Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 530 | 335 | 65 | 61 | 164 | 12 | 33 | 126 | MICU3_chr8_17022238_17127642 | MICU3 | MAALR others(525): Show |
chr8 | 17022238 | 17127642 |
| a0002 | 0/0 | 530 | 29 | 28 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | MAALR others(525): Show |
chr8 | 17022238 | 17127642 |
| a0003 | 0/0 | 530 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | MAALR others(525): Show |
chr8 | 17022238 | 17127642 |
| a0004 | 0/0 | 135 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | MAALR others(130): Show |
chr8 | 17022238 | 17127642 |
| a0005 | 0/0 | 530 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | MAALR others(525): Show |
chr8 | 17022238 | 17127642 |
| a0006 | 0/0 | 371 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | MAALR others(366): Show |
chr8 | 17022238 | 17127642 |
| a0007 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | MAALR others(525): Show |
chr8 | 17022238 | 17127642 |
| a0008 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | MAALR others(525): Show |
chr8 | 17022238 | 17127642 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1590 | 308 | 62 | 54 | 152 | 11 | 29 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0001c0003 | 0/0 | 1590 | 15 | 0 | 6 | 4 | 1 | 4 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0001c0004 | 0/0 | 1590 | 6 | 0 | 0 | 6 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0001c0006 | 0/0 | 1590 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0001c0011 | 0/0 | 1590 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0001c0013 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0001c0015 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0002c0002 | 0/0 | 1590 | 25 | 24 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0002c0005 | 0/0 | 1590 | 4 | 4 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0003c0007 | 0/0 | 1590 | 2 | 0 | 2 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0004c0008 | 0/0 | 1591 | 2 | 0 | 0 | 1 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1586): Show |
chr8 | 17022238 | 17127642 | ||
| a0005c0009 | 0/0 | 1590 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0006c0010 | 0/0 | 1589 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1584): Show |
chr8 | 17022238 | 17127642 | ||
| a0007c0014 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 | ||
| a0008c0012 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | ATGGC others(1585): Show |
chr8 | 17022238 | 17127642 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3990 | 82 | 18 | 22 | 31 | 2 | 9 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0002 | 0/0 | 3990 | 84 | 12 | 10 | 47 | 3 | 12 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0003 | 0/0 | 3990 | 58 | 5 | 16 | 29 | 5 | 3 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0004 | 0/0 | 3990 | 39 | 0 | 4 | 33 | 0 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0005 | 0/0 | 3990 | 6 | 6 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0006 | 0/0 | 3990 | 7 | 7 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0008 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0009 | 0/0 | 3990 | 4 | 0 | 0 | 4 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0010 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0011 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0012 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0013 | 0/0 | 3990 | 3 | 1 | 1 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0014 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0015 | 0/0 | 3990 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0016 | 0/0 | 3990 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0018 | 0/0 | 3990 | 2 | 0 | 0 | 0 | 0 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0019 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0023 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0024 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0025 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0027 | 0/0 | 3990 | 1 | 0 | 0 | 0 | 1 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0028 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0029 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0001t0030 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0003t0001 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0003t0002 | 0/0 | 3990 | 7 | 0 | 4 | 0 | 1 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0003t0007 | 0/0 | 3990 | 3 | 0 | 0 | 3 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0003t0011 | 0/0 | 3990 | 2 | 0 | 0 | 0 | 0 | 2 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0003t0020 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0003t0022 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0004t0001 | 0/0 | 3990 | 2 | 0 | 0 | 2 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0004t0002 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0004t0004 | 0/0 | 3990 | 3 | 0 | 0 | 3 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0006t0001 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0011t0001 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0013t0003 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0001c0015t0021 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0002c0002t0001 | 0/0 | 3990 | 17 | 17 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0002c0002t0003 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0002c0002t0005 | 0/0 | 3990 | 2 | 1 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0002c0002t0008 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0002c0002t0017 | 0/0 | 3990 | 2 | 2 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0002c0005t0001 | 0/0 | 3990 | 4 | 4 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0003c0007t0002 | 0/0 | 3990 | 2 | 0 | 2 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0004c0008t0002 | 0/0 | 3991 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3986): Show |
chr8 | 17022238 | 17127642 |
| a0004c0008t0004 | 0/0 | 3991 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3986): Show |
chr8 | 17022238 | 17127642 |
| a0005c0009t0026 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0006c0010t0001 | 0/0 | 3989 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3984): Show |
chr8 | 17022238 | 17127642 |
| a0007c0014t0007 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| a0008c0012t0002 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | GTTCT others(3985): Show |
chr8 | 17022238 | 17127642 |
| actghapid | grch38/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 |
| 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 |
| 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 |
| 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 |
| 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 | 1 | 0 | 0 | 1 | 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 |
| a0001c0011t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0013t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0001c0015t0021g0263 | 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 |
| a0004c0008t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0004c0008t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0005c0009t0026g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0006c0010t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0007c0014t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MICU3_chr8_17022238_17127642 | MICU3 | chr8 | 17022238 | 17127642 |
| a0008c0012t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 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 | c0011 | 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 | a0005 | c0009 | 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 | c0015 | 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 | a0004 | c0008 | 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 | a0006 | c0010 | 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 | c0013 | 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 | a0007 | c0014 | 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 | a0008 | c0012 | 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 | a0004 | c0008 | 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 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:17027501 | C | CG | 1 | a0004 | 2 | HG03927.hp1 NA19076.hp2 |
