23): Show | 27 | HG01175.hp1 HG01361.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.535+2497A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066734 | ||||||
| chr8:17066738
|
G | A | 2 | a0001c0001t0001g0167a0001c0003t0011g0061 | 2 | HG01123.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.535+2501G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066738 | ||||||
| chr8:17066927
|
G | C | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.535+2690G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066927 | ||||||
| chr8:17066982
|
T | A | 1 | a0001c0004t0004g0206 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.536-2706T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066982 | ||||||
| chr8:17066983
|
A | T | 1 | a0001c0004t0004g0206 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.536-2705A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17066983 | ||||||
| chr8:17067098
|
A | ACAATCAA others(7): Show |
5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.536-2584_536-2583i others(16): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17067098 | |||||
| chr8:17067182
|
T | G | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.536-2506T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17067182 | ||||||
| chr8:17067188
|
G | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0211a0001c0001t0001g0212others(18): Show | 23 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.536-2500G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17067188 | ||||||
| chr8:17067213
|
C | G | 1 | a0002c0002t0001g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.536-2475C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17067213 | ||||||
| chr8:17067287
|
TC | T | 15 | a0002c0002t0001g0003a0002c0002t0001g0179a0002c0002t0001g0182others(12): Show | 16 | HG01361.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.536-2400delC | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17067287 | ||||||
| chr8:17067430
|
A | AT | 7 | a0001c0001t0001g0074a0001c0001t0001g0126a0001c0001t0001g0359others(4): Show | 7 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.536-2244dupT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17067430 | |||||
| chr8:17067430
|
AT | A | 101 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(98): Show | 102 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.536-2244delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17067430 | |||||
| chr8:17067444
|
T | C | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.536-2244T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17067444 | ||||||
| chr8:17067483
|
G | A | 1 | a0001c0001t0002g0296 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.536-2205G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17067483 | ||||||
| chr8:17067521
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.536-2167C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17067521 | ||||||
| chr8:17067587
|
G | T | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-2101G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17067587 | ||||||
| chr8:17067872
|
C | T | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.536-1816C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17067872 | ||||||
| chr8:17067922
|
C | CTGAT | 289 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(286): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.536-1764_536-1763i others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 17067922 | |||||
| chr8:17067932
|
T | C | 2 | a0001c0001t0001g0352a0001c0001t0001g0353 | 2 | NA18963.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.536-1756T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17067932 | ||||||
| chr8:17068184
|
G | A | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(99): Show | 103 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.536-1504G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068184 | ||||||
| chr8:17068220
|
A | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0236others(33): Show | 38 | HG01175.hp1 HG01243.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.536-1468A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068220 | ||||||
| chr8:17068232
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.536-1456G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068232 | ||||||
| chr8:17068384
|
C | T | 285 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(282): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.536-1304C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068384 | ||||||
| chr8:17068429
|
T | C | 1 | a0001c0001t0010g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.536-1259T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068429 | ||||||
| chr8:17068455
|
C | T | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(99): Show | 103 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.536-1233C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068455 | ||||||
| chr8:17068670
|
A | G | 1 | a0001c0001t0004g0247 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.536-1018A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068670 | ||||||
| chr8:17068698
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.536-990G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068698 | ||||||
| chr8:17068737
|
A | C | 7 | a0001c0001t0001g0117a0001c0001t0002g0067a0001c0001t0002g0096others(4): Show | 7 | HG01069.hp1 HG01496.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.536-951A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068737 | ||||||
| chr8:17068837
|
G | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0013g0161 | 3 | HG00642.hp1 HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.536-851G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068837 | ||||||
| chr8:17068909
|
C | G | 1 | a0002c0002t0001g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.536-779C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068909 | ||||||
| chr8:17068991
|
G | T | 2 | a0001c0001t0003g0288a0001c0001t0003g0292 | 2 | HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.536-697G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17068991 | ||||||
| chr8:17069233
|
G | T | 1 | a0001c0001t0003g0062 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.536-455G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17069233 | ||||||
| chr8:17069255
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.536-433A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17069255 | ||||||
| chr8:17069446
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.536-242G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17069446 | ||||||
| chr8:17069492
|
G | A | 7 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0313others(4): Show | 7 | HG00741.hp2 HG01167.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.536-196G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17069492 | ||||||
| chr8:17069510
|
G | A | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(99): Show | 102 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.536-178G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17069510 | ||||||
| chr8:17069515
|
T | G | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.536-173T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 2/14 | chr8 | 17069515 | ||||||
| chr8:17069741
|
A | C | 57 | a0001c0001t0001g0082a0001c0001t0002g0252a0001c0001t0002g0275others(54): Show | 59 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.567+22A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17069741 | ||||||
| chr8:17069812
|
G | A | 1 | a0001c0001t0001g0351 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.567+93G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17069812 | ||||||
| chr8:17069902
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.567+183G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17069902 | ||||||
| chr8:17069905
|
C | T | 6 | a0001c0001t0001g0058a0001c0001t0001g0079a0001c0001t0001g0094others(3): Show | 6 | HG00099.hp1 HG00733.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.567+186C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17069905 | ||||||
| chr8:17069964
|
A | T | 1 | a0001c0001t0002g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.567+245A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17069964 | ||||||
| chr8:17070019
|
A | G | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.567+300A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070019 | ||||||
| chr8:17070035
|
C | T | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.567+316C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070035 | ||||||
| chr8:17070065
|
G | A | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(99): Show | 102 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.567+346G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070065 | ||||||
| chr8:17070183
|
G | A | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.567+464G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070183 | ||||||
| chr8:17070230
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.567+511A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070230 | ||||||
| chr8:17070279
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.567+560T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070279 | ||||||
| chr8:17070305
|
A | G | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.567+586A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070305 | ||||||
| chr8:17070368
|
A | C | 1 | a0001c0003t0020g0053 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.567+649A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070368 | ||||||
| chr8:17070526
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.567+807A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070526 | ||||||
| chr8:17070638
|
G | GA | 4 | a0001c0001t0001g0236a0001c0001t0002g0324a0001c0001t0005g0234others(1): Show | 4 | HG01243.hp1 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+919_567+920ins others(1): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070638 | ||||||
| chr8:17070638
|
GT | G | 56 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0041others(53): Show | 57 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.567+931delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17070638 | |||||
| chr8:17070639
|
T | A | 281 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(278): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.567+920T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070639 | ||||||
| chr8:17070640
|
T | A | 1 | a0001c0001t0006g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.567+921T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070640 | ||||||
| chr8:17070650
|
T | A | 2 | a0001c0001t0002g0324a0001c0001t0005g0027 | 2 | HG03041.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.567+931T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070650 | ||||||
| chr8:17070650
|
TA | T | 15 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0003g0059others(12): Show | 16 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.567+939delA | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17070650 | |||||
| chr8:17070651
|
A | T | 159 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0082others(156): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.567+932A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070651 | ||||||
| chr8:17070652
|
A | T | 56 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0141others(53): Show | 58 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.567+933A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070652 | ||||||
| chr8:17070653
|
A | T | 53 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0141others(50): Show | 55 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.567+934A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070653 | ||||||
| chr8:17070721
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.567+1002C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070721 | ||||||
| chr8:17070863
|
A | G | 1 | a0001c0001t0003g0210 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.567+1144A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070863 | ||||||
| chr8:17070877
|
G | A | 359 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(356): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.567+1158G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070877 | ||||||
| chr8:17070925
|
T | C | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.567+1206T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17070925 | ||||||
| chr8:17071059
|
C | A | 1 | a0001c0001t0002g0308 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.567+1340C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071059 | ||||||
| chr8:17071103
|
C | T | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.567+1384C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071103 | ||||||
| chr8:17071144
|
AG | A | 59 | a0001c0001t0001g0082a0001c0001t0002g0252a0001c0001t0002g0275others(56): Show | 61 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.567+1426delG | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071144 | ||||||
| chr8:17071340
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0011g0322others(25): Show | 30 | HG01175.hp1 HG01361.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.567+1621C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071340 | ||||||
| chr8:17071579
|
A | G | 2 | a0001c0001t0006g0014a0001c0001t0025g0018 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.567+1860A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071579 | ||||||
| chr8:17071640
|
C | T | 282 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(279): Show | 291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.567+1921C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071640 | ||||||
| chr8:17071678
|
A | G | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.567+1959A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071678 | ||||||
| chr8:17071686
|
T | G | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.567+1967T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071686 | ||||||
| chr8:17071826
|
A | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0013g0161 | 3 | HG00642.hp1 HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.567+2107A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071826 | ||||||
| chr8:17071935
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.567+2216G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071935 | ||||||
| chr8:17071989
|
A | G | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.567+2270A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17071989 | ||||||
| chr8:17072091
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.567+2372G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072091 | ||||||
| chr8:17072126
|
A | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0205others(96): Show | 103 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.567+2407A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072126 | ||||||
| chr8:17072176
|
T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0136 | 2 | HG01069.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.567+2457T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072176 | ||||||
| chr8:17072209
|
A | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.567+2490A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072209 | ||||||
| chr8:17072248
|
T | A | 92 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0205others(89): Show | 96 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.567+2529T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072248 | ||||||
| chr8:17072259
|
A | T | 1 | a0001c0001t0004g0271 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.567+2540A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072259 | ||||||
| chr8:17072274
|
A | C | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+2555A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072274 | ||||||
| chr8:17072333
|
G | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.567+2614G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072333 | ||||||
| chr8:17072426
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.567+2707T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072426 | ||||||
| chr8:17072454
|