frameshift_variant | HIGH | c.228dupG | p.Leu77fs | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 1/15 | 271/3990 | 229/1593 | 77/530 | INFO_REALIGN_3_PRIME | chr8 | 17027501 | ||
| chr8:17027553 | G | C | 2 | a0002 a0005 |
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 | a0005 | 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 | a0008 | 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 | a0007 | 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 | |||
| chr8:17104474 | CT | C | 1 | a0006 | 1 | NA18963.hp1 | frameshift_variant | HIGH | c.1071delT | p.Phe357fs | MICU3 | ENSG00000155970.12 | transcript | ENST00000318063.10 | protein_coding | 10/15 | 1113/3990 | 1071/1593 | 357/530 | INFO_REALIGN_3_PRIME | chr8 | 17104474 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:17027369 | G | T | 1 | a0001c0015 | 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 | a0001c0003 a0007c0014 |
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 | a0001c0013 | 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 | a0001c0011 a0002c0005 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(17): 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 | a0001c0001t0029 a0001c0001t0030 |
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 | a0001c0001t0003 a0001c0013t0003 a0002c0002t0003 |
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 | a0001c0001t0008 a0001c0001t0014 a0002c0002t0008 |
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 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0025 |
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 | a0001c0001t0011 a0001c0003t0007 a0001c0003t0011 others(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 | a0001c0001t0005 a0002c0002t0005 |
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 | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(15): 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 | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(17): 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 | a0005c0009t0026 | 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 | a0001c0015t0021 | 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 | 11 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0019 others(8): 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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0005g0027 others(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 | 176 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(173): 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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0003g0357 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | 46 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0002g0252 others(43): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
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 | a0001c0003t0002g0200 a0001c0003t0002g0201 a0001c0003t0002g0202 others(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 | 42 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(39): 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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0005 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0013t0003g0199 | 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 | 214 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(211): 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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0286 a0001c0001t0003g0283 a0001c0001t0003g0284 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | 44 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(41): 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 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
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 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
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 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
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 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
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 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0074 others(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 | 88 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0058 others(85): 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 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0002c0002t0008g0177 |
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 | a0002c0002t0001g0003 a0002c0002t0001g0182 a0002c0002t0001g0183 others(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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 others(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 | a0001c0001t0001g0351 a0001c0001t0001g0353 a0001c0001t0004g0279 others(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 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0008g0011 others(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 | a0001c0001t0001g0164 a0001c0001t0003g0165 a0001c0001t0003g0357 |
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 | a0002c0002t0001g0178 a0002c0002t0001g0191 a0002c0002t0001g0192 others(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 | a0002c0002t0001g0191 a0002c0002t0001g0192 a0002c0002t0001g0193 others(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 | 179 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(176): 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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0005g0027 others(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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | 178 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(175): 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 | 176 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(173): 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 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
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 | a0001c0001t0006g0014 a0001c0001t0006g0017 a0001c0001t0025g0018 others(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 | 44 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(41): 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 | 44 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(41): 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 | a0001c0001t0002g0050 a0001c0001t0002g0073 |
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 | a0002c0002t0001g0003 a0002c0002t0001g0179 a0002c0002t0001g0182 others(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 | 203 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(200): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
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 | 44 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(41): 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 | 44 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(41): 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 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0051 |
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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | 176 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(173): 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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | 44 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(41): 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 | 44 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(41): 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 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