GT | G | 28 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0074others(25): Show | 28 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.567+2748delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17072454 | |||||
| chr8:17072626
|
G | C | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.567+2907G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072626 | ||||||
| chr8:17072668
|
T | A | 286 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(283): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.567+2949T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072668 | ||||||
| chr8:17072758
|
G | A | 1 | a0002c0002t0001g0364 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.567+3039G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072758 | ||||||
| chr8:17072800
|
A | T | 1 | a0001c0001t0002g0151 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.567+3081A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072800 | ||||||
| chr8:17072832
|
C | T | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(99): Show | 103 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.567+3113C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072832 | ||||||
| chr8:17072870
|
A | G | 1 | a0001c0001t0003g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.567+3151A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072870 | ||||||
| chr8:17072956
|
T | C | 77 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0294others(74): Show | 78 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.567+3237T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17072956 | ||||||
| chr8:17073001
|
C | T | 1 | a0001c0001t0008g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.567+3282C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17073001 | ||||||
| chr8:17073121
|
T | C | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.567+3402T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17073121 | ||||||
| chr8:17073303
|
C | T | 1 | a0001c0001t0001g0353 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.567+3584C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17073303 | ||||||
| chr8:17073669
|
T | C | 1 | a0001c0011t0003g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.567+3950T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17073669 | ||||||
| chr8:17073705
|
T | C | 1 | a0001c0001t0002g0330 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.567+3986T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17073705 | ||||||
| chr8:17073753
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.568-4030A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17073753 | ||||||
| chr8:17073842
|
A | T | 2 | a0001c0001t0014g0006a0001c0001t0014g0217 | 3 | HG02451.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.568-3941A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17073842 | ||||||
| chr8:17074054
|
G | T | 4 | a0001c0001t0002g0132a0001c0001t0002g0154a0001c0001t0002g0155others(1): Show | 4 | HG00544.hp2 HG02040.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.568-3729G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074054 | ||||||
| chr8:17074055
|
G | T | 51 | a0001c0001t0002g0132a0001c0001t0002g0141a0001c0001t0002g0154others(48): Show | 52 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.568-3728G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074055 | ||||||
| chr8:17074169
|
A | T | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.568-3614A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074169 | ||||||
| chr8:17074182
|
A | G | 159 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.568-3601A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074182 | ||||||
| chr8:17074214
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.568-3569T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074214 | ||||||
| chr8:17074445
|
C | T | 76 | a0001c0001t0001g0007a0001c0001t0001g0168a0001c0001t0001g0170others(73): Show | 79 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.568-3338C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074445 | ||||||
| chr8:17074590
|
C | CAT | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.568-3193_568-3192i others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074590 | ||||||
| chr8:17074590
|
C | CGT | 71 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0049others(68): Show | 73 | HG00140.hp2 HG00597.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.568-3150_568-3149d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074590
|
C | CGTGT | 20 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 20 | HG00642.hp1 HG00735.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.568-3152_568-3149d others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074590
|
C | CGTGTGT | 5 | a0001c0001t0004g0068a0001c0001t0004g0256a0001c0001t0004g0262others(2): Show | 5 | HG00408.hp1 HG04184.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-3154_568-3149d others(8): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074590
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0002g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.568-3158_568-3149d others(12): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074590
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0002g0281 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.568-3160_568-3149d others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074590
|
CGT | C | 26 | a0001c0001t0001g0211a0001c0001t0001g0313a0001c0001t0001g0337others(23): Show | 26 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.568-3150_568-3149d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074590
|
CGTGT | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0094others(126): Show | 133 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.568-3152_568-3149d others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074590
|
CGTGTGT | C | 17 | a0001c0001t0001g0026a0001c0001t0001g0087a0001c0001t0001g0168others(14): Show | 17 | HG00597.hp1 HG00642.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.568-3154_568-3149d others(8): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074590
|
CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0001g0298a0001c0001t0003g0357a0001c0001t0005g0027others(3): Show | 6 | HG02280.hp2 HG02523.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-3156_568-3149d others(10): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074590
|
CGTGTGTG others(3): Show |
C | 1 | a0002c0002t0001g0187 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.568-3158_568-3149d others(12): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074590
|
CGTGTGTG others(5): Show |
C | 31 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0011g0322others(28): Show | 33 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.568-3160_568-3149d others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17074590 | |||||
| chr8:17074601
|
G | A | 1 | a0002c0002t0001g0187 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.568-3182G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074601 | ||||||
| chr8:17074603
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0011g0322others(28): Show | 33 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.568-3180G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074603 | ||||||
| chr8:17074892
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.568-2891G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074892 | ||||||
| chr8:17074929
|
T | G | 1 | a0001c0001t0003g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.568-2854T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074929 | ||||||
| chr8:17074983
|
T | C | 54 | a0001c0001t0001g0173a0001c0001t0002g0132a0001c0001t0002g0141others(51): Show | 55 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.568-2800T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17074983 | ||||||
| chr8:17075211
|
C | CA | 159 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.568-2571dupA | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17075211 | |||||
| chr8:17075350
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.568-2433T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17075350 | ||||||
| chr8:17075439
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.568-2344G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17075439 | ||||||
| chr8:17075549
|
G | GGA | 3 | a0001c0001t0001g0219a0001c0001t0018g0233a0001c0001t0018g0362 | 3 | HG02698.hp2 NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.568-2227_568-2226d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 17075549 | |||||
| chr8:17075631
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.568-2152T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17075631 | ||||||
| chr8:17075659
|
G | A | 106 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(103): Show | 107 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.568-2124G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17075659 | ||||||
| chr8:17075780
|
C | T | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.568-2003C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17075780 | ||||||
| chr8:17075795
|
T | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0013g0161 | 3 | HG00642.hp1 HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.568-1988T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17075795 | ||||||
| chr8:17075894
|
TAA | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0168a0001c0001t0001g0170others(22): Show | 27 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.568-1888_568-1887d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17075894 | ||||||
| chr8:17076047
|
G | A | 2 | a0001c0001t0002g0318a0001c0001t0015g0319 | 2 | NA18973.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.568-1736G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076047 | ||||||
| chr8:17076224
|
G | C | 1 | a0001c0003t0002g0202 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.568-1559G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076224 | ||||||
| chr8:17076338
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.568-1445A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076338 | ||||||
| chr8:17076353
|
C | A | 1 | a0001c0001t0006g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.568-1430C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076353 | ||||||
| chr8:17076418
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.568-1365T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076418 | ||||||
| chr8:17076425
|
C | T | 1 | a0001c0001t0002g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.568-1358C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076425 | ||||||
| chr8:17076442
|
G | A | 5 | a0001c0001t0002g0132a0001c0001t0002g0154a0001c0001t0002g0155others(2): Show | 5 | HG00544.hp2 HG02040.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-1341G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076442 | ||||||
| chr8:17076525
|
C | A | 359 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(356): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.568-1258C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076525 | ||||||
| chr8:17076855
|
C | T | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.568-928C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076855 | ||||||
| chr8:17076865
|
T | C | 106 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(103): Show | 108 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.568-918T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076865 | ||||||
| chr8:17076998
|
A | T | 2 | a0001c0001t0002g0252a0001c0001t0004g0265 | 2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.568-785A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17076998 | ||||||
| chr8:17077111
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.568-672A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17077111 | ||||||
| chr8:17077144
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.568-639C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17077144 | ||||||
| chr8:17077251
|
T | A | 105 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(102): Show | 107 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.568-532T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17077251 | ||||||
| chr8:17077461
|
A | G | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.568-322A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17077461 | ||||||
| chr8:17077462
|
T | A | 1 | a0001c0001t0001g0355 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.568-321T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17077462 | ||||||
| chr8:17077475
|
G | A | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.568-308G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17077475 | ||||||
| chr8:17077526
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.568-257C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17077526 | ||||||
| chr8:17077527
|
G | A | 1 | a0001c0001t0001g0355 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.568-256G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17077527 | ||||||
| chr8:17077725
|
G | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0167others(151): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.568-58G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 3/14 | chr8 | 17077725 | ||||||
| chr8:17077969
|
AT | A | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.646+109delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17077969 | ||||||
| chr8:17077971
|
G | A | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.646+110G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17077971 | ||||||
| chr8:17077972
|
C | T | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.646+111C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17077972 | ||||||
| chr8:17077973
|
A | T | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.646+112A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17077973 | ||||||
| chr8:17077986
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.646+125T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17077986 | ||||||
| chr8:17078015
|
T | G | 1 | a0001c0001t0002g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.646+154T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17078015 | ||||||
| chr8:17078066
|
T | A | 1 | a0002c0002t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.646+205T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17078066 | ||||||
| chr8:17078270
|
C | T | 16 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0128others(13): Show | 16 | HG00438.hp2 HG01433.hp2 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.646+409C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17078270 | ||||||
| chr8:17078450
|
T | C | 2 | a0001c0001t0014g0006a0001c0001t0014g0217 | 3 | HG02451.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.646+589T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17078450 | ||||||
| chr8:17078556
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.646+695G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17078556 | ||||||
| chr8:17078651
|
C | T | 178 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0074others(175): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.646+790C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17078651 | ||||||
| chr8:17078772
|
G | A | 78 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0294others(75): Show | 78 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.646+911G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17078772 | ||||||
| chr8:17078787
|
C | G | 1 | a0001c0001t0006g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.646+926C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17078787 | ||||||
| chr8:17079113
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.646+1252G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17079113 | ||||||
| chr8:17079143
|
CAT | C | 128 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(125): Show | 131 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.646+1283_646+1284d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17079143 | ||||||
| chr8:17079191
|
A | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.646+1330A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17079191 | ||||||
| chr8:17079195
|
C | T | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.646+1334C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17079195 | ||||||
| chr8:17079225
|
AT | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0074others(173): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.646+1365delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17079225 | ||||||
| chr8:17079343
|
G | A | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.646+1482G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17079343 | ||||||
| chr8:17079463
|
A | G | 2 | a0001c0001t0002g0127a0001c0001t0002g0129 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.646+1602A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17079463 | ||||||
| chr8:17079470
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.646+1609G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17079470 | ||||||
| chr8:17079858
|
G | A | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.647-1835G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17079858 | ||||||
| chr8:17079905
|
T | A | 2 | a0001c0001t0014g0006a0001c0001t0014g0217 | 3 | HG02451.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.647-1788T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17079905 | ||||||
| chr8:17080080
|
C | CT | 10 | a0001c0001t0002g0308a0001c0001t0002g0314a0001c0001t0002g0320others(7): Show | 10 | HG01891.hp2 HG02258.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.647-1603dupT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr8 | 17080080 | |||||
| chr8:17080231
|
A | G | 58 | a0001c0001t0001g0082a0001c0001t0001g0167a0001c0001t0002g0252others(55): Show | 60 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.647-1462A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17080231 | ||||||
| chr8:17080300
|
C | G | 3 | a0001c0001t0010g0022a0001c0001t0010g0023a0001c0001t0010g0227 | 3 | HG02280.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.647-1393C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17080300 | ||||||
| chr8:17080309
|
A | G | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 6 | HG01081.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.647-1384A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17080309 | ||||||
| chr8:17080462
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.647-1231C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17080462 | ||||||
| chr8:17080477
|
G | A | 78 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0294others(75): Show | 80 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.647-1216G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17080477 | ||||||
| chr8:17080532
|
G | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0074others(172): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.647-1161G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17080532 | ||||||
| chr8:17080561
|
T | C | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.647-1132T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17080561 | ||||||
| chr8:17080632
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.647-1061A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17080632 | ||||||
| chr8:17080687
|
T | C | 1 | a0001c0001t0004g0251 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.647-1006T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17080687 | ||||||
| chr8:17080804
|
C | T | 1 | a0003c0007t0002g0106 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.647-889C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17080804 | ||||||
| chr8:17081082
|
G | A | 1 | a0001c0001t0006g0028 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.647-611G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17081082 | ||||||
| chr8:17081161
|
T | C | 6 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0003t0007g0036others(3): Show | 6 | HG00642.hp1 HG00733.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.647-532T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17081161 | ||||||
| chr8:17081255
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.647-438T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17081255 | ||||||
| chr8:17081272
|
T | A | 8 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(5): Show | 8 | HG00642.hp1 HG00733.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.647-421T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17081272 | ||||||
| chr8:17081297
|
T | G | 8 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(5): Show | 8 | HG00642.hp1 HG00733.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.647-396T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17081297 | ||||||
| chr8:17081424
|
A | G | 9 | a0001c0001t0002g0275a0001c0001t0004g0255a0001c0001t0004g0259others(6): Show | 9 | HG00597.hp2 NA18940.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.647-269A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17081424 | ||||||
| chr8:17081439
|
C | G | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.647-254C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17081439 | ||||||
| chr8:17081549
|
C | A | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.647-144C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17081549 | ||||||
| chr8:17081557
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.647-136G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 4/14 | chr8 | 17081557 | ||||||
| chr8:17081775
|
G | A | 103 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(100): Show | 105 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.694+35G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17081775 | ||||||
| chr8:17081790
|
C | CA | 107 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(104): Show | 109 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.694+50_694+51insA | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17081790 | ||||||
| chr8:17081827
|
T | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.694+87T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17081827 | ||||||
| chr8:17081974
|
G | A | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.694+234G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17081974 | ||||||
| chr8:17081974
|
G | T | 1 | a0001c0001t0002g0132 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.694+234G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17081974 | ||||||
| chr8:17082150
|
A | AT | 57 | a0001c0001t0002g0132a0001c0001t0002g0141a0001c0001t0002g0154others(54): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.694+414dupT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 17082150 | |||||
| chr8:17082187
|
A | T | 1 | a0001c0001t0001g0323 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.694+447A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082187 | ||||||
| chr8:17082243
|
C | T | 2 | a0001c0001t0004g0247a0001c0001t0004g0250 | 2 | NA19001.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.694+503C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082243 | ||||||
| chr8:17082249
|
T | C | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.694+509T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082249 | ||||||
| chr8:17082283
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.694+543T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082283 | ||||||
| chr8:17082359
|
A | T | 55 | a0001c0001t0001g0082a0001c0001t0002g0252a0001c0001t0002g0275others(52): Show | 57 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.694+619A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082359 | ||||||
| chr8:17082369
|
T | A | 2 | a0001c0001t0004g0242a0001c0001t0004g0251 | 2 | HG02148.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.694+629T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082369 | ||||||
| chr8:17082602
|
G | A | 101 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(98): Show | 102 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.694+862G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082602 | ||||||
| chr8:17082639
|
A | G | 1 | a0001c0001t0001g0344 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.694+899A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082639 | ||||||
| chr8:17082763
|
G | A | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.694+1023G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082763 | ||||||
| chr8:17082793
|
T | C | 9 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.694+1053T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082793 | ||||||
| chr8:17082871
|
G | A | 101 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(98): Show | 102 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.694+1131G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082871 | ||||||
| chr8:17082911
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.694+1171A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17082911 | ||||||
| chr8:17083139
|
A | T | 1 | a0001c0001t0028g0302 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.694+1399A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083139 | ||||||
| chr8:17083225
|
C | T | 8 | a0002c0002t0001g0182a0002c0002t0001g0183a0002c0002t0001g0185others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.694+1485C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083225 | ||||||
| chr8:17083375
|
A | G | 2 | a0001c0001t0001g0297a0001c0001t0001g0311 | 2 | HG00621.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.694+1635A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083375 | ||||||
| chr8:17083451
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0168a0001c0001t0001g0170others(23): Show | 28 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.694+1711C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083451 | ||||||
| chr8:17083494
|
G | A | 15 | a0001c0001t0003g0069a0001c0001t0003g0072a0001c0001t0003g0076others(12): Show | 15 | HG01257.hp2 HG01496.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.695-1742G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083494 | ||||||
| chr8:17083776
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.695-1460G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083776 | ||||||
| chr8:17083823
|
A | C | 283 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(280): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.695-1413A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083823 | ||||||
| chr8:17083842
|
G | A | 174 | a0001c0001t0001g0007a0001c0001t0001g0074a0001c0001t0001g0082others(171): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.695-1394G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083842 | ||||||
| chr8:17083911
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.695-1325G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083911 | ||||||
| chr8:17083974
|
C | T | 1 | a0001c0004t0001g0209 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.695-1262C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083974 | ||||||
| chr8:17083990
|
G | A | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.695-1246G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083990 | ||||||
| chr8:17083991
|
G | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0011g0322others(29): Show | 34 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.695-1245G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17083991 | ||||||
| chr8:17084040
|
C | CA | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.695-1194dupA | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 17084040 | |||||
| chr8:17084155
|
C | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.695-1081C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17084155 | ||||||
| chr8:17084224
|
C | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.695-1012C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17084224 | ||||||
| chr8:17084228
|
T | C | 2 | a0001c0001t0006g0014a0001c0001t0025g0018 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.695-1008T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17084228 | ||||||
| chr8:17084252
|
T | G | 1 | a0001c0003t0002g0202 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.695-984T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17084252 | ||||||
| chr8:17084270
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.695-966C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17084270 | ||||||
| chr8:17084271
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.695-965G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17084271 | ||||||
| chr8:17084297
|
A | G | 1 | a0001c0001t0003g0100 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.695-939A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17084297 | ||||||
| chr8:17084453
|
TATC | T | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.695-782_695-780del others(3): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17084453 | ||||||
| chr8:17084537
|
C | T | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(99): Show | 103 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.695-699C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17084537 | ||||||
| chr8:17084841
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.695-395T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17084841 | ||||||
| chr8:17085102
|
A | G | 104 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(101): Show | 106 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.695-134A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 5/14 | chr8 | 17085102 | ||||||
| chr8:17085328
|
C | T | 283 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(280): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.777+10C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17085328 | ||||||
| chr8:17085334
|
G | C | 1 | a0001c0001t0006g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.777+16G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17085334 | ||||||
| chr8:17085340
|
C | T | 178 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0074others(175): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.777+22C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17085340 | ||||||
| chr8:17085385
|
G | A | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+67G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17085385 | ||||||
| chr8:17085628
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.777+310A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17085628 | ||||||
| chr8:17085906
|
T | A | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.777+588T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17085906 | ||||||
| chr8:17085993
|
A | G | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+675A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17085993 | ||||||
| chr8:17086005
|
A | G | 51 | a0001c0001t0002g0141a0001c0001t0003g0002a0001c0001t0003g0057others(48): Show | 52 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.777+687A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086005 | ||||||
| chr8:17086028
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.777+710T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086028 | ||||||
| chr8:17086063
|
C | A | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.777+745C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086063 | ||||||
| chr8:17086091
|
A | C | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.777+773A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086091 | ||||||
| chr8:17086146
|
C | T | 1 | a0001c0001t0003g0210 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.778-818C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086146 | ||||||
| chr8:17086203
|
C | T | 1 | a0001c0013t0021g0263 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.778-761C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086203 | ||||||
| chr8:17086280
|
T | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0168a0001c0001t0001g0170others(24): Show | 30 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.778-684T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086280 | ||||||
| chr8:17086317
|
A | G | 2 | a0001c0001t0006g0015a0001c0001t0006g0021 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.778-647A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086317 | ||||||
| chr8:17086326
|
C | T | 283 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(280): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.778-638C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086326 | ||||||
| chr8:17086387
|
C | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0011g0322others(26): Show | 31 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.778-577C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086387 | ||||||
| chr8:17086401
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.778-563G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086401 | ||||||
| chr8:17086655
|
G | A | 3 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-309G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086655 | ||||||
| chr8:17086896
|
C | T | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.778-68C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 6/14 | chr8 | 17086896 | ||||||
| chr8:17087100
|
G | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(38): Show | 44 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.849+65G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17087100 | ||||||
| chr8:17087263
|
T | C | 39 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(36): Show | 42 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.849+228T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17087263 | ||||||
| chr8:17087279
|
A | G | 1 | a0001c0001t0005g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.849+244A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17087279 | ||||||
| chr8:17087625
|
A | G | 58 | a0001c0001t0001g0300a0001c0001t0002g0141a0001c0001t0003g0002others(55): Show | 60 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.849+590A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17087625 | ||||||
| chr8:17087637
|
A | T | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.849+602A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17087637 | ||||||
| chr8:17087646
|
A | G | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+611A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17087646 | ||||||
| chr8:17087763
|
A | G | 1 | a0001c0001t0011g0322 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.849+728A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17087763 | ||||||
| chr8:17087951
|
T | A | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.849+916T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17087951 | ||||||
| chr8:17088070
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.849+1035G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088070 | ||||||
| chr8:17088148
|
A | G | 1 | a0001c0001t0002g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.849+1113A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088148 | ||||||
| chr8:17088289
|
C | T | 129 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0074others(126): Show | 136 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.849+1254C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088289 | ||||||
| chr8:17088296
|
G | C | 2 | a0001c0001t0014g0006a0001c0001t0014g0217 | 3 | HG02451.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.849+1261G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088296 | ||||||
| chr8:17088297
|
G | T | 1 | a0001c0003t0022g0055 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.849+1262G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088297 | ||||||
| chr8:17088326
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.849+1291C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088326 | ||||||
| chr8:17088369
|
C | A | 2 | a0001c0001t0018g0233a0001c0001t0018g0362 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.849+1334C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088369 | ||||||
| chr8:17088419
|
A | C | 1 | a0001c0001t0025g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849+1384A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088419 | ||||||
| chr8:17088482
|
T | G | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+1447T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088482 | ||||||
| chr8:17088563
|
A | C | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.849+1528A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088563 | ||||||
| chr8:17088640
|
G | A | 1 | a0001c0001t0008g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.849+1605G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088640 | ||||||
| chr8:17088746
|
G | A | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.849+1711G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088746 | ||||||
| chr8:17088749
|
A | C | 1 | a0001c0001t0001g0144 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.849+1714A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088749 | ||||||
| chr8:17088814
|
G | T | 1 | a0001c0001t0003g0062 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.850-1732G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088814 | ||||||
| chr8:17088824
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850-1722G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088824 | ||||||
| chr8:17088960
|
A | T | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.850-1586A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17088960 | ||||||
| chr8:17089101
|
A | G | 1 | a0001c0001t0002g0153 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.850-1445A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17089101 | ||||||
| chr8:17089297
|
T | A | 1 | a0001c0001t0002g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.850-1249T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17089297 | ||||||
| chr8:17089495
|
A | G | 1 | a0001c0001t0004g0157 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.850-1051A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17089495 | ||||||
| chr8:17089616
|
T | C | 36 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0236others(33): Show | 38 | HG01175.hp1 HG01243.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.850-930T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17089616 | ||||||
| chr8:17089675
|
C | T | 3 | a0001c0001t0002g0066a0001c0001t0002g0071a0001c0001t0002g0142 | 3 | HG00741.hp1 HG01358.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.850-871C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17089675 | ||||||
| chr8:17089751
|
A | G | 12 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0128others(9): Show | 12 | HG03654.hp2 HG03688.hp1 HG04199.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-795A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17089751 | ||||||
| chr8:17089786
|
A | G | 154 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(151): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.850-760A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17089786 | ||||||
| chr8:17090221
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.850-325A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17090221 | ||||||
| chr8:17090275
|
C | G | 83 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(80): Show | 87 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.850-271C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17090275 | ||||||
| chr8:17090391
|
C | T | 1 | a0001c0001t0003g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.850-155C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17090391 | ||||||
| chr8:17090464
|
G | A | 1 | a0001c0001t0028g0302 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.850-82G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 7/14 | chr8 | 17090464 | ||||||
| chr8:17090913
|
A | G | 1 | a0001c0001t0025g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.888+329A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17090913 | ||||||
| chr8:17090960
|
T | C | 106 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(103): Show | 107 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.888+376T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17090960 | ||||||
| chr8:17091130
|
T | A | 1 | a0001c0001t0001g0297 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.888+546T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091130 | ||||||
| chr8:17091145
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.888+561A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091145 | ||||||
| chr8:17091278
|
C | G | 3 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.888+694C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091278 | ||||||
| chr8:17091291
|
G | A | 101 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(98): Show | 102 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.888+707G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091291 | ||||||
| chr8:17091382
|
T | C | 2 | a0001c0001t0002g0050a0001c0001t0002g0073 | 2 | HG00280.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.888+798T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091382 | ||||||
| chr8:17091518
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.888+934T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091518 | ||||||
| chr8:17091583
|
C | T | 55 | a0001c0001t0001g0082a0001c0001t0002g0252a0001c0001t0002g0275others(52): Show | 57 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.888+999C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091583 | ||||||
| chr8:17091596
|
A | G | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.888+1012A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091596 | ||||||
| chr8:17091683
|
C | T | 1 | a0001c0001t0006g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.888+1099C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091683 | ||||||
| chr8:17091732
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.888+1148T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091732 | ||||||
| chr8:17091833
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.888+1249A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091833 | ||||||
| chr8:17091870
|
G | T | 3 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.888+1286G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091870 | ||||||
| chr8:17091871
|
T | G | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.888+1287T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091871 | ||||||
| chr8:17091876
|
T | G | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.888+1292T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091876 | ||||||
| chr8:17091918
|
G | A | 2 | a0002c0002t0005g0186a0002c0002t0005g0190 | 2 | HG01361.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.888+1334G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091918 | ||||||
| chr8:17091965
|
A | G | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.888+1381A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091965 | ||||||
| chr8:17091992
|
C | T | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.888+1408C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17091992 | ||||||
| chr8:17092153
|
C | G | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.888+1569C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092153 | ||||||
| chr8:17092155
|
C | T | 1 | a0001c0001t0003g0295 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.888+1571C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092155 | ||||||
| chr8:17092209
|
C | T | 196 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(193): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.888+1625C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092209 | ||||||
| chr8:17092315
|
C | T | 1 | a0001c0001t0002g0287 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.888+1731C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092315 | ||||||
| chr8:17092356
|
C | G | 82 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(79): Show | 85 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.888+1772C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092356 | ||||||
| chr8:17092366
|
C | T | 1 | a0001c0001t0004g0245 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.888+1782C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092366 | ||||||
| chr8:17092612
|
CTA | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0220 | 3 | NA18951.hp2 NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.888+2030_888+2031d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17092612 | |||||
| chr8:17092804
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.888+2220G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092804 | ||||||
| chr8:17092889
|
G | A | 1 | a0001c0001t0003g0149 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.888+2305G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092889 | ||||||
| chr8:17092890
|
G | A | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.888+2306G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092890 | ||||||
| chr8:17092892
|
T | C | 2 | a0001c0001t0002g0360a0001c0001t0002g0361 | 2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.888+2308T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092892 | ||||||
| chr8:17092914
|
A | G | 1 | a0001c0001t0011g0322 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.888+2330A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17092914 | ||||||
| chr8:17093137
|
T | A | 1 | a0002c0002t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.888+2553T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17093137 | ||||||
| chr8:17093190
|
T | C | 1 | a0001c0001t0004g0068 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.888+2606T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17093190 | ||||||
| chr8:17093233
|
C | T | 1 | a0001c0001t0004g0260 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.888+2649C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17093233 | ||||||
| chr8:17093361
|
A | G | 3 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.888+2777A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17093361 | ||||||
| chr8:17093452
|
G | A | 1 | a0001c0001t0003g0283 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.888+2868G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17093452 | ||||||
| chr8:17093752
|
ATC | A | 2 | a0001c0001t0014g0006a0001c0001t0014g0217 | 3 | HG02451.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.888+3172_888+3173d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17093752 | |||||
| chr8:17093773
|
G | A | 290 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(287): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.888+3189G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17093773 | ||||||
| chr8:17093805
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0205others(31): Show | 36 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.888+3221G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17093805 | ||||||
| chr8:17093919
|
A | G | 30 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0051others(27): Show | 30 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.888+3335A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17093919 | ||||||
| chr8:17093934
|
C | A | 1 | a0001c0001t0012g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.888+3350C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17093934 | ||||||
| chr8:17093989
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.888+3405A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17093989 | ||||||
| chr8:17094016
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.888+3432A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094016 | ||||||
| chr8:17094046
|
CT | C | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.888+3466delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17094046 | |||||
| chr8:17094069
|
C | T | 101 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(98): Show | 101 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.888+3485C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094069 | ||||||
| chr8:17094286
|
C | G | 1 | a0001c0003t0020g0053 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.888+3702C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094286 | ||||||
| chr8:17094295
|
T | C | 102 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(99): Show | 103 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.888+3711T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094295 | ||||||
| chr8:17094326
|
T | C | 1 | a0001c0001t0002g0304 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.888+3742T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094326 | ||||||
| chr8:17094417
|
C | G | 1 | a0001c0001t0001g0121 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.888+3833C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094417 | ||||||