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 | a0001c0011t0001g0019 | 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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0286 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(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 | a0001c0011t0001g0019 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0004g0242 a0001c0001t0004g0251 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0070 |
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 | 44 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(41): 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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0012g0029 a0001c0001t0012g0030 a0001c0001t0012g0031 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
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 | a0002c0002t0001g0182 a0002c0002t0001g0183 a0002c0002t0001g0185 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0003t0002g0039 a0001c0003t0002g0054 a0001c0003t0002g0200 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0004g0253 a0001c0001t0004g0254 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0297 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 others(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 | a0001c0001t0001g0219 a0001c0001t0018g0362 |
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 | a0002c0002t0001g0003 a0002c0002t0001g0178 a0002c0002t0001g0179 others(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 | a0001c0001t0005g0218 a0001c0001t0010g0227 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | a0001c0003t0007g0036 a0001c0003t0007g0047 a0007c0014t0007g0078 |
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 | a0001c0001t0002g0050 a0001c0001t0002g0073 |
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 | a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0001g0321 a0001c0001t0002g0345 a0001c0001t0011g0322 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0173 a0001c0001t0001g0205 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0073 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | a0002c0002t0001g0003 a0002c0002t0001g0178 a0002c0002t0001g0179 others(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 | a0001c0001t0002g0127 a0001c0001t0002g0129 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0002c0002t0001g0003 a0002c0002t0001g0179 a0002c0002t0001g0182 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0002c0002t0001g0003 a0002c0002t0001g0179 a0002c0002t0001g0182 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0286 a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0004c0008t0002g0320 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
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 | a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0070 a0001c0001t0002g0001 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0205 others(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 | 137 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(134): 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 | 137 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(134): 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 | 170 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(167): 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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0001g0173 a0001c0001t0006g0020 a0001c0006t0001g0237 others(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 | a0001c0001t0001g0079 a0001c0001t0003g0081 a0001c0001t0004g0080 |
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 | a0001c0001t0002g0360 a0001c0001t0002g0361 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0002c0002t0001g0178 a0002c0002t0008g0172 a0002c0002t0008g0176 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | 60 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(57): 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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0008c0012t0002g0280 | 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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0216 a0001c0001t0001g0219 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0011t0001g0019 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0297 others(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 | 363 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(360): 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 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0002g0348 others(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 | 168 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(165): 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 | a0001c0001t0001g0326 a0001c0004t0001g0209 a0001c0004t0002g0208 others(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 | a0002c0002t0008g0172 a0002c0002t0008g0176 a0002c0002t0008g0177 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0002c0002t0001g0003 a0002c0002t0001g0178 a0002c0002t0001g0179 others(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 | a0001c0001t0001g0228 a0001c0001t0001g0232 a0001c0001t0013g0224 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0236 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0297 others(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 | 215 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): 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 | a0002c0002t0001g0192 a0002c0002t0001g0195 a0002c0002t0001g0196 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0070 a0001c0001t0002g0001 others(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 | a0001c0001t0002g0360 a0001c0001t0002g0361 |
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 | 83 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0048 others(80): 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 | a0001c0001t0001g0173 a0001c0001t0001g0293 a0001c0001t0001g0297 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0212 a0001c0001t0001g0326 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0286 a0001c0001t0006g0015 others(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 | a0001c0001t0006g0014 a0002c0002t0001g0178 a0002c0002t0001g0179 others(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 | a0001c0001t0025g0018 a0002c0002t0001g0003 a0002c0002t0001g0191 others(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 | a0002c0002t0008g0172 a0002c0002t0008g0176 |
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 | a0001c0003t0002g0039 a0001c0003t0002g0054 a0001c0003t0002g0200 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0173 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0173 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0173 a0001c0001t0001g0205 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0125 a0001c0001t0001g0126 others(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 | a0001c0001t0002g0329 a0001c0001t0002g0330 a0001c0001t0002g0331 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0173 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | 168 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(165): 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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0002g0360 a0001c0001t0002g0361 |
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 | a0002c0002t0008g0172 a0002c0002t0008g0176 a0002c0002t0008g0177 |