| chr8:17094477
|
G | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.888+3893G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094477 | ||||||
| chr8:17094505
|
A | G | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.888+3921A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094505 | ||||||
| chr8:17094547
|
G | A | 289 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(286): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.889-3911G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094547 | ||||||
| chr8:17094666
|
G | A | 1 | a0004c0010t0002g0280 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.889-3792G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094666 | ||||||
| chr8:17094686
|
A | G | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-3772A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094686 | ||||||
| chr8:17094911
|
C | T | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.889-3547C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094911 | ||||||
| chr8:17094912
|
G | A | 3 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0232 | 3 | HG03490.hp2 HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.889-3546G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094912 | ||||||
| chr8:17094912
|
G | C | 2 | a0001c0001t0002g0252a0001c0001t0004g0265 | 2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.889-3546G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17094912 | ||||||
| chr8:17095012
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(1): Show | 4 | HG00642.hp1 HG00733.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-3446C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17095012 | ||||||
| chr8:17095241
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.889-3217T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17095241 | ||||||
| chr8:17095292
|
T | G | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.889-3166T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17095292 | ||||||
| chr8:17095451
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.889-3007G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17095451 | ||||||
| chr8:17095462
|
A | T | 49 | a0001c0001t0003g0002a0001c0001t0003g0057a0001c0001t0003g0059others(46): Show | 51 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.889-2996A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17095462 | ||||||
| chr8:17095529
|
A | G | 56 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(53): Show | 57 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.889-2929A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17095529 | ||||||
| chr8:17095539
|
A | G | 4 | a0001c0001t0004g0255a0001c0001t0004g0259a0001c0001t0004g0260others(1): Show | 4 | HG00597.hp2 NA18940.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-2919A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17095539 | ||||||
| chr8:17095619
|
T | C | 1 | a0002c0002t0017g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.889-2839T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17095619 | ||||||
| chr8:17096047
|
T | G | 1 | a0001c0001t0001g0354 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.889-2411T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096047 | ||||||
| chr8:17096103
|
C | G | 3 | a0001c0001t0010g0022a0001c0001t0010g0023a0001c0001t0010g0227 | 3 | HG02280.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.889-2355C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096103 | ||||||
| chr8:17096148
|
C | T | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.889-2310C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096148 | ||||||
| chr8:17096165
|
T | C | 104 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0121others(101): Show | 105 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.889-2293T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096165 | ||||||
| chr8:17096233
|
T | C | 4 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285others(1): Show | 4 | HG02818.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-2225T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096233 | ||||||
| chr8:17096298
|
C | G | 3 | a0001c0001t0010g0022a0001c0001t0010g0023a0001c0001t0010g0227 | 3 | HG02280.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.889-2160C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096298 | ||||||
| chr8:17096440
|
C | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0236others(33): Show | 38 | HG01175.hp1 HG01243.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.889-2018C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096440 | ||||||
| chr8:17096651
|
G | C | 2 | a0003c0007t0002g0064a0003c0007t0002g0106 | 2 | HG01934.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.889-1807G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096651 | ||||||
| chr8:17096661
|
C | T | 1 | a0002c0002t0001g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.889-1797C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096661 | ||||||
| chr8:17096759
|
T | C | 96 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(93): Show | 101 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.889-1699T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096759 | ||||||
| chr8:17096909
|
A | T | 1 | a0001c0001t0011g0322 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.889-1549A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096909 | ||||||
| chr8:17096922
|
C | T | 1 | a0002c0002t0001g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.889-1536C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096922 | ||||||
| chr8:17096934
|
C | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.889-1524C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17096934 | ||||||
| chr8:17096955
|
T | TTG | 12 | a0001c0001t0001g0040a0001c0001t0001g0170a0001c0001t0001g0173others(9): Show | 12 | HG00558.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.889-1462_889-1461d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17096955
|
T | TTGTG | 56 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(53): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.889-1464_889-1461d others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17096955
|
T | TTGTGTG | 6 | a0001c0001t0001g0221a0001c0001t0001g0228a0001c0001t0003g0069others(3): Show | 6 | HG00738.hp1 HG02004.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.889-1466_889-1461d others(8): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17096955
|
T | TTGTGTGT others(1): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0223a0001c0001t0003g0091others(2): Show | 6 | HG02976.hp1 HG06807.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-1468_889-1461d others(10): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17096955
|
T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0065a0001c0001t0001g0220a0001c0001t0005g0226 | 3 | HG02145.hp1 HG02300.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.889-1470_889-1461d others(12): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17096955
|
TTG | T | 70 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0049others(67): Show | 72 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.889-1462_889-1461d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17096955
|
TTGTG | T | 12 | a0001c0001t0001g0359a0001c0001t0002g0159a0001c0001t0002g0360others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.889-1464_889-1461d others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17096955
|
TTGTGTGT others(1): Show |
T | 24 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0167others(21): Show | 24 | HG00735.hp1 HG01109.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.889-1468_889-1461d others(10): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17096955
|
TTGTGTGT others(3): Show |
T | 54 | a0001c0001t0001g0082a0001c0001t0001g0323a0001c0001t0001g0352others(51): Show | 56 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.889-1470_889-1461d others(12): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17096955
|
TTGTGTGT others(5): Show |
T | 79 | a0001c0001t0001g0121a0001c0001t0001g0144a0001c0001t0001g0293others(76): Show | 80 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.889-1472_889-1461d others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17096955
|
TTGTGTGT others(7): Show |
T | 6 | a0001c0001t0002g0252a0001c0001t0003g0283a0001c0001t0004g0257others(3): Show | 6 | HG02155.hp1 HG02818.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-1474_889-1461d others(16): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17096955 | |||||
| chr8:17097163
|
C | T | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.889-1295C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097163 | ||||||
| chr8:17097210
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.889-1248T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097210 | ||||||
| chr8:17097253
|
A | G | 1 | a0001c0001t0003g0092 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.889-1205A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097253 | ||||||
| chr8:17097267
|
T | C | 1 | a0001c0001t0006g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.889-1191T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097267 | ||||||
| chr8:17097331
|
T | C | 363 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(360): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.889-1127T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097331 | ||||||
| chr8:17097399
|
CTG | C | 6 | a0001c0001t0002g0308a0001c0001t0002g0314a0001c0001t0002g0320others(3): Show | 6 | HG02735.hp2 HG03927.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-1055_889-1054d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr8 | 17097399 | |||||
| chr8:17097531
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.889-927T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097531 | ||||||
| chr8:17097537
|
G | C | 1 | a0002c0002t0001g0364 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.889-921G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097537 | ||||||
| chr8:17097700
|
A | G | 1 | a0001c0001t0002g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.889-758A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097700 | ||||||
| chr8:17097766
|
C | T | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.889-692C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097766 | ||||||
| chr8:17097786
|
A | C | 4 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285others(1): Show | 4 | HG02818.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-672A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097786 | ||||||
| chr8:17097824
|
A | C | 1 | a0001c0001t0010g0023 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.889-634A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097824 | ||||||
| chr8:17097882
|
C | T | 4 | a0001c0001t0003g0215a0001c0001t0003g0288a0001c0001t0003g0291others(1): Show | 4 | HG00099.hp2 HG01255.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-576C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097882 | ||||||
| chr8:17097919
|
A | G | 48 | a0001c0001t0003g0002a0001c0001t0003g0057a0001c0001t0003g0059others(45): Show | 49 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.889-539A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17097919 | ||||||
| chr8:17098004
|
T | C | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-454T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17098004 | ||||||
| chr8:17098096
|
A | C | 1 | a0006c0008t0026g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.889-362A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17098096 | ||||||
| chr8:17098173
|
G | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(15): Show | 18 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.889-285G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17098173 | ||||||
| chr8:17098189
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0013g0161 | 3 | HG00642.hp1 HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.889-269A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17098189 | ||||||
| chr8:17098242
|
C | G | 74 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(71): Show | 76 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.889-216C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17098242 | ||||||
| chr8:17098327
|
CAAAA | C | 71 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(68): Show | 72 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.889-130_889-127del others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17098327 | ||||||
| chr8:17098328
|
A | C | 1 | a0001c0001t0006g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.889-130A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 8/14 | chr8 | 17098328 | ||||||
| chr8:17098584
|
C | G | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.984+31C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17098584 | ||||||
| chr8:17098752
|
C | A | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.984+199C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17098752 | ||||||
| chr8:17099116
|
G | A | 3 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0115 | 3 | HG03098.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.984+563G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17099116 | ||||||
| chr8:17099161
|
A | G | 80 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(77): Show | 82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.984+608A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17099161 | ||||||
| chr8:17099228
|
C | G | 35 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(32): Show | 38 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.984+675C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17099228 | ||||||
| chr8:17099410
|
A | C | 26 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(23): Show | 26 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.984+857A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17099410 | ||||||
| chr8:17099472
|
T | C | 1 | a0001c0001t0002g0290 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.984+919T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17099472 | ||||||
| chr8:17099665
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.984+1112T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17099665 | ||||||
| chr8:17099865
|
C | G | 1 | a0001c0001t0002g0318 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.984+1312C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17099865 | ||||||
| chr8:17099991
|
C | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(37): Show | 43 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.984+1438C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17099991 | ||||||
| chr8:17100177
|
A | G | 4 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285others(1): Show | 4 | HG02818.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.984+1624A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100177 | ||||||
| chr8:17100224
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0040others(78): Show | 86 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.984+1671C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100224 | ||||||
| chr8:17100247
|
A | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.984+1694A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100247 | ||||||
| chr8:17100392
|
G | A | 72 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(69): Show | 73 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.984+1839G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100392 | ||||||
| chr8:17100481
|
T | C | 1 | a0001c0001t0002g0329 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.984+1928T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100481 | ||||||
| chr8:17100496
|
T | C | 1 | a0001c0001t0002g0360 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.984+1943T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100496 | ||||||
| chr8:17100560
|
T | C | 1 | a0001c0001t0003g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.984+2007T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100560 | ||||||
| chr8:17100623
|
A | G | 1 | a0001c0001t0004g0251 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.984+2070A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100623 | ||||||
| chr8:17100690