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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | 94 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0173 others(91): 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 | a0001c0001t0001g0004 a0001c0001t0001g0173 a0001c0001t0001g0205 others(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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | 215 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): 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 | 170 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(167): 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 | 215 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): 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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0216 |
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 | 89 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0173 others(86): 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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0003g0002 a0001c0001t0003g0149 |
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 | 215 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): 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 | 45 | a0001c0001t0001g0082 a0001c0001t0002g0252 a0001c0001t0002g0275 others(42): 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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0005g0027 others(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 | a0008c0012t0002g0280 | 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 | a0001c0001t0003g0002 a0001c0001t0003g0146 a0001c0001t0003g0149 |
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 | 89 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0173 others(86): 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 | a0001c0001t0001g0286 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0121 others(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 | 214 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(211): 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 | 43 | a0001c0001t0001g0082 a0001c0001t0002g0252 a0001c0001t0002g0275 others(40): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
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 | a0002c0002t0001g0003 a0002c0002t0001g0178 a0002c0002t0001g0179 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0002c0002t0001g0183 a0002c0002t0001g0185 |
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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | a0008c0012t0002g0280 | 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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0001g0121 a0001c0001t0003g0059 a0001c0001t0003g0063 others(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 | a0001c0001t0004g0009 a0001c0001t0004g0248 a0001c0001t0004g0266 |
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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | 188 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0026 others(185): 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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0220 |
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 | 188 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(185): 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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | a0001c0001t0002g0060 a0001c0001t0002g0150 a0001c0001t0002g0153 others(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 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0313 |
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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0008g0011 a0002c0002t0008g0172 a0002c0002t0008g0176 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0220 |
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 | a0002c0002t0001g0191 a0002c0002t0001g0192 a0002c0002t0001g0193 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0167 a0001c0003t0002g0039 a0001c0003t0002g0054 others(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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 others(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 | a0001c0001t0008g0011 a0002c0002t0008g0172 a0002c0002t0008g0176 others(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 | 227 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(224): 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 | a0001c0001t0001g0326 a0001c0001t0001g0351 a0001c0004t0001g0209 others(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 | 227 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(224): 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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | 363 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(360): 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 | a0001c0001t0002g0360 a0001c0001t0002g0361 |
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 | a0008c0012t0002g0280 | 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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0006t0001g0237 a0001c0006t0001g0239 |
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 | 58 | a0001c0001t0001g0082 a0001c0001t0002g0252 a0001c0001t0002g0275 others(55): 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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | 58 | a0001c0001t0001g0082 a0001c0001t0002g0252 a0001c0001t0002g0275 others(55): 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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0173 a0001c0001t0001g0205 others(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 | a0001c0001t0002g0252 a0001c0001t0004g0068 a0001c0001t0004g0265 |
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 | 87 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0122 others(84): 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 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0297 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0173 a0001c0001t0001g0205 others(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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | 231 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(228): 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 | a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 others(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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0070 a0001c0001t0002g0001 |
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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0045 |
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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0312 a0001c0001t0002g0317 |
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 | 51 | a0001c0001t0001g0082 a0001c0001t0002g0252 a0001c0001t0002g0275 others(48): 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 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | 50 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(47): 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 | 50 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(47): 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 | 50 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(47): 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 | a0001c0001t0002g0067 a0001c0001t0002g0096 a0001c0001t0002g0110 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0002g0290 a0001c0001t0003g0288 a0001c0001t0003g0291 |
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 | a0001c0001t0001g0232 a0001c0001t0018g0233 |
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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | 158 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(155): 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 | 158 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(155): 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 | a0001c0001t0004g0247 a0001c0001t0004g0250 a0001c0001t0004g0256 others(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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0004g0343 a0001c0001t0016g0338 |