|
C | A | 1 | a0001c0001t0001g0326 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.984+2137C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100690 | ||||||
| chr8:17100750
|
C | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(211): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.984+2197C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100750 | ||||||
| chr8:17100775
|
G | T | 2 | a0001c0001t0003g0135a0001c0001t0016g0088 | 2 | NA18979.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.984+2222G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17100775 | ||||||
| chr8:17101001
|
T | G | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.984+2448T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17101001 | ||||||
| chr8:17101040
|
G | A | 1 | a0001c0001t0001g0354 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.984+2487G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17101040 | ||||||
| chr8:17101202
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0142 | 2 | HG01358.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.984+2649A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17101202 | ||||||
| chr8:17101311
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.984+2758T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17101311 | ||||||
| chr8:17101556
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.985-2835T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17101556 | ||||||
| chr8:17101758
|
T | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.985-2633T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17101758 | ||||||
| chr8:17102122
|
C | CTATTTG | 6 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0268others(3): Show | 6 | NA18954.hp2 NA18964.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-2268_985-2267i others(8): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 17102122 | |||||
| chr8:17102169
|
C | G | 5 | a0001c0001t0001g0070a0001c0001t0001g0168a0001c0001t0001g0170others(2): Show | 5 | HG00642.hp2 HG01081.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-2222C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102169 | ||||||
| chr8:17102261
|
A | G | 1 | a0002c0002t0001g0364 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.985-2130A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102261 | ||||||
| chr8:17102301
|
G | A | 1 | a0002c0002t0001g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.985-2090G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102301 | ||||||
| chr8:17102456
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.985-1935C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102456 | ||||||
| chr8:17102513
|
GT | G | 206 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(203): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.985-1876delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 17102513 | |||||
| chr8:17102515
|
T | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.985-1876T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102515 | ||||||
| chr8:17102522
|
A | G | 1 | a0001c0001t0003g0230 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.985-1869A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102522 | ||||||
| chr8:17102581
|
C | T | 5 | a0001c0001t0001g0070a0001c0001t0001g0168a0001c0001t0001g0170others(2): Show | 5 | HG00642.hp2 HG01081.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-1810C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102581 | ||||||
| chr8:17102597
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.985-1794G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102597 | ||||||
| chr8:17102673
|
A | G | 4 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.985-1718A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102673 | ||||||
| chr8:17102809
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.985-1582G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102809 | ||||||
| chr8:17102811
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.985-1580T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17102811 | ||||||
| chr8:17103004
|
T | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.985-1387T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17103004 | ||||||
| chr8:17103032
|
C | T | 46 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(43): Show | 49 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.985-1359C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17103032 | ||||||
| chr8:17103305
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.985-1086G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17103305 | ||||||
| chr8:17103380
|
C | G | 3 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0016g0088 | 3 | NA18969.hp1 NA18979.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.985-1011C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17103380 | ||||||
| chr8:17103531
|
T | C | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.985-860T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17103531 | ||||||
| chr8:17103576
|
A | AGAAG | 58 | a0001c0001t0001g0082a0001c0001t0001g0167a0001c0001t0002g0252others(55): Show | 60 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-793_985-790dup others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 17103576 | |||||
| chr8:17103576
|
AGAAG | A | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.985-793_985-790del others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 17103576 | |||||
| chr8:17103774
|
C | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0008g0011others(30): Show | 35 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.985-617C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17103774 | ||||||
| chr8:17103781
|
C | T | 212 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(209): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.985-610C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17103781 | ||||||
| chr8:17103911
|
G | T | 3 | a0001c0001t0001g0236a0001c0001t0005g0234a0001c0001t0005g0235 | 3 | HG01243.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.985-480G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17103911 | ||||||
| chr8:17103968
|
G | A | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.985-423G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17103968 | ||||||
| chr8:17104097
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.985-294A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17104097 | ||||||
| chr8:17104199
|
T | C | 39 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(36): Show | 42 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.985-192T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17104199 | ||||||
| chr8:17104345
|
G | T | 1 | a0001c0001t0004g0250 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.985-46G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 9/14 | chr8 | 17104345 | ||||||
| chr8:17104514
|
A | G | 3 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356 | 3 | HG02258.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1085+23A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | chr8 | 17104514 | ||||||
| chr8:17104630
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1085+139A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | chr8 | 17104630 | ||||||
| chr8:17104677
|
A | G | 3 | a0001c0001t0005g0218a0001c0001t0005g0225a0001c0001t0005g0226 | 3 | HG02145.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1085+186A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | chr8 | 17104677 | ||||||
| chr8:17104696
|
TTAAAAAT others(315): Show |
T | 5 | a0001c0001t0004g0257a0001c0001t0004g0268a0001c0001t0004g0273others(2): Show | 5 | HG02155.hp1 NA18964.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085+206_1086-395d others(2): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | chr8 | 17104696 | ||||||
| chr8:17104697
|
TAAAAATT others(315): Show |
T | 208 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(205): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1085+223_1086-378d others(2): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 17104697 | |||||
| chr8:17104819
|
C | A | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1085+328C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | chr8 | 17104819 | ||||||
| chr8:17104994
|
C | CA | 55 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0058others(52): Show | 55 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1086-389dupA | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 17104994 | |||||
| chr8:17104994
|
C | CAA | 10 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0315others(7): Show | 10 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.1086-390_1086-389d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 17104994 | |||||
| chr8:17104994
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1086-401_1086-389d others(15): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 17104994 | |||||
| chr8:17105051
|
C | T | 1 | a0001c0001t0004g0256 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1086-362C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | chr8 | 17105051 | ||||||
| chr8:17105172
|
T | C | 2 | a0002c0002t0017g0188a0002c0002t0017g0194 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1086-241T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | chr8 | 17105172 | ||||||
| chr8:17105253
|
T | C | 134 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(131): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1086-160T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | chr8 | 17105253 | ||||||
| chr8:17105277
|
A | T | 2 | a0001c0001t0014g0006a0001c0001t0014g0217 | 3 | HG02451.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1086-136A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/14 | chr8 | 17105277 | ||||||
| chr8:17105677
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1257+93T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17105677 | ||||||
| chr8:17105813
|
A | G | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257+229A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17105813 | ||||||
| chr8:17105820
|
A | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(30): Show | 35 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1257+236A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17105820 | ||||||
| chr8:17105853
|
A | T | 76 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(73): Show | 78 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1257+269A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17105853 | ||||||
| chr8:17105866
|
T | C | 1 | a0001c0001t0006g0014 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1257+282T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17105866 | ||||||
| chr8:17106037
|
A | C | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1257+453A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106037 | ||||||
| chr8:17106174
|
A | G | 5 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285others(2): Show | 6 | HG02451.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1257+590A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106174 | ||||||
| chr8:17106200
|
A | C | 214 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(211): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1257+616A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106200 | ||||||
| chr8:17106329
|
C | A | 5 | a0001c0001t0001g0070a0001c0001t0001g0168a0001c0001t0001g0170others(2): Show | 5 | HG00642.hp2 HG01081.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257+745C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106329 | ||||||
| chr8:17106348
|
A | G | 38 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(35): Show | 40 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1257+764A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106348 | ||||||
| chr8:17106434
|
C | T | 1 | a0001c0003t0020g0053 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1257+850C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106434 | ||||||
| chr8:17106438
|
A | C | 1 | a0001c0001t0003g0057 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1257+854A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106438 | ||||||
| chr8:17106450
|
C | A | 47 | a0001c0001t0003g0002a0001c0001t0003g0057a0001c0001t0003g0059others(44): Show | 48 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.1257+866C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106450 | ||||||
| chr8:17106546
|
CT | C | 56 | a0001c0001t0001g0082a0001c0001t0001g0167a0001c0001t0002g0252others(53): Show | 58 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1257+978delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 17106546 | |||||
| chr8:17106546
|
CTT | C | 70 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0026others(67): Show | 73 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(70): Show |
intron_variant | MODIFIER | c.1257+977_1257+978d others(4): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 17106546 | |||||
| chr8:17106546
|
CTTT | C | 83 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(80): Show | 86 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1257+976_1257+978d others(5): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 17106546 | |||||
| chr8:17106554
|
T | A | 81 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0294others(78): Show | 82 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1257+970T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106554 | ||||||
| chr8:17106691
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1257+1107T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106691 | ||||||
| chr8:17106788
|
CTTTCTTC others(7): Show |
C | 19 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(16): Show | 19 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1257+1208_1257+122 others(18): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 17106788 | |||||
| chr8:17106842
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1257+1258C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106842 | ||||||
| chr8:17106843
|
G | A | 1 | a0001c0001t0002g0358 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1257+1259G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106843 | ||||||
| chr8:17106900
|
T | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0008g0011others(31): Show | 36 | HG01175.hp1 HG01361.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.1257+1316T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106900 | ||||||
| chr8:17106916
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1257+1332C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17106916 | ||||||
| chr8:17107058
|
T | C | 57 | a0001c0001t0001g0082a0001c0001t0001g0167a0001c0001t0002g0252others(54): Show | 59 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1257+1474T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17107058 | ||||||
| chr8:17107522
|
G | C | 2 | a0001c0001t0003g0124a0001c0001t0003g0152 | 2 | HG01257.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1257+1938G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17107522 | ||||||
| chr8:17107522
|
G | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0236others(33): Show | 38 | HG01175.hp1 HG01243.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.1257+1938G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17107522 | ||||||
| chr8:17107567
|
G | T | 127 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(124): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1257+1983G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17107567 | ||||||
| chr8:17107783
|
C | A | 1 | a0001c0001t0001g0103 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1257+2199C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17107783 | ||||||
| chr8:17108065
|
G | A | 1 | a0001c0009t0001g0019 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1257+2481G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17108065 | ||||||
| chr8:17108278
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1257+2694A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17108278 | ||||||
| chr8:17108459
|
A | G | 1 | a0001c0001t0028g0302 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1257+2875A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17108459 | ||||||
| chr8:17108468
|