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 | a0002c0002t0001g0178 a0002c0002t0008g0172 a0002c0002t0008g0176 others(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 | 56 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(53): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
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 | 284 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(281): 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 | a0001c0001t0003g0135 a0001c0001t0016g0088 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | 144 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0082 others(141): 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 | a0001c0001t0004g0253 a0001c0001t0004g0254 |
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 | a0001c0001t0001g0228 a0001c0001t0001g0232 a0001c0001t0013g0224 others(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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0001g0359 a0001c0001t0002g0360 a0001c0001t0002g0361 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
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 | 284 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(281): 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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0002g0013 others(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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | 95 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(92): 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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | 213 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0082 others(210): 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 | a0001c0001t0002g0141 a0001c0001t0003g0002 a0001c0001t0003g0057 others(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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | 59 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(56): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0236 others(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 | a0001c0001t0004g0253 a0001c0001t0004g0254 |
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 | 58 | a0001c0001t0001g0082 a0001c0001t0002g0252 a0001c0001t0002g0275 others(55): 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 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0058 a0001c0001t0003g0056 |
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 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0003g0357 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | a0001c0001t0011g0322 a0002c0002t0001g0003 a0002c0002t0001g0178 others(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 | 191 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0070 others(188): 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 | 59 | a0001c0001t0001g0082 a0001c0001t0002g0034 a0001c0001t0002g0252 others(56): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
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 | 57 | a0001c0001t0002g0252 a0001c0001t0002g0275 a0001c0001t0002g0277 others(54): 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 | a0001c0001t0003g0059 a0001c0001t0003g0063 a0001c0001t0003g0097 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0001g0293 others(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 | 180 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0074 others(177): 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 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0021 a0001c0001t0006g0025 others(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 | a0001c0001t0008g0011 a0002c0002t0008g0172 a0002c0002t0008g0176 others(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 | a0001c0001t0014g0006 a0001c0001t0014g0217 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0168 others(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 | a0001c0003t0007g0036 a0001c0003t0007g0038 a0001c0003t0007g0047 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0004g0253 a0001c0001t0004g0254 |
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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0003t0001g0089 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0211 others(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 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0222 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0121 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0353 a0001c0001t0002g0296 a0001c0001t0002g0349 others(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 | a0001c0001t0001g0223 a0001c0001t0003g0215 |
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 | a0001c0001t0003g0148 a0001c0001t0004g0343 a0001c0001t0016g0338 |
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 | a0001c0001t0002g0341 a0001c0001t0006g0025 a0001c0001t0012g0029 others(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 | a0001c0001t0001g0355 a0001c0001t0006g0017 a0001c0001t0025g0018 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0354 a0001c0001t0010g0022 others(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 | a0001c0001t0001g0356 a0001c0001t0005g0027 a0001c0001t0006g0015 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0286 a0001c0001t0006g0021 others(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 | a0001c0011t0001g0019 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0281 others(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 | a0001c0001t0006g0014 a0001c0001t0025g0018 |
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 | a0001c0001t0001g0119 a0001c0001t0002g0114 a0001c0001t0002g0132 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0168 others(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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0011g0322 a0002c0002t0001g0003 a0002c0002t0001g0179 others(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 | a0001c0001t0001g0167 a0001c0003t0011g0061 |
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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0002c0002t0001g0003 a0002c0002t0001g0179 a0002c0002t0001g0182 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0126 a0001c0001t0001g0359 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | 290 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(287): 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 | a0001c0001t0001g0353 a0006c0010t0001g0352 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0236 others(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 | 286 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(283): 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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0117 a0001c0001t0002g0067 a0001c0001t0002g0096 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0013g0161 |
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 | a0001c0001t0003g0288 a0001c0001t0003g0292 |
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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0313 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | 58 | a0001c0001t0001g0082 a0001c0001t0002g0252 a0001c0001t0002g0275 others(55): 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 | a0001c0001t0001g0058 a0001c0001t0001g0079 a0001c0001t0001g0094 others(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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0236 a0001c0001t0002g0324 a0001c0001t0005g0234 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | 282 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(279): 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 | a0001c0001t0002g0324 a0001c0001t0005g0027 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0003g0059 others(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 | 160 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0082 others(157): 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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0141 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0141 others(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 | 360 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(357): 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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | 60 | a0001c0001t0001g0082 a0001c0001t0002g0252 a0001c0001t0002g0275 others(57): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0011g0322 others(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 | a0001c0001t0006g0014 a0001c0001t0025g0018 |
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 | 283 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(280): 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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0013g0161 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | 100 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0205 others(97): 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 | a0001c0001t0003g0090 a0001c0001t0003g0136 |
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 | 93 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0205 others(90): 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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0074 others(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 | 287 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(284): 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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0013t0003g0199 | 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 | a0001c0001t0014g0006 a0001c0001t0014g0217 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0154 a0001c0001t0002g0155 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0141 a0001c0001t0002g0154 others(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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | 72 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0049 others(69): 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 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0004g0068 a0001c0001t0004g0256 a0001c0001t0004g0262 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0313 a0001c0001t0001g0337 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0087 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0298 a0001c0001t0003g0357 a0001c0001t0005g0027 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0011g0322 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0011g0322 others(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 | a0001c0001t0001g0173 a0001c0001t0002g0132 a0001c0001t0002g0141 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0219 a0001c0001t0018g0233 a0001c0001t0018g0362 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0013g0161 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | a0001c0001t0002g0318 a0001c0001t0015g0319 |
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 | a0001c0001t0002g0132 a0001c0001t0002g0154 a0001c0001t0002g0155 others(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 | 360 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(357): 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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0002g0252 a0001c0001t0004g0265 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | 155 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0167 others(152): 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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(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 | a0001c0001t0014g0006 a0001c0001t0014g0217 |
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 | 179 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0074 others(176): 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 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(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 | 177 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0074 others(174): 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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0002g0127 a0001c0001t0002g0129 |
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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0014g0006 a0001c0001t0014g0217 |
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 | a0001c0001t0002g0308 a0001c0001t0002g0314 a0001c0001t0002g0327 others(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 | 59 | a0001c0001t0001g0082 a0001c0001t0001g0167 a0001c0001t0002g0252 others(56): 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 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0227 |
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 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | 176 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0074 others(173): 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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0003t0007g0036 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0002g0275 a0001c0001t0004g0255 a0001c0001t0004g0259 others(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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0141 a0001c0001t0002g0154 others(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 | a0001c0001t0004g0247 a0001c0001t0004g0250 |
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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | 56 | a0001c0001t0001g0082 a0001c0001t0002g0252 a0001c0001t0002g0275 others(53): 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 | a0001c0001t0004g0242 a0001c0001t0004g0251 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0002c0002t0001g0182 a0002c0002t0001g0183 a0002c0002t0001g0185 others(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 | a0001c0001t0001g0297 a0001c0001t0001g0311 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | a0001c0001t0003g0069 a0001c0001t0003g0072 a0001c0001t0003g0076 others(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 | 284 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(281): 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 | 175 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0082 others(172): 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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0011g0322 others(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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0006g0014 a0001c0001t0025g0018 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | 284 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(281): 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 | 179 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0074 others(176): 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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0002g0141 a0001c0001t0003g0002 a0001c0001t0003g0057 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0015t0021g0263 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0021 |
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 | 284 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(281): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0011g0322 others(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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0300 a0001c0001t0002g0141 a0001c0001t0003g0002 others(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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | 130 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0074 others(127): 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 | a0001c0001t0014g0006 a0001c0001t0014g0217 |
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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0018g0233 a0001c0001t0018g0362 |
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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0236 others(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 | a0001c0001t0002g0066 a0001c0001t0002g0071 a0001c0001t0002g0142 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0073 |