C | A | 169 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0026others(166): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1257+2884C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17108468 | ||||||
| chr8:17108546
|
G | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0236others(33): Show | 38 | HG01175.hp1 HG01243.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.1257+2962G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17108546 | ||||||
| chr8:17108552
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1257+2968C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17108552 | ||||||
| chr8:17108587
|
G | C | 127 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(124): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1257+3003G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17108587 | ||||||
| chr8:17108625
|
C | T | 123 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(120): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1257+3041C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17108625 | ||||||
| chr8:17108713
|
C | A | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1257+3129C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17108713 | ||||||
| chr8:17109034
|
A | G | 7 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0013g0161others(4): Show | 7 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1257+3450A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17109034 | ||||||
| chr8:17109036
|
G | T | 122 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(119): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1257+3452G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17109036 | ||||||
| chr8:17109225
|
T | C | 26 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(23): Show | 26 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1257+3641T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17109225 | ||||||
| chr8:17109695
|
A | G | 1 | a0001c0001t0003g0357 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1257+4111A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17109695 | ||||||
| chr8:17109760
|
A | C | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1257+4176A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17109760 | ||||||
| chr8:17109883
|
G | A | 47 | a0001c0001t0003g0002a0001c0001t0003g0057a0001c0001t0003g0059others(44): Show | 48 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.1258-4210G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17109883 | ||||||
| chr8:17109905
|
G | T | 1 | a0003c0007t0002g0064 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1258-4188G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17109905 | ||||||
| chr8:17109983
|
C | A | 1 | a0001c0001t0003g0210 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1258-4110C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17109983 | ||||||
| chr8:17110042
|
C | G | 3 | a0001c0001t0010g0022a0001c0001t0010g0023a0001c0001t0010g0227 | 3 | HG02280.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1258-4051C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110042 | ||||||
| chr8:17110075
|
A | C | 213 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(210): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1258-4018A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110075 | ||||||
| chr8:17110216
|
G | C | 57 | a0001c0001t0001g0082a0001c0001t0001g0167a0001c0001t0002g0252others(54): Show | 59 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1258-3877G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110216 | ||||||
| chr8:17110290
|
G | A | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1258-3803G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110290 | ||||||
| chr8:17110462
|
C | A | 73 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(70): Show | 75 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1258-3631C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110462 | ||||||
| chr8:17110618
|
C | G | 2 | a0001c0001t0002g0360a0001c0001t0002g0361 | 2 | HG03654.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1258-3475C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110618 | ||||||
| chr8:17110642
|
T | C | 295 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(292): Show | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1258-3451T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110642 | ||||||
| chr8:17110648
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(1): Show | 4 | HG00642.hp1 HG00733.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258-3445C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110648 | ||||||
| chr8:17110736
|
T | G | 1 | a0002c0002t0001g0179 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1258-3357T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110736 | ||||||
| chr8:17110741
|
A | AG | 91 | a0001c0001t0001g0121a0001c0001t0001g0144a0001c0001t0001g0293others(88): Show | 93 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1258-3344dupG | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 17110741 | |||||
| chr8:17110823
|
C | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1258-3270C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110823 | ||||||
| chr8:17110869
|
A | T | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1258-3224A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110869 | ||||||
| chr8:17110885
|
T | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0205a0002c0002t0001g0191others(4): Show | 8 | HG02257.hp2 HG02809.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1258-3208T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17110885 | ||||||
| chr8:17111071
|
T | C | 3 | a0001c0001t0003g0283a0001c0001t0003g0284a0001c0001t0003g0285 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1258-3022T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111071 | ||||||
| chr8:17111132
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1258-2961G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111132 | ||||||
| chr8:17111144
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1258-2949G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111144 | ||||||
| chr8:17111326
|
T | G | 5 | a0001c0001t0008g0011a0002c0002t0001g0178a0002c0002t0008g0172others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-2767T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111326 | ||||||
| chr8:17111364
|
C | G | 1 | a0001c0001t0002g0345 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1258-2729C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111364 | ||||||
| chr8:17111392
|
A | G | 1 | a0001c0001t0003g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1258-2701A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111392 | ||||||
| chr8:17111423
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1258-2670G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111423 | ||||||
| chr8:17111423
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1258-2670G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111423 | ||||||
| chr8:17111487
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0205 | 3 | HG02809.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1258-2606A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111487 | ||||||
| chr8:17111789
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1258-2304A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111789 | ||||||
| chr8:17111820
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1258-2273C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111820 | ||||||
| chr8:17111921
|
A | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1258-2172A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17111921 | ||||||
| chr8:17112013
|
G | A | 294 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(291): Show | 303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1258-2080G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112013 | ||||||
| chr8:17112058
|
A | G | 163 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(160): Show | 166 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1258-2035A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112058 | ||||||
| chr8:17112059
|
TG | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0236others(35): Show | 40 | HG01175.hp1 HG01243.hp1 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.1258-2030delG | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 17112059 | |||||
| chr8:17112161
|
G | T | 5 | a0001c0001t0001g0070a0001c0001t0001g0168a0001c0001t0001g0170others(2): Show | 5 | HG00642.hp2 HG01081.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-1932G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112161 | ||||||
| chr8:17112256
|
A | G | 57 | a0001c0001t0001g0082a0001c0001t0001g0167a0001c0001t0002g0252others(54): Show | 59 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1258-1837A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112256 | ||||||
| chr8:17112312
|
G | T | 208 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0082others(205): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1258-1781G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112312 | ||||||
| chr8:17112384
|
A | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0359a0001c0001t0002g0360others(2): Show | 5 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1258-1709A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112384 | ||||||
| chr8:17112399
|
T | G | 294 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(291): Show | 303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1258-1694T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112399 | ||||||
| chr8:17112421
|
A | G | 5 | a0001c0001t0001g0048a0001c0001t0002g0001a0001c0001t0002g0162others(2): Show | 6 | HG00639.hp1 HG01109.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1258-1672A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112421 | ||||||
| chr8:17112448
|
T | A | 48 | a0001c0001t0003g0002a0001c0001t0003g0057a0001c0001t0003g0059others(45): Show | 49 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.1258-1645T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112448 | ||||||
| chr8:17112516
|
C | T | 1 | a0001c0001t0002g0349 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1258-1577C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112516 | ||||||
| chr8:17112517
|
C | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0236others(35): Show | 40 | HG01175.hp1 HG01243.hp1 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.1258-1576C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112517 | ||||||
| chr8:17112676
|
A | T | 1 | a0001c0001t0002g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1258-1417A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112676 | ||||||
| chr8:17112769
|
C | T | 1 | a0001c0001t0002g0287 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1258-1324C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112769 | ||||||
| chr8:17112773
|
C | T | 56 | a0001c0001t0001g0082a0001c0001t0001g0167a0001c0001t0002g0252others(53): Show | 58 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1258-1320C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112773 | ||||||
| chr8:17112781
|
A | T | 35 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(32): Show | 38 | HG00642.hp2 HG00738.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1258-1312A>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112781 | ||||||
| chr8:17112783
|
C | G | 56 | a0001c0001t0001g0082a0001c0001t0001g0167a0001c0001t0002g0252others(53): Show | 58 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1258-1310C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112783 | ||||||
| chr8:17112816
|
G | A | 1 | a0001c0001t0002g0363 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1258-1277G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112816 | ||||||
| chr8:17112845
|
G | A | 83 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0294others(80): Show | 84 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1258-1248G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112845 | ||||||
| chr8:17112936
|
A | G | 1 | a0001c0003t0002g0200 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1258-1157A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17112936 | ||||||
| chr8:17113014
|
G | A | 1 | a0001c0001t0010g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1258-1079G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17113014 | ||||||
| chr8:17113402
|
C | G | 1 | a0001c0001t0001g0356 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1258-691C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17113402 | ||||||
| chr8:17113748
|
C | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0037others(126): Show | 135 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.1258-345C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17113748 | ||||||
| chr8:17113759
|
T | TA | 16 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1258-326dupA | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 17113759 | |||||
| chr8:17113807
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1258-286T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17113807 | ||||||
| chr8:17113828
|
T | G | 1 | a0001c0001t0002g0042 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1258-265T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17113828 | ||||||
| chr8:17113881
|
A | G | 208 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0037others(205): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1258-212A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17113881 | ||||||
| chr8:17113949
|
GAAC | G | 15 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1258-140_1258-138d others(5): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 17113949 | |||||
| chr8:17113955
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1258-138C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17113955 | ||||||
| chr8:17114057
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0232 | 2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1258-36A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17114057 | ||||||
| chr8:17114060
|
C | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1258-33C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 11/14 | chr8 | 17114060 | ||||||
| chr8:17114255
|
A | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1366+54A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114255 | ||||||
| chr8:17114275
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1366+74A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114275 | ||||||
| chr8:17114425
|
G | A | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1366+224G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114425 | ||||||
| chr8:17114442
|
G | A | 15 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366+241G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114442 | ||||||
| chr8:17114462
|
G | A | 54 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0068others(51): Show | 56 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1366+261G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114462 | ||||||
| chr8:17114704
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1366+503T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114704 | ||||||
| chr8:17114748
|
C | G | 1 | a0001c0001t0001g0298 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1366+547C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114748 | ||||||
| chr8:17114753
|
C | A | 1 | a0001c0003t0002g0202 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1366+552C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114753 | ||||||
| chr8:17114754
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG02965.hp1 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1366+553C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114754 | ||||||
| chr8:17114822
|
C | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1366+621C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114822 | ||||||
| chr8:17114841
|
C | T | 5 | a0001c0001t0001g0300a0001c0001t0001g0315a0001c0001t0001g0316others(2): Show | 5 | HG01346.hp2 HG01433.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366+640C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114841 | ||||||
| chr8:17114858