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 | 56 | a0001c0001t0001g0082 a0001c0001t0002g0252 a0001c0001t0002g0275 others(53): 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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0002c0002t0005g0186 a0002c0002t0005g0190 |
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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0220 |
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 | a0001c0001t0002g0360 a0001c0001t0002g0361 |
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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0014g0006 a0001c0001t0014g0217 |
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 | 291 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(288): 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 | a0001c0001t0001g0004 a0001c0001t0001g0173 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | 290 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(287): 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 | a0008c0012t0002g0280 | 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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0001c0001t0001g0219 a0001c0001t0001g0228 a0001c0001t0001g0232 |
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 | a0001c0001t0002g0252 a0001c0001t0004g0265 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0003g0002 a0001c0001t0003g0057 a0001c0001t0003g0059 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0049 others(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 | a0001c0001t0004g0255 a0001c0001t0004g0259 a0001c0001t0004g0260 others(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 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0227 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0121 others(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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 others(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 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0227 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0236 others(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 | a0003c0007t0002g0064 a0003c0007t0002g0106 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0170 a0001c0001t0001g0173 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0228 a0001c0001t0003g0069 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0223 a0001c0001t0003g0091 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0220 a0001c0001t0005g0226 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0359 a0001c0001t0002g0159 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0167 others(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 | 55 | a0001c0001t0001g0082 a0001c0001t0001g0323 a0001c0001t0001g0354 others(52): 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 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0001g0293 others(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 | a0001c0001t0002g0252 a0001c0001t0003g0283 a0001c0001t0004g0257 others(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 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
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 | 364 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(361): 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 | a0001c0001t0002g0308 a0001c0001t0002g0314 a0001c0001t0002g0327 others(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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 others(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 | a0001c0001t0003g0215 a0001c0001t0003g0288 a0001c0001t0003g0291 others(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 | a0001c0001t0003g0002 a0001c0001t0003g0057 a0001c0001t0003g0059 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(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 | a0005c0009t0026g0184 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0013g0161 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0115 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | 215 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): 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 | a0001c0001t0003g0135 a0001c0001t0016g0088 |
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 | a0001c0001t0002g0066 a0001c0001t0002g0142 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0004g0256 a0001c0001t0004g0257 a0001c0001t0004g0268 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | 207 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(204): 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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | a0004c0008t0002g0320 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0003g0131 a0001c0001t0003g0135 a0001c0001t0016g0088 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | 59 | a0001c0001t0001g0082 a0001c0001t0001g0167 a0001c0001t0002g0252 others(56): 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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0008g0011 others(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 | 213 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(210): 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 | a0001c0001t0001g0236 a0001c0001t0005g0234 a0001c0001t0005g0235 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0005g0218 a0001c0001t0005g0225 a0001c0001t0005g0226 |
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 | a0001c0001t0004g0257 a0001c0001t0004g0268 a0001c0001t0004g0273 others(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 | 209 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(206): 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 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0315 others(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 | a0002c0002t0017g0188 a0002c0002t0017g0194 |
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 | 135 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0082 others(132): 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 | a0001c0001t0014g0006 a0001c0001t0014g0217 |
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 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 others(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 | 215 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(212): 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 | a0001c0001t0001g0070 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0003g0002 a0001c0001t0003g0057 a0001c0001t0003g0059 others(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 | 57 | a0001c0001t0001g0082 a0001c0001t0001g0167 a0001c0001t0002g0252 others(54): 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 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0008g0011 others(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 | 58 | a0001c0001t0001g0082 a0001c0001t0001g0167 a0001c0001t0002g0252 others(55): 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 | a0001c0001t0003g0124 a0001c0001t0003g0152 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0236 others(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 | 128 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0082 others(125): 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 | a0001c0011t0001g0019 | 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 | 170 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0026 others(167): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0236 others(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 | 128 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0082 others(125): 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 | 124 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0082 others(121): 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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0013g0161 others(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 | 123 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0082 others(120): 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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0003g0002 a0001c0001t0003g0057 a0001c0001t0003g0059 others(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 | a0001c0001t0010g0022 a0001c0001t0010g0023 a0001c0001t0010g0227 |
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 | 214 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0082 others(211): 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 | 58 | a0001c0001t0001g0082 a0001c0001t0001g0167 a0001c0001t0002g0252 others(55): 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 | a0001c0001t0001g0355 a0001c0001t0001g0356 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0002g0360 a0001c0001t0002g0361 |
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 | 296 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(293): 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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0002c0002t0001g0191 others(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 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 |
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 | a0001c0001t0008g0011 a0002c0002t0001g0178 a0002c0002t0008g0172 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | 295 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(292): 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 | 164 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0082 others(161): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0168 a0001c0001t0001g0170 others(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 | 58 | a0001c0001t0001g0082 a0001c0001t0001g0167 a0001c0001t0002g0252 others(55): 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 | 209 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0082 others(206): 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 | a0001c0001t0001g0074 a0001c0001t0001g0359 a0001c0001t0002g0360 others(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 | 295 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(292): 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 | a0001c0001t0001g0048 a0001c0001t0002g0001 a0001c0001t0002g0162 others(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 | a0001c0001t0003g0002 a0001c0001t0003g0057 a0001c0001t0003g0059 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0236 others(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 | 57 | a0001c0001t0001g0082 a0001c0001t0001g0167 a0001c0001t0002g0252 others(54): 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 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | 57 | a0001c0001t0001g0082 a0001c0001t0001g0167 a0001c0001t0002g0252 others(54): 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 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0219 a0001c0001t0001g0232 |
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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | 55 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0068 others(52): 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 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0044 |
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 | a0001c0001t0001g0300 a0001c0001t0001g0315 a0001c0001t0001g0316 others(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 | a0001c0001t0002g0141 a0001c0001t0002g0330 |
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 | a0002c0002t0001g0197 a0002c0002t0017g0188 a0002c0002t0017g0194 |
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 | a0001c0001t0002g0050 a0001c0001t0002g0073 a0001c0001t0002g0109 |
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 | a0002c0002t0005g0186 a0002c0002t0005g0190 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | 278 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(275): 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 | 55 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0068 others(52): 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 | a0001c0001t0003g0131 a0001c0001t0003g0135 a0001c0001t0016g0088 |
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 | a0001c0001t0006g0014 a0001c0001t0006g0015 a0001c0001t0006g0017 others(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 | 269 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(266): 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 | a0001c0001t0006g0014 a0001c0001t0006g0017 a0001c0001t0006g0021 others(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 | a0001c0001t0002g0067 a0001c0001t0002g0096 a0001c0001t0002g0110 others(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 | a0001c0001t0006g0014 a0001c0001t0006g0015 a0001c0001t0006g0017 others(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 | 116 | a0001c0001t0001g0074 a0001c0001t0001g0211 a0001c0001t0001g0359 others(113): 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 | a0001c0001t0004g0257 a0001c0001t0004g0260 a0001c0001t0004g0268 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0040 others(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 | 119 | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0056 others(116): 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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0354 others(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 | 121 | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0056 others(118): 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 | a0001c0001t0006g0020 a0001c0006t0001g0237 a0001c0006t0001g0238 others(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 | 59 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0068 others(56): 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 | 120 | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0056 others(117): 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 | 222 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0026 others(219): 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 | a0001c0001t0001g0173 a0001c0001t0029g0123 a0001c0001t0030g0032 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0293 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0058 a0001c0001t0002g0060 a0001c0001t0002g0150 others(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 | 59 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0068 others(56): 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 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0001c0001t0001g0049 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0232 a0001c0001t0004g0244 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0346 a0001c0001t0002g0084 a0001c0001t0002g0085 others(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 | a0001c0001t0006g0014 a0001c0001t0006g0017 a0001c0001t0006g0020 others(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 | a0002c0002t0001g0182 a0002c0005t0001g0181 |
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 | a0002c0002t0001g0183 a0002c0002t0001g0185 a0002c0002t0001g0364 others(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 | a0001c0001t0001g0173 a0001c0001t0003g0059 a0001c0001t0003g0063 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0359 a0001c0001t0003g0002 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0074 a0001c0001t0001g0355 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0286 others(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 | a0007c0014t0007g0078 | 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 | a0001c0006t0001g0237 a0001c0006t0001g0238 a0001c0006t0001g0239 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0205 a0001c0001t0001g0354 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | a0002c0002t0001g0003 a0002c0002t0001g0189 a0002c0002t0001g0193 |
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 |