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0002g0330 | 2 | HG00609.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1366+657G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114858 | ||||||
| chr8:17114890
|
C | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1366+689C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114890 | ||||||
| chr8:17114890
|
C | T | 3 | a0002c0002t0001g0197a0002c0002t0017g0188a0002c0002t0017g0194 | 3 | HG02886.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1366+689C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114890 | ||||||
| chr8:17114987
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1366+786C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17114987 | ||||||
| chr8:17115035
|
C | T | 1 | a0001c0001t0004g0256 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1366+834C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115035 | ||||||
| chr8:17115036
|
G | A | 3 | a0001c0001t0002g0050a0001c0001t0002g0073a0001c0001t0002g0109 | 3 | HG00280.hp2 HG01978.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1366+835G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115036 | ||||||
| chr8:17115037
|
T | G | 2 | a0002c0002t0005g0186a0002c0002t0005g0190 | 2 | HG01361.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1366+836T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115037 | ||||||
| chr8:17115092
|
C | T | 128 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(125): Show | 133 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.1366+891C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115092 | ||||||
| chr8:17115118
|
CA | C | 277 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(274): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1366+933delA | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 17115118 | |||||
| chr8:17115134
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1366+933A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115134 | ||||||
| chr8:17115141
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1366+940A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115141 | ||||||
| chr8:17115453
|
C | T | 1 | a0001c0001t0002g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1367-990C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115453 | ||||||
| chr8:17115561
|
A | G | 54 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0068others(51): Show | 56 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1367-882A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115561 | ||||||
| chr8:17115708
|
A | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1367-735A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115708 | ||||||
| chr8:17115725
|
G | C | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1367-718G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115725 | ||||||
| chr8:17115855
|
T | G | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1367-588T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115855 | ||||||
| chr8:17115880
|
C | G | 3 | a0001c0001t0003g0131a0001c0001t0003g0135a0001c0001t0016g0088 | 3 | NA18969.hp1 NA18979.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1367-563C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115880 | ||||||
| chr8:17115931
|
A | G | 12 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0017others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.1367-512A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115931 | ||||||
| chr8:17115934
|
G | A | 268 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(265): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1367-509G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17115934 | ||||||
| chr8:17116197
|
G | A | 10 | a0001c0001t0006g0014a0001c0001t0006g0017a0001c0001t0006g0021others(7): Show | 10 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1367-246G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17116197 | ||||||
| chr8:17116203
|
A | G | 1 | a0001c0001t0006g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1367-240A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 12/14 | chr8 | 17116203 | ||||||
| chr8:17116750
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1524+150C>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17116750 | ||||||
| chr8:17117037
|
G | T | 1 | a0001c0001t0001g0103 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1524+437G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117037 | ||||||
| chr8:17117093
|
T | G | 1 | a0001c0001t0002g0306 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1524+493T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117093 | ||||||
| chr8:17117151
|
AT | A | 6 | a0001c0001t0002g0067a0001c0001t0002g0096a0001c0001t0002g0110others(3): Show | 6 | HG01069.hp1 HG02280.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1524+559delT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 17117151 | |||||
| chr8:17117179
|
T | G | 1 | a0001c0001t0004g0251 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1524+579T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117179 | ||||||
| chr8:17117300
|
A | C | 1 | a0001c0001t0003g0230 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1524+700A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117300 | ||||||
| chr8:17117429
|
T | C | 11 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0017others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524+829T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117429 | ||||||
| chr8:17117607
|
C | CT | 115 | a0001c0001t0001g0074a0001c0001t0001g0211a0001c0001t0001g0359others(112): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1524+1025dupT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 17117607 | |||||
| chr8:17117607
|
C | CTT | 14 | a0001c0001t0004g0257a0001c0001t0004g0260a0001c0001t0004g0268others(11): Show | 14 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1524+1024_1524+102 others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 17117607 | |||||
| chr8:17117659
|
A | C | 1 | a0001c0001t0003g0283 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1525-1048A>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117659 | ||||||
| chr8:17117695
|
G | A | 82 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0040others(79): Show | 85 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.1525-1012G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117695 | ||||||
| chr8:17117723
|
C | T | 118 | a0001c0001t0003g0002a0001c0001t0003g0005a0001c0001t0003g0056others(115): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1525-984C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117723 | ||||||
| chr8:17117770
|
G | A | 1 | a0002c0002t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1525-937G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117770 | ||||||
| chr8:17117896
|
A | G | 1 | a0001c0001t0002g0341 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1525-811A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117896 | ||||||
| chr8:17117928
|
G | A | 1 | a0001c0003t0001g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1525-779G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117928 | ||||||
| chr8:17117963
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1525-744T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17117963 | ||||||
| chr8:17118009
|
C | G | 1 | a0001c0001t0004g0255 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1525-698C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118009 | ||||||
| chr8:17118015
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0354others(8): Show | 12 | HG02257.hp2 HG02258.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1525-692G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118015 | ||||||
| chr8:17118071
|
G | A | 120 | a0001c0001t0003g0002a0001c0001t0003g0005a0001c0001t0003g0056others(117): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1525-636G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118071 | ||||||
| chr8:17118101
|
A | G | 5 | a0001c0001t0006g0020a0001c0006t0001g0237a0001c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-606A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118101 | ||||||
| chr8:17118164
|
A | G | 58 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0068others(55): Show | 60 | HG00408.hp1 HG00597.hp2 HG01346.hp1 others(57): Show |
intron_variant | MODIFIER | c.1525-543A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118164 | ||||||
| chr8:17118188
|
C | T | 119 | a0001c0001t0003g0002a0001c0001t0003g0005a0001c0001t0003g0056others(116): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1525-519C>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118188 | ||||||
| chr8:17118268
|
T | C | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1525-439T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118268 | ||||||
| chr8:17118293
|
G | A | 221 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0026others(218): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1525-414G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118293 | ||||||
| chr8:17118300
|
G | A | 1 | a0001c0001t0030g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1525-407G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118300 | ||||||
| chr8:17118446
|
A | G | 3 | a0001c0001t0001g0173a0001c0001t0029g0123a0001c0001t0030g0032 | 3 | HG02895.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1525-261A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118446 | ||||||
| chr8:17118487
|
C | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | NA18967.hp1 NA18985.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1525-220C>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118487 | ||||||
| chr8:17118565
|
G | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-142G>T | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118565 | ||||||
| chr8:17118668
|
T | C | 6 | a0001c0001t0001g0058a0001c0001t0002g0060a0001c0001t0002g0150others(3): Show | 6 | HG00438.hp2 HG01433.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1525-39T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 13/14 | chr8 | 17118668 | ||||||
| chr8:17118912
|
A | G | 1 | a0001c0001t0015g0319 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1593+137A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17118912 | ||||||
| chr8:17119006
|
T | C | 58 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0068others(55): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1593+231T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17119006 | ||||||
| chr8:17119097
|
T | C | 1 | a0001c0001t0004g0273 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1593+322T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17119097 | ||||||
| chr8:17119333
|
G | A | 1 | a0001c0001t0029g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1593+558G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17119333 | ||||||
| chr8:17119337
|
A | G | 1 | a0001c0003t0007g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1593+562A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17119337 | ||||||
| chr8:17119415
|
G | A | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1593+640G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17119415 | ||||||
| chr8:17119532
|
C | CATAG | 33 | a0001c0001t0001g0037a0001c0001t0001g0045a0001c0001t0001g0049others(30): Show | 34 | HG00099.hp1 HG00733.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.*1-714_*1-711dupTA others(2): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119532 | |||||
| chr8:17119532
|
C | CATAGATA others(1): Show |
6 | a0001c0001t0001g0051a0001c0001t0001g0232a0001c0001t0004g0244others(3): Show | 6 | HG03490.hp2 NA18953.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.*1-718_*1-711dupTA others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119532 | |||||
| chr8:17119532
|
CATAG | C | 77 | a0001c0001t0001g0058a0001c0001t0001g0070a0001c0001t0001g0087others(74): Show | 77 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.*1-714_*1-711delTA others(2): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119532 | |||||
| chr8:17119532
|
CATAGATA others(1): Show |
C | 8 | a0001c0001t0001g0346a0001c0001t0002g0084a0001c0001t0002g0085others(5): Show | 8 | HG00140.hp2 HG00639.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.*1-718_*1-711delTA others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119532 | |||||
| chr8:17119542
|
T | C | 9 | a0001c0001t0006g0014a0001c0001t0006g0017a0001c0001t0006g0020others(6): Show | 9 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.*1-746T>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17119542 | ||||||
| chr8:17119548
|
G | GATAGATA others(5): Show |
1 | a0001c0001t0001g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.*1-729_*1-728insAA others(10): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119548 | |||||
| chr8:17119552
|
G | GATAGATA others(9): Show |
2 | a0002c0002t0001g0182a0002c0005t0001g0181 | 2 | HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.*1-721_*1-720insAA others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119552 | |||||
| chr8:17119552
|
G | GATAGATA others(13): Show |
6 | a0002c0002t0001g0183a0002c0002t0001g0185a0002c0002t0001g0364others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.*1-717_*1-716insAA others(18): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119552 | |||||
| chr8:17119556
|
G | GATAA | 8 | a0001c0001t0001g0173a0001c0001t0003g0059a0001c0001t0003g0063others(5): Show | 8 | HG00408.hp2 HG02040.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.*1-729_*1-728insAA others(2): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119556 | |||||
| chr8:17119556
|
G | GATAGATA others(1): Show |
52 | a0001c0001t0001g0205a0001c0001t0001g0359a0001c0001t0003g0002others(49): Show | 54 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.*1-725_*1-724insAA others(6): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119556 | |||||
| chr8:17119556
|
G | GATAGATA others(5): Show |
24 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0355others(21): Show | 26 | HG00733.hp2 HG01069.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.*1-721_*1-720insAA others(10): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119556 | |||||
| chr8:17119556
|
G | GATAGATA others(9): Show |
15 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0286others(12): Show | 15 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.*1-717_*1-716insAA others(14): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119556 | |||||
| chr8:17119556
|
G | GATAGATA others(13): Show |
1 | a0001c0006t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.*1-713_*1-712insAA others(18): Show |
MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17119556 | |||||
| chr8:17119955
|
A | G | 1 | a0005c0012t0007g0078 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.*1-333A>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17119955 | ||||||
| chr8:17120015
|
G | A | 3 | a0001c0006t0001g0237a0001c0006t0001g0238a0001c0006t0001g0239 | 3 | HG01891.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.*1-273G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17120015 | ||||||
| chr8:17120088
|
T | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0354others(31): Show | 36 | HG01109.hp2 HG01361.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.*1-200T>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17120088 | ||||||
| chr8:17120102
|
G | A | 136 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(133): Show | 141 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.*1-186G>A | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17120102 | ||||||
| chr8:17120164
|
T | G | 1 | a0001c0001t0003g0135 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.*1-124T>G | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17120164 | ||||||
| chr8:17120218
|
T | TTTGA | 138 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0016others(135): Show | 143 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(140): Show |
intron_variant | MODIFIER | c.*1-68_*1-67insGATT | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 17120218 | |||||
| chr8:17120236
|
G | C | 3 | a0002c0002t0001g0003a0002c0002t0001g0189a0002c0002t0001g0193 | 4 | HG02572.hp1 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.*1-52G>C | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 14/14 | chr8 | 17120236 